V. Jeyanthi and S. Kanimozhi*

P.G. & Research Department of Microbiology, Asan Memorial College of Arts and Science, Chennai, India.

ABSTRACT

Plant growth-promoting rhizobacteria (PGPR) are naturally occurring soil bacteria that colonize plant roots, which is an important environment for plant microbe interactions. PGPR have attracted special attention for their ability to enhance productivity, sustainability and profitability when food security and rural livelihood are a key priority. Chemical fertilizers used in agriculture and pathogenic microorganisms attacking plants show harmful impact on the ecosystem. The potentiality of PGPR offers an attractive way to replace the use of chemical fertilizers, pesticides and other supplements. PGPR affect plant growth and development directly or indirectly, either by releasing plant growth regulators or other biologically active substances, and uptake of nutrients through fixation and mobilization, reducing harmful effects of pathogenic microorganisms on plants and by employing multiple mechanisms of action. Besides they play an important role in soil fertility. This review intends to elucidate the diverse mechanisms of plant growth promoting rhizobacteria in promoting crop production and developing sustainable agriculture.

Keywords: PGPR, Siderophore, Phytohormone, Antibiosis, ISR.

INTRODUCTION

Agriculture, the science or the practice of cultivating plants, animals and other life forms, is certainly one of the factors that boost human civilization and development. Development of agriculture is an evolutionary process that ultimately transformed plants from being independent, wild progenitors into fully dependent, domesticated cultivars with the concomitant evolution of agricultural economics (Zeder, 20091). This relationship between humans, the earth and food sources further confirm soil as the foundation of agriculture, and microbes play a vital role in sustaining our natural ecosystems. Soil, the dynamic and valuable natural resource harbouring a vast collection of microorganisms, is vital for the production of food and fibre, in addition involved in the maintenance of global nutrient balance and ecosystem function (Bishnoi, 20152). Agricultural sustainability, food security and energy renewability depends on a healthy and fertile soil. Imbalance in nitrogen  cycling, nutritional status, physical and biological properties of soil, incidence of pests and diseases, fluctuating climatic factors and abiotic stresses are the interlinked contributing factors for reduced agricultural productivity (Gopalakrishnan, 20153). The existing approaches to agriculture include the use of chemical fertilizers, herbicides, fungicides, insecticides. These fertilizers have become essential components of modern agriculture because they provide essential plant nutrients such as nitrogen, phosphorus and potassium. However, the overuse of fertilizers can cause unanticipated environmental impacts (Shenoy et al., 20014; Adesemoye et al., 20095) and encounter problems such as, development of resistance by pathogen to fungicides and rapid degradation of the chemicals.

Towards a sustainable agricultural vision, crops produced need to be equipped with disease resistance, salt tolerance, drought tolerance, heavy metal stress tolerance and better nutritional value. To accomplish the above desired crop properties, one possibility is to use soil microorganisms. The main functions of these bacteria are (1) to supply nutrients to crops, (2) to stimulate plant growth, (3) to control or inhibit the activity of plant pathogens, (4) to improve soil structure, and (5) bioaccumulation or microbial leaching of inorganics (Hayat, 20106).  More recently, bacteria have also been used in soil for the mineralization of organic pollutants, i.e. bioremediation of polluted soils (Burd et al., 20007; Zhuang et al., 20078; Zaidi et al., 20089). Multiple types of biological interactions between microorganisms and plants take place in the soil (Gouda et al., 201810). This review provides an environment friendly approach to increase crop production and health, development of sustainable agriculture as well as fertility of soil exploiting plant growth promoting rhizobacteria

Rhizosphere
Rhizosphere is a well characterized ecological niche comprising volume of soil surrounding plant roots with highest bacterial population that are influenced by root exudates as defined by Hiltner (190411). Diverse communities of beneficial soil microorganisms are associated with the root systems of all higher plants (Khalid et al., 200612). It is quiet common that the bacterial population in the rhizosphere are 100–1,000 times higher than the surrounding soil, also known as the bulk soil which are not penetrated by plant roots and have lower microbial communities within it. In contrast the rhizosphere is heavily influenced by microbes that possess metabolic versatility to adapt and utilize root exudates efficiently. Also, 15% of the root surface is covered by microbial populations belonging to several bacterial species (Jha et al., 201013; Govindasamy et al., 201114). Plant roots synthesize, accumulate, and secrete a diverse array of compounds. The exudation of a wide range of chemical compounds modifies the chemical and physical properties of the soil and thus, regulates the structure of soil microbial community in the immediate vicinity of root surface (Dakora and Phillips, 200215). Root exudates include the releasing of ions, oxygen, water, and organic compounds, such as sugars, organic acids, amino acids, enzymes, growth factors and others. The composition of these exudates is dependent upon the physiological status and species of plants and microorganisms (Kang et al., 201016). Moreover, these exudates also promote the plant-beneficial symbiotic interactions and inhibit the growth of the competing plant species (Nardi et al., 200017; Haas and Defago, 200518). The sugars, amino acids, flavanoids, proteins, and fatty acids secreted by plant roots help to structure the associated soil microbiome (Badri et al., 200919; Dennis et al., 201020; Doornbos et al., 201221). The quantity and composition of root exudates vary with plant developmental stage and the proximity to neighbouring species (Chaparro et al., 201222).  From these plant-derived small organic molecules, a fraction is further metabolized by microorganisms in the surrounding area as carbon and nitrogen sources, and some microbe-oriented molecules are subsequently re-taken up by plants for growth and development (Kang et al., 201016).

Apart from the rhizosphere, the rhizoplane is the root surface including the strongly adhering soil particles while the root itself is a component of the system, because many micro-organisms (like endophytes) also colonize the root tissues (Barea et al., 200523). Plant rhizospheric region is a dynamic and versatile environment of acute plant microbe interactions for tackling essential macro and micro nutrients from a confined nutrient pool. They play a significant role both under stressed and normal conditions for improving plant growth and developmental processes (Zahir et al., 200424; Glick et al., 200725). Currently, it is recognized that the rhizosphere microbiome harbours thousands of different bacterial, archaeal, viruses, fungal and other eukaryotic taxa (Lagos et al., 201526). Though numerous microorganisms coexist in the rhizospheric region, bacteria are the abundant among them. The bacteria colonizing the rhizosphere habitat are called rhizobacteria (Kloepper et al., 199127) which influence the plant growth in a most significant manner (Uren, 200728). Rhizospheric bacteria participate in the geochemical cycling of nutrients especially carbon, nitrogen, phosphorus and micronutrients as iron, manganese, zinc and copper, and determine their availability for plants and soil microbial community Plant carbon photosynthates allocated to the root and rhizosphere are key microbial activities important for plant nutrition such as organic matter decomposition, phosphate  solubilisation, nitrogen  fixation, mycorrhizal nutrient transport and bio control of root pests (Larsen et al., 201529).

Plants only prefer those bacteria contributing close to  their relevance by releasing sugars, amino acids, organic acids, vitamins, enzymes and organic or inorganic ions through roots exudates (Gray and Smith, 200530; Gopalakrishnan, 20153) producing a environment where diversity is low (Das et al., 201331). In spite of the numerous bacteria in soil, three types of interaction takes place between rhizosphere bacteria and plants which are the positive, negative and neutral interactions. Mostly, commensalism is exhibited where a harmless interaction with the host plants is exhibited without affecting the plant physiology, whereas in negative interaction phototoxic substances are produced by rhizosphere  bacteria. Positive interaction exerts a positive growth. Multiple microbial interactions enhance bio control in the rhizosphere region (Whipps, 200132). In this regard, the use of naturally occurring and environmentally safe products such as plant growth-promoting rhizobacteria (PGPR) has found a potential role in developing sustainable systems in crop production.

Plant growth promoting rhizobacteria (PGPR)
Plant growth promoting rhizobacteria (PGPR), a diverse group of soil bacteria, are key components of soil plant systems, where they are engaged in an intense network of interactions in the rhizosphere, thus affecting the plant growth and yield. It was Kloepper and Schroth (198133), who coined the term plant growth promoting rhizobacteria for these beneficial microbes. Numerous species of soil bacteria which flourish in the rhizosphere of plants, but which may grow in, on, or around plant tissues, and stimulate plant growth by a plethora of mechanisms (Vessey, 200334). PGPR’s are the potential tools for sustainable agriculture and trend for the future; they not only ensure the availability of essential nutrients to plants but also enhance the nutrient use efficiency (Khalid et al., 200935). The beneficial effects of PGPR involve boosting key physiological processes, including water and nutrient uptake, photosynthesis, and source-sink relationships that promote growth and development (Illangumaran and Smith, 201736). One of the mechanisms by which bacteria are adsorbed onto soil particles is by ion exchange. A soil is said to be naturally fertile when the soil organisms are releasing inorganic nutrients from the organic reserves at a rate sufficient to sustain rapid plant growth (Goswami et al., 201637). Gray and Smith (200530) have shown that the PGPR associations range in the degree of bacterial proximity to the root and intimacy of association. The three distinct characteristics of  PGPR are  they must be able to colonize the root, they must survive and multiply in microhabitats associated with the root surface, in competition with other microbiota, at least for the time needed to express their plant  promotion/protection activities and they must promote plant growth (Kloepper, 199438; Lucy et al., 200439).

Based on their relationship with the plants PGPR are classified into two groups, symbiotic bacteria and freeliving rhizobacteria (Khan, 200540). On the basis of their residing sites: iPGPR (Verma et al., 201041) (i.e., symbiotic bacteria), example Rhizobia sp. and Frankia sp., which live inside the plant cells, produce nodules, and are localized inside the specialized structures; and ePGPR (i.e., free-living rhizobacteria), which live outside the plant cells and do not produce nodules, but still prompt plant growth (Gray and Smith, 200530).  Depending  on their  functional activities PGPR are categorized as (i) biofertilizers (increasing the availability of nutrients to plant); (ii) phytostimulators (plant growth promotion, generally through phytohormones); (iii) rhizoremediators (degrading organic pollutants); and (iv) biopesticides (controlling diseases, mainly by the production of antibiotics and antifungal metabolites) (Antoun and Prevost, 200542). Many literature studies also show that a single PGPR will often reveal multiple modes of action including biological control (Kloepper, 200343; Vessey, 200334; Ahmad et al., 200844). Genera of PGPR include Arthrobacter, Azotobacter, Azospirillum, Pseudomonas, Acetobacter, Micrococcus, Burkholderia, Bacillus, Paenibacillus, Agrobacterium, Caulobacter, Chromobacterium, Erwinia, Azospirillum, Flavobacterium, Serratia, Rhizobium and some are members of the Enterobacteriaceae (Niranjan Raj et al., 200545; Bhattacharyya and Jha, 201246).

Commercialization
A number of PGPR bacterial strains are commercially available in the form of formulated products which is used as biofertilizers and biocontrol agents. For the more extensive commercialization of plant growth promoting bacterial (PGPB) strains, a number of aspects need to be determined which include (i) determination of the traits with appropriate biological activities; (ii) consistency among regulatory agencies in different countries regarding what strains can be released to the environment, and under what conditions genetically engineered strains are suitable for environmental use; (iii) a better understanding of the advantages and disadvantages of using rhizospheric versus endophytic bacteria; (iv) selection of PGPB strains that function optimally under specific environmental conditions  (Fravel, 200747; Arora et al., 201048; Glick, 201249; Gupta et al., 201550). Moreover, commercial success of PGPR strains requires cost-effective and viable market demand, constant and broad spectrum action, safety and stability, longer shelf life, low investment and easy availability of career materials. Inorder to retain the confidence of farmers on the efficacy of the antagonistic strain quality control is vital (Bhattacharyya and Jha, 201246). According to Nandakumar et al. (200151) different stages in the process of commercialization include isolation of antagonist strains, screening, pot tests and field efficacy, mass production and formulation development, fermentation methods, formulation viability, toxicology, industrial linkages and quality control. The selection of best antagonistic strain is carried out by screening the biocontrol ability of rhizosphere bacteria for antagonism against Sclerotium rolfsii, the causal organism of root or collar rot in sunflower. The antagonists were tested for suppression of S. rolfsii rot of sunflower in greenhouse as seed and soil treatment (Rangeshwaran and Prasad, 200052).  Potential antagonists Trichoderma harzianum and Pseudomonas spp. are tested for their efficacy in field trials against Sclerotium rolfsii rot in tomato. Consortium of these bio-agents resulted in plant growth promotion, yield and simultaneously reduce the disease severity (Singh et al., 201353).  Due to variations in environmental factors a good biocontrol agent under in vitro conditions not succeeds in in vivo conditions. Similarly, the method of application also influences the success of field trials. Repeated laboratory works followed by field experiments are needed to establish excellent biocontrol agents into commercial products particularly against plant fungal pathogens (Suprapta, 201254). Thus, isolation of an effective strain is a prime criterion for better agricultural development. The first commercial product of Bacillus subtilis was developed during 1985 in United States (U.S.). 60–75% of cotton, peanut, soya bean, corn, vegetables and small grain crops raised in U.S. are now treated with commercial product of B. subtilis, which become effective against soil borne pathogens such as Fusarium and Rhizoctonia (Nakkeeran et al., 200555).

Other commercialized plant growth promoting bacterial strains include Agrobacterium radiobacter, Azospirillum brasilense, Azospirillum lipoferum, Azotobacter chroococcum, Bacillus fimus, Bacillus licheniformis, Bacillus megaterium, Bacillus mucilaginous, Bacillus pumilus, Bacillus spp., Bacillus subtilis, Bacillus subtilis var. amyloliquefaciens, Burkholderia cepacia, Delfitia acidovorans, Paenobacillus macerans, Pantoea agglomerans, Pseudomonas aureofaciens, Pseudomonas chlororaphis, Pseudomonas fluorescens, Pseudomonas solanacearum, Pseudomonas spp., Pseudomonas syringae, Serratia entomophilia, Streptomyces griseoviridis, Streptomyces spp., Streptomyces lydicus and various Rhizobia spp. (Figueiredo et al., 201056; Glick, 201249). PGPR-based commercialization is at a boom and several industries are commercializing bacterial and fungal strains as PGPR-based biofertilizers, of which some of the important PGPR strains along with their commercial products are portrayed here. The U.S. market based on the information of the committee of biological products from the American Phytopatology Society (APS) in 2005 has registered the following products: ten products based on the Bacillus (BioYield, Companion, EcoGuard, HiStick N/T, Kodiak , Mepplus, Serenade, Sonata, Subtilex, Yield- Shield), two products with Burkholderia cepacia (Deny and Intercept), and five  products based on Pseudomonas (AtEze, Bio-save, BlightBan, Frostban, Spot-Less) (Figueiredo et al., 201056). Bio-formulation of Fusarium oxysporum is commercialized by Biofox which is effective against Fusarium moniliforme. Bacterial bioformulation of Pseudomonas aureofaciens commercialized by Ecosoil is effective against Dollar spot, Anthracnose, Pythium aphanidermatum, and Michrochium patch (pink snow mold). Streptomyces griseoviridis strain K61 has been commercially formulated by AgBio which is known to inhibit Fusarium spp., Alternaria brassicola, Phomopsis spp., Botrytis spp., Pythium spp., and Phytophthora spp. that cause seed, root, stem rot, and wilt disease of ornamental and vegetable crops. A biofertilizer containing spores of Bacillus licheniformis SB3086 produced by Novozymes can act as phosphate solubilizer strain and is also effective against Dollar spot disease of plants. Commercial bioformulation of Coniothyrium minitans produced by BIOVED, Ltd., Hungary, is effective in suppressing Sclerotinia sclerotiorum and Sclerotinia minor which are phytopathogens infecting cucumber, lettuce, capsicum, tomato, and ornamental flowers. Commercial biocontrol “EcoGuard,” marketed as a concentrated suspension of spores of Bacillus licheniformis SB3086 has been found effective as a natural inhibitor of a variety of agronomically important fungal diseases – particularly dollar spot and anthracnose (Goswami et al., 201637). In India, more than 40 stakeholders from different provinces have registered themselves for the mass production of PGPRs with Central Insecticide Board (CSI), Faridabad, Haryana through collaboration with Tamil Nadu Agricultural University, Coimbatore, India (Bhattacharya and Jha, 201246). Since crops are grown under a diversity of climatic and environmental conditions causes disparity in the potentiality of PGPR based Biofertilizers (Kamilova et al., 201557). However, with better shelf life and possessing efficient strains it is possible to develop better biofertilizers exploiting PGPR in sustainable agriculture, for enhancing productivity (Glick, 201458).

Mechanisms of PGPR
The mechanisms by which bacteria can influence plant growth differ among species and strains, PGPR affect plant growth in two different ways, indirectly or directly (Castro et al., 200959).There are two mechanisms for promoting plant growth. The direct promotions of plant growth by PGPR involve either providing the plant with resources they lack. This facilitates higher plant yield. Biological means of providing the nutrients such as nitrogen and phosphorus are ideal than chemical sources which are expensive and cause environmental hazards or through compound’s that are synthesized by the bacterium, for example phytohormones (Lucy et al., 200440; Khalid et al., 200460; Glick, 201249). Indirectly, the bacteria may exert a positive influence on plant growth by lessening certain deleterious effects of a pathogenic organism by producing antagonistic substances.

Direct Mechanisms
The direct mechanisms observed in PGPR include N2-fixation, mobilization of nutrients via production of phosphatases, siderophores, or organic acids, and production of phytohormones and enzymes.

Nitrogen Fixation
Nitrogen being a primary limiting factor in agriculture found deficient due to various environmental factors. 65% of the nitrogen currently utilized in agriculture is obtained through biological nitrogen fixation, also important to sustain   crop production systems in future (Dakora, 200361). PGPR strains play a major role in nitrogen fixation and make it assimilable form for plants. Nitrogenase (nif) genes required for nitrogen fixation in nitrogen fixing bacteria are more complex. So for improving this process genetic strategies have been utilized to modify the genes (Glick, 201249; Souza et al., 201562). PGPR follow two mechanism of nitrogen fixation. In symbiotic nitrogen fixation, legume crops undergo biological nitrogen fixation through symbiotic association with bacteria and meet their own needs without depending external sources (Bhattacharyya and Jha, 201246; Gopalakrishnan et al., 20153). Symbiotic bacteria which act as PGPR are Rhizobium, Bradyrhizobium, Sinorhizobium, and Mesorhizobium with leguminous plants, Frankia with non-leguminous trees and shrubs (Zahra, 200163). Free living nitrogen fixers, which are non symbiotic types survive close to root without penetration, fixed nitrogen that are acquired  through uptake contribute to the nitrogen account of the plants (Goswami et al., 201637). Non-symbiotic nitrogen fixing rhizospheric bacteria belongs to genera including Azoarcus, Azotobacter, Acetobacter, Azospirillum, Burkholderia, Diazotrophicus, Enterobacter, Gluconacetobacter, Pseudomonas and Cyanobacteria, Anabaena, Nostoc (Vessey, 200334).

Many species of microorganisms are used in the cultivation of plants of economic interest, facilitating the host plant growth without the use of nitrogenous fertilizers. For instance, the production of soybean (Glycine max L.)  is an excellent example of the efficiency of biological nitrogen fixation through the use of different strains of Bradyrhizobium sp., such as B. japonicum and B. elkanii (Alves et al., 200464; Torres et al., 201265). The importance of endophytic nitrogen fixing bacteria has also been the object of studies in non leguminous plants such as sugarcane (Saccharum officinarum L) (Thaweenut et al., 201166). Other studies have suggested that Bradyrhizobia colonize and express nif H not only in the root nodules of leguminous plants but also in the roots of sweet potatoes (Ipomoea batatas L.), acting as diazotrophic endophytes (Terakado-Tonooka et al., 200867). The plant growth promoting bacteria related to genus Azospirillum have been largely studied because of their efficiency in promoting the growth of different plants of agronomical interest. The genus Burkholderia includes species that fix nitrogen B. vietnamiensis, a human pathogenic species, was efficient in colonizing rice roots and fixing nitrogen (Govindarajan et al., 200868). In addition to Burkholderia, the potential of biological nitrogen fixation and endophytic colonization of bacteria belonging to the genera Pantoea, Bacillus and Klebsiella were also confirmed in different maize genotypes (Ikeda et al., 201369).

Phosphate solubilisation
Next to nitrogen, phosphorus is the important key element in the nutrition of plants. It exists in both inorganic (bound, fixed, or labile) and organic (bound) forms. The availability of phosphorus to plants is influenced by pH, compaction, aeration, moisture, temperature, texture and organic matter of soils, crop residues, extent of plant root systems and root exudate secretions and available soil microbes (Gopalakrishnan et al., 20153). Phosphorus is involved in metabolic processes of plant, as photosynthesis, energy transfer, signal transduction, macromolecular biosynthesis and respiration (Khan, et al., 201070). Soil phosphorus cycle mediate phosphorus availability to plants. PGPR’s directly solubilise and mineralise inorganic phosphorus or facilitate the mobility of organic phosphorus through microbial turnover and/or increase the root system (Richardson and Simpson, 201171). These bacteria secrete different types of organic acids which lower the pH in the rhizosphere and thus release the phosphorus available to plants (Kaur et al., 201672). Bacteria from genera such as Achromobacter, Agrobacterium, Bacillus, Enterobacter, Erwinia, Escherichia, Flavobacterium, Mycobacterium, Pseudomonas and Serratia are highly efficient in solubilising unavailable complexed phosphate into available inorganic phosphate ion (Goldstein, 200173). Rhizobia, including R. leguminosarum, R. meliloti, M. mediterraneum, Bradyrhizobium sp. and B. japonicum are the potential phosphate solubilizers (Vessey, 200334; Egamberdiyeva et al., 200474; Rodrigues et al., 200675).

Siderophore
The transition metal iron is an essential micronutrient and bioactive metal crucial for the growth and metabolism of bacteria. Iron plays a key role in electron transport, oxidation–reduction reactions, detoxification of oxygen radicals, synthesis of DNA precursors and in many other biochemical processes (Hider and Kong, 201076). Based on their iron-coordinating functional groups, structural features and types of ligands, bacterial siderophores have been classified into four main classes such as carboxylates, hydroxamates, phenol catecholates and pyoverdines (Mohandas, 200477; Fernandez et al., 200578). Generally, rhizobacteria differs regarding the siderophore cross-utilizing ability. Some are capable of using siderophores of the same genus (homologous siderophores) while others could utilize those produced by other rhizobacteria of different genera (heterologous siderophores) (Khan et al., 200979).

In aerobic environments, iron occurs in the form of insoluble hydroxides and oxyhydroxides are not accessible to both plants and microbes (Rajkumar et al., 201080). Being a transition element, iron gets rapidly oxidized from soluble ferrous (Fe2) to insoluble ferric (Fe3) state (Murugappan et al., 201281). Siderophores enhances the iron bioavailability by influencing the low solubility of iron (Wittenwiler, 200782). Siderophores attach on the mineral surface and facilitate dissolution by coordinating the iron atom in a soluble complex (Kraemer et al., 200683). Under iron limiting conditions microorganisms and plants rely on chelating agents to solubilise and transport inorganic iron. The membrane receptor and the ferric siderophore transporter are the common transporter for high affinity microbial acquisition of iron (Neilands, 198184; Crowley et al., 199185). Microbes release siderophores to scavenge iron from these mineral phases by formation of soluble Fe3+ complexes that can be taken up by active transport mechanisms (Saharan and Nehra, 201186). Bacteria secrete the siderophore to overcome the iron limitation and provide plants with Fe, enhancing their growth directly by increasing the availability of iron in the soil surrounding the roots (Krewulak and Vogel, 200887; Vejan et al., 201688). Plants uptake iron when they are able to recognize the bacterial ferric-siderophore complex (Masalha et al., 200089). Not only iron, siderophores also form stable complexes with other heavy metals that are of environmental concern, such as  cadmium, copper, lead and zinc, as well as with radionuclide’s including uranium (Neubauer et al., 200090). Binding of the siderophore to a metal increases the soluble metal concentration (Rajkumar et al., 201080). Hence, bacterial siderophores help to alleviate the stresses imposed on plants by high soil levels of heavy metals.

Microorganisms have evolved highly specific pathways that employ low molecular weight, high affinity iron chelators to solubilise iron prior to transport. Gram-negative bacteria take up ferri-siderophore complexes via specific outer membrane receptors in a process that is driven by the cytosolic membrane potential and mediated by the energy-transducing TonB-ExbB-ExbD system. Bacteria, such as Gram-positive, that lack an outer membrane, use binding-protein-dependent ABC permeases to allow ferri-siderophores to traverse their cytosolic membrane (Crowely et al., 199185; Andrews et al., 200391).

Phytohormones
Chemicals occurring naturally within plant tissues have a regulatory, rather than a nutritional role in growth and development. These compounds, which are generally active at very low concentrations, are known as phytohormones or plant growth substances (George et al., 200892). Classes of well-known phytohormones include auxins, gibberellins, cytokinins, ethylene, and abscisic acid and soil micro-organisms, particularly the rhizosphere bacteria, possess the potential to produce these hormones (Zakir et al., 200424).

Indole-3-acetic acid
Indole-3-acetic acid (IAA) is the member of the group of phytohormones and is generally considered the most important native auxin which is low-molecular weight, organic substances. This substance termed auxin was identified as indole-3-acetic acid (Kögl and Kostermans, 193493; Went and Thimann, 193794). This phytohormone auxin is a key regulator of many aspects of plant growth and development, including cell division and elongation, differentiation, tropisms, apical dominance, senescence, abscission, and flowering (Woodward and Bartel, 200595 ; Teale et al., 200696 ; Ahemad and Kibret, 201497). The auxin level is usually higher in the rhizosphere, where high percentage of rhizosphere bacteria is likely to synthesize auxin as secondary metabolites because of the rich supplies of root exudates. The production of auxin (IAA), has been recognized as an important factor in direct plant-growth-promoting abilities of rhizosphere bacteria (Dilfuza, 201198).  For various PGPR, it has been demonstrated that enhanced root proliferation is related to bacterial IAA biosynthesis. Upon inoculation of plants with PGPR, a change in root architecture is observed, mainly as an increase in root hairs and lateral roots and shortening of the root length. Also, rhizobacterial IAA loosens plant cell walls and as a result facilitates an increasing amount of root exudation that provides additional nutrients to support the growth of rhizosphere bacteria (Glick, 201249). Moreover, down-regulation of IAA as signalling is associated with the plant defense mechanisms against a number of phyto-pathogenic bacteria as evidenced in enhanced susceptibility of plants to the bacterial pathogen by exogenous application of IAA or IAA produced by the pathogen (Spaepen and Vanderleyden, 201199).

IAA biosynthesis is widespread among plant-associated bacteria (Patten and Glick, 1996100; Giickmann et al., 1998101).  Bacteria can use this phytohormone to interact with plants as part of their colonization strategy, including phytostimulation and basal plant defense mechanisms. IAA can also be a signaling molecule in bacteria and therefore can have a direct effect on bacterial physiology (Spaepen et al., 2007102). More than 80% of the bacteria isolated from the rhizosphere are capable to synthesize IAA (Khalid et al., 200460). IAA production under in vitro condition has been reported by many researches, in Azospirillum sp. (Lambrecht et al., 2000103; Dobbelaere et al., 2001104), Azotobacter sp. (Zahir et al., 2000105), Azotobacter chrococcum, Bacillus megaterium BHUPSB14, Pseudomonas fluorescens, P.putida (Patten and Glick, 2002106; Verma et al., 201041; Peyvandi et al., 2010107), Rhizobium sp. (Ghosh et al., 2008108),  Pseudomonas aeruginosa (Khare and Arora, 2010109), Acetobacter diazotrophicus L1(Patil et al., 2011110) and in Rhizobium leguminosarum  (Dazzo et al., 2000111). Tsavkelova et al. (2006112) observed IAA production in fungi in genera Aspergillus sp., Fusarium sp. and Paecilomyces sp. Ruanpanun et al. (2010113) found high IAA producing nematophagous actinomycete and fungal isolates such as Streptomyces sp. and in Aspergillus sp.

Bacterial production of IAA suggests that the pathways involved in IAA production may play an important role in defining the effect of the bacterium on the plant. Though bacterial biosynthesis of IAA can occur by a variety of pathways, tryptophan has been identified as a main precursor for IAA biosynthesis pathways in bacteria (Sarwar and Kremer, 1995114; Patten and Glick, 1996100; Kravchenko et al., 2004115; Kamilova et al. 2006116). According to Ghosh and Basu (2006117) among the three different isomers of tryptophan, the bacteria produced higher amount of IAA with the supplementation of L-tryptophan (138 µg/ml) than in D-tryptophan (15 µg/ml) or DL-tryptophan (84 µg/ml). In earlier work Dullaart (1970118) explained this process due to the utilisation of this essential amino acid partly in protein synthesis and partly for the formation of other indole compounds in addition to IAA. The indole-3-acetamide (IAM) pathway is the best characterized pathway in bacteria. In this two-step pathway tryptophan is first converted to IAM by the enzyme tryptophan-2-monooxygenase (IaaM), encoded by the iaaM gene. In the second step IAM is converted to IAA by an IAM hydrolase (IaaH), encoded by iaaH. In plant-associated bacteria, both the IAM and the indole-3- pyruvic acid (IPyA) pathway are distributed among the sequenced genomes. Phytopathogenic organisms tend to use the IAM pathway to produce IAA, whereas beneficial bacteria tend to use the IPyA pathway (Spaepen et al., 2007102; Mano and Nemoto, 2012119). This helps the bacteria to evade the plant regulatory signals and so the IAA induces uncontrolled growth in plant tissues. In contrast the useful bacteria such as PGPR synthesize IAA via the indole pyruvic acid pathway and the IAA secreted is thought to be strictly regulated by the plant regulatory signals (Patten and Glick, 1996100).

Cytokinins
Cytokinins are a class of phytohormones which are known to promote cell divisions, cell enlargement and tissue expansion in certain plant parts (Werner et al., 2003120). Cytokinins play a major or minor role throughout development, from seed germination to leaf and plant senescence and modulate physiological processes important throughout the life of the plant, including photosynthesis and respiration (Salisbury and Ross, 1992121; Arshad and Frankenberger, 1993122). Plants and plant associated microorganisms have been found to contain over 30 growth promoting compounds of the cytokinin group. It has been found that as many as 90% of microorganisms found in the rhizosphere are capable of releasing cytokinins (Nieto and Frankenberger, 1990123). Several plant growth promoting rhizobacteria  Azotobacter sp., Rhizobium sp., Pantoea agglomerans, Rhodospirillum rubrum, Pseudomonas fluorescens, Bacillus subtilis and Paenibacillus polymyxa can produce cytokinins along with other growth-promoting substances (Gutiérrez-Mañero et al., 2001124). Cytokinin production has been reported in various PGPR, like Arthrobacter giacomelloi, Azospirillum brasilense, Bradyrhizobium japonicum, Bacillus licheniformis, P. fluorescens and Paenibacillus polymyxa (Timmusk et al., 1999125; Per-rig et al., 2007126).  Plant responses to exogenous applications of cytokinin result in either one of the following effects (a) enhanced cell division; (b) enhanced root development; (c) enhanced root hair formation; (d) inhibition of root elongation; (e) shoot initiation and certain other physiological responses (Frankenberger and Arshad, 1995127).

Gibberellins
Gibberellins are a class of phytohormones most commonly associated with modifying plant morphology by the extension of plant tissue, particularly stem tissue (Salisbury, 1994128). These are synthesized by higher plants, fungi, and bacteria. They are involved in several plant developmental processes, including cell division and elongation, seed germination, stem elongation, flowering, fruit setting, and delay of senescence in many organs of a range of plant species (MacMillan, 2002129). They can also regulate root hair abundance and hence promotes the root growth (Bottini et al., 2004130). The ability of bacteria to synthesize gibberellins-like substances was first described in Azospirillum brasilense (Tien et al., 1979131) and Rhizobium (Williams and Mallorca, 1982132). Production of gibberellins had been detected in different bacterial genera that inhabit the plant root system including  Azotobacter, Arthrobacter, Azospirillum, Pseudomonas, Bacillus., Acinetobacter, Flavobacterium, Micrococcus, Agrobacterium, Clostridium, Rhizobium, Burkholderia and Xanthomonas (Joo et al., 2005133; Tsakelova et al., 2006112; Hayat et al., 20106). Plant growth promotion by gibberellin-producing plant growth promoting bacteria and this positive effect on plant biomass is frequently associated with an increased content of gibberellins in plant tissues was reported by several workers (Joo et al., 2005133; Kang et al., 201016).

Abscisic acid
Abscisic acid (ABA) plays a primary role in water-stressed environment, such as found in arid and semiarid climates where it helps in combating the stress through stomatal closure of leaves. Therefore, its uptake by and transport in plant and its presence in the rhizosphere could be extremely important for plant growth under water stress conditions (Frankenberger and Arshad, 1995127). Rhizobium sp., B. japonicum and Azospirillium sp. had been reported to produce abscisic acid (Dangar and Basu, 1987134; Dobbelaere et al., 2003135; Boiero et al., 2007136).

Ethylene
Apart from being a plant growth regulator, ethylene has also been recognized as a stress hormone (Saleem et al., 2007137). Ethylene is essential for the growth and development of plants, but it has different effects on plant growth depending on its concentration in root tissues. At high concentrations, it can be harmful, as it induces defoliation and cellular processes that lead to inhibition of stem and root growth as well as premature senescence, all of which lead to reduced crop performance (Li et al., 2005138; Bhattacharyya and Jha, 201246). Under stress conditions like those  generated by salinity, drought, water logging, heavy metals and pathogenicity, the  endogenous level of ethylene is significantly increased which negatively affects the overall plant growth. Plant growth promoting rhizobacteria which possess the enzyme, 1-aminocyclopropane-1-carboxylate (ACC) deaminase, which is the precursor for ethylene (Chen et al., 2013139) is secreted into the rhizosphere and is  readsorbed by the roots, where it is converted into ethylene. This accumulation of ethylene leads to a downward spiral effect, as poor root growth leads to a diminished ability to acquire water and nutrients, which, in turn, leads to further stress (Martinez-Viveros et al., 2010140). The destruction of ethylene is done by PGPR via the enzyme ACC deaminase. This enzyme can diminish or prevent some of the harmful effects of the high ethylene levels (Glick et al., 1998141). The ACC deaminase acts on ACC, an immediate ethylene precursor in higher plants, degrading this chemical to alphaketobutyrate and ammonium, (Glick et al., 1998141; Mayak et al., 2004142). Rhizosphere bacteria with ACC deaminase activity belonging to the genera, Achromobacter (Govindasamy et al., 2008143), Azospirillum (Li et al., 2005138), Bacillus (Ghosh et al., 2003144), Enterobacter (Li and Glick, 2001145), Pseudomonas (Govindasamy et al., 2008143) and Rhizobium (Duan et al., 2009146) have been isolated from different soils.

Indirect Mechanisms
There are many indirect ways through which PGPR act as plant growth promoters with their biocontrol properties and induction of systemic resistance against phytopathogens. Plant growth promoting organisms have certain properties for biocontrol of various phytopathogens. This includes (1) production of antibiotics; (2) secretion of siderophores enabling iron uptake depriving the fungal pathogens in the vicinity; (3) production of lytic enzymes such as chitinase, β-1, 3 glucanase, protease and lipase which lyse the pathogenic fungal and bacterial cell walls; (4) induces systemic resistance in plants by metabolites (Zahir et al., 200424; Hafeez et al., 2006147; Narayanasamy, 2008148; Reddy, 2013149).

Antibiotics
One of the most effective mechanism by which PGPR employ to prevent proliferation of phytopathogens is the synthesis of antibiotics. Antibiotics include a heterogeneous group of organic, low-molecular-weight compounds that are deleterious to the growth or metabolic activities of other microorganisms (Duffy, 2003150). There are six classes of antibiotic compounds linked to the biocontrol of root diseases are, phenazines, phloroglucinols, pyoluteorin, pyrrolnitrin, cyclic lipopeptides (all of which are diffusible) and hydrogen cyanide (HCN which is volatile) (Haas and Défago, 200518). The mechanism of action is to inhibit synthesis of pathogen cell walls, influence membrane structures of cells and inhibit the formation of initiation complexes on the small subunit of the ribosome (Maksimov et al., 2011151). An efficient antibiotic, 2, 4-diacetylphloroglucinol (DAPG) produced by pseudomonads, causes membrane damage to Pythium spp. and is particularly inhibitory to zoospores of this oomycete (de Souza et al., 2003152).

Lytic enzymes
The growth and activities of pathogens can be suppressed by the secretion of lytic enzymes. These are cell wall degrading enzymes such as glucanases, proteases, chitinases, and lipases etc, secreted by biocontrol strains of PGPR involved in the lysis of fungal cell wall (Neeraja et al., 2010153).These enzymes either digest the enzymes or deform components of cell wall of fungal pathogens. Hydrolytic enzymes directly contribute in the parasitisation of phytopathogens and rescue plant from biotic stresses. The role of three types of chitinolytic enzymes are as follows (a) 1, 4-β-ILT-acetylglucosaminidases splits the chitin polymer into GlcNAc monomers in an exo-type fashion; (b) endochitinases cleave randomly at internal sites over the entire length of the chitin microfibril; and (c) exochitinases catalyse the progressive release of diacetylchitobiose in a stepwise fashion such that no monosaccharide’s or oligosaccharides are formed (Haran et al., 1996154). β -Glucanases can act via two possible mechanisms, Exo-β-glucanases hydrolyse the β-glucan chain by sequentially cleaving glucose residues from the non-reducing end. Endo- β -glucanases cleave β -linkages at random sites along the polysaccharide chain, releasing smaller oligosaccharides (Pitson et al., 1993155).

Induced systemic resistance
The uses of plant growth promoting strains are reported to trigger the resistance of plants against pathogens (Ramamoorthy et al., 2001156). Induced resistance (ISR) is a state of enhanced defensive capacity developed by a plant when appropriately stimulated. Systemic acquired resistance (SAR) and induced systemic resistance (ISR) are two forms of induced resistance which can be differentiated on the basis of the nature of the elicitor and the regulatory pathways involved (Choudhary et al., 2007157). SAR can be triggered by exposing the plant to virulent, avirulent, and non pathogenic microbes and involves accumulation of pathogenesis-related proteins (chitinase and glucanase), and salicylic acid. ISR does not involve the accumulation of pathogenesis-related proteins or salicylic acid, but instead, relies on pathways regulated by jasmonate and ethylene and these hormones stimulate the host plant’s defense responses against a variety of plant pathogens (Yan et al., 2002158; Glick, 201249). Bacterial components too induce induced systemic resistance such as lipopolysaccharides, flagella, siderophores, etc., (Doombos et al., 2012159). PGPR-mediated induced systemic resistance has been shown to effectively suppress Phytophthora blight caused by Phytophthora capsici on squash (Zhang et al., 2010160).

CONCLUSION

Plant growth promoting rhizobacteria in rhizosphere soil is highly dynamic, more versatile in transforming, mobilizing and solubilising the nutrients. Therefore, the rhizobacteria are the dominant deriving forces in recycling the soil nutrients and consequently, they are crucial for soil fertility. They may be extensively used in plant growth promotion as it acts  as a plant nourishment and enrichment source  which  would replenish  the nutrient cycle between the soil and  plant roots , exhibits detoxifying potential, controls phytopathogen thereby exerts a positive influence on crop productivity and ecosystem functioning, hence can  be  implemented  in agriculture. With better research and development, these microbial populations use would become a reality and instrumental and build stability and productivity of agro-ecosystems, thus leading us towards an ideal agricultural system with sustainability, improvement in human health, benefits environment and ecosystem and leads to the production of adequate food for the increasing world population.

REFERENCES

  1. Zeder, M. A. Evolutionary biology and the emergence of agriculture: the value of co-opted models of evolution in the study of culture change. In: Macroevolution in human prehistory: Evolutionary theory and Processual Archaeology. New York: Springer, 2009; pp 157-210.
  2. Bishnoi, U. PGPR Interaction: An Ecofriendly Approach Promoting the Sustainable Agriculture System. Bot.Res., 2015; 75: 81-113.
  3. Gopalakrishnan, S., Sathya, A., Vijayabharathi, R., Varshney, R.K., Laxmipathi Gowda, C.L., Krishnamurthy, L. Plant growth promoting rhizobia: challenges and opportunities. , 2015; 5: 355–377.
  4. Shenoy, V.V., Kalagudi, G.M., Gurudatta, B.V. Towards nitrogen autotrophic rice. Sci., 2001; 81:451-457.
  5. Adesemoye, A.O., Kloepper, J.W. Plant– microbes interactions in enhanced fertilizer-use efficiency. Microbiol.Biotechnol., 2009; 85: 1–12.
  6. Hayat, R., Ali, S., Amara, U. Soil beneficial bacteria and their role in plant growth promotion: A review. Microbiol., 2010; 60:579–598.
  7. Burd, G.I, Dixon, D.G., Glick, B.R. Plant growth promoting bacteria that decrease heavy metal toxicity in plants. Can J Microbiol., 2000; 46 (3): 237–245.
  8. Zhuang, X., Chen, J., Shim, H., Bai, Z. New advances in plant growth promoting rhizobacteria for bioremediation. Environ Int., 2007; 33 (3): 406–413.
  9. Zaidi, S., Usmani, S., Singh, B.R., Musarrat, J. Significance of Bacillus subtilis strains SJ-101 as a bioinoculant for concurrent plant growth promotion and nickel accumulation in Brassica juncea. Chemosphere., 2008; 64:991–997.
  10. Gouda, S., Kerry, R.G., Das, G., Paramithiotis, S., Shine, H.S., Patra, J.K. Revitalization of plant growth promoting rhizobacteria for sustainable development in agriculture. Res., 2018; 206:131–140.
  11. Hiltner, L. About recent experiences and problems in the field of soil bacteriology with special Consideration of green manure and fallow. Dtsch. Land. Gesel., 1904; 98:59–78.
  12. Khalid, A., Akhtar, M.J., Mahmood, M.H., Arshad, M. Effect of substrate-dependent microbial ethylene production on plant growth. Microbiology., 2006; 75: 231-236.
  13. Jha, C. K., Patel, D., Rajendran, N., Saraf, M. Combinatorial assessment on dominance and informative diversity of PGPR from rhizosphere of Jatropha curcas J. Basic Microbiol., 2010 ; 50: 211–217.
  14. Govindasamy, V., Senthilkumar, M., Magheshwaran, V., Kumar, U., Bose, P., Sharma, V., Annapurna, K. Bacillus and Paenibacillus : Potential PGPR for sustainable agriculture. In: Plant growth and health promoting bacteria (Maheshwari, DK, ed.). Berlin: Springer-Verlag, 2011; pp 333–364.
  15. Dakora, F.D., Philips, D.A. Root exudates as mediators of mineral acquisition in low-nutrient environments. Plant Soil., 2002; 245: 35–47.
  16. Kang, B.G., Kim, W.T., Yun, H.S., Chang, S.C. Use of plant growth-promoting rhizobacteria to control stress responses of plant roots. Plant Biotechnol Rep., 2010; 4: 179-183.
  17. Nardi, , Concheri, G., Pizzeghello, D., Sturaro, A., Rella, R., Parvoli, G. Soil organic matter mobilization by root exudates. Chemosphere., 2000; 5: 653–65.
  18. Haas, D., Défago, G. Biological control of soil-borne pathogens by Fluorescent Pseudomonads. Rev. Microbiol., 2005; 10: 1-13.
  19. Badri, D.V., Weir, T. L., Van der Lelie, D., Vivanco, J. M. Rhizosphere chemical dialogues: plant-microbe interactions. Curr Opin Biotechnol., 2009 ; 20: 642-650.
  20. Dennis, P.G., Miller, A.J., Hirsch, P.R. Are root exudates more important than other sources of rhizodeposits in structuring rhizosphere bacterial communities?Fems Microbiol Ecol., 2010; 72 (3): 313–327.
  21. Doornbos, R.F., Van Loon, L.C., Peter, A.H.M., Bakker, A. Impact of root exudates and plant defense signaling on bacterial communities in the rhizosphere. Sustain. Dev., 2012; 32: 227-243.
  22. Chaparro, J.M., Sheflin, A.M., Manter, D.K., Vivanco, J.M. Manipulating the soil microbiome to increase soil health and plant fertility. Fertil. soil., 2012; 48 (5):489-499.
  23. Barea, J.M., Pozo, M.J., Azcon, R., Aguilar, C.A. Microbial cooperation in the rhizosphere. Exp. Bot., 2005; 56 (417):1761–1778.
  24. Zahir, A.Z., Arshad, M., Frankenberger, W.T. Jr. Plant growth promoting rhizobacteria: application and perspectives in Agriculture. Adv Agron., 2004; 81:97–168.
  25. Glick, B.R., Cheng, Z., Czarny, J., Duan, J. Promotion of plant growth by ACC deaminase-producing soil bacteria.  J. Plant Pathol., 2007; 119 (3):329–339.
  26. Lagos, M.L., Maruyama, F., Nannipieri, P., Mora, M.L., Ogram, A., Jorquera, M.A. Current overview on the study of bacteria in the rhizosphere by modern molecular techniques: a mini‒review. Soil Sci. Plant Nutr., 2015; 15 (2): 504-523.
  27. Kloepper, J.W., Zablotowick, R.M., Tipping, E.M., Lifshitz, R. Plant growth promotion mediated by bacterial rhizosphere colonizers. In: The Rhizosphere and Plant Growth (Keister, DL, Cregan, PB, ed.). Dordrecht, Netherlands: Kluwer Academic Publishers, 1991; pp 315-326.
  28. Uren, N.C. Types, amounts, and possible functions of compounds released into the rhizosphere by soil-grown plants. In: The rhizosphere: biochemistry and organic substances at the soil–plant interface (Pinton, R, Varanini, Z, Nannipieri, P, ed.). Boca Rato´n: CRC Press, 2007; pp 1–22.
  29. J., Jaramillo-López, P., Nájera-Rincon, M., Gonzaléz-Esquivel, C.E. Journal of Soil Science and Plant Nutrition, Biotic interactions in the rhizosphere in relation to plant and soil nutrient dynamics. J. Soil Sci. Plant Nutr, 2015; 15 (2): 449-463.
  30. Gray, E.J., Smith, D.L. Intracellular and extracellular PGPR: commonalities and distinctions in the plant-bacterium signalling processes. Soil Biol. Biochem. 2005; 37: 395–412.
  31. Das, A.J., Kumar, M., Kumar, R., Plant Growth Promoting Rhizobacteria (PGPR): An Alternative of Chemical Fertilizer for Sustainable, Environment Friendly Agriculture. J. Agriculture & Forestry Sci., 2013; 1(4): 21-23.
  32. Whipps, J.M., Microbial interactions and biocontrol in the rhizosphere. Exp.Bot., 2001; 52 (1): 487-511.
  33. Kloepper, J.W., Schroth, M.N. Relationship of in vitro antibiosis of plant growth promoting rhizobacteria to plant growth and the displacement of root microflora. , 1981; 71:1020–1024.
  34. Vessey, K.J. Plant growth promoting rhizobacteria as biofertilizers. Plant Soil., 2003; 255 (2): 571–586.
  35. Khalid, A., Arshad, M., Shaharoona, B., Mahmood, T. Plant growth promoting rhizobacteria and sustainable agriculture. In: Microbial Strategies for Crop Improvement (Khan, MS, ed.). Verlag Berlin Heidelberg: Springer, 2009; pp133-160.
  36. llangumuran, G.,Smith, D.L. Plant Growth Promoting Rhizobacteria in Amelioration of Salinity Stress: A Systems Biology Perspective. Plant Sci., 2017; 8:1-14.
  37. Goswami, D., Thakker.J.N, Dhandhukia, P.C. Portraying mechanics of plant growth promoting rhizobacteria (PGPR): A review. Cogent Food Agric., 2016; 2:1-19.
  38. Kloepper, J.W. Plant growth-promoting rhizobacteria (other systems) In: Azospirillum/ Plant Associations (Okon, Y, ed.). Boca Raton, FL, USA: CRC Press, 1994; pp 111-118.
  39. Lucy M., Reed, E., Glick, B.R. Applications of free living plant growth promoting rhizobacteria. Antonie Van Leeuwenhoek., 2004; 86 (1): 1–25.
  40. Khan, A.G. Role of soil microbes in the rhizosphere of plants growing on trace metal contaminated soils in phytoremediation. J Trace Elem Med Biol., 2005; 18 (4):  355-364.
  41. Verma, J.P., Yadav, J., Tiwari, K.V., Lavakush, Singh, V. Impact of plant growth promoting rhizobacteria on crop production. J. Agric.Res., 2010; 5 (11): 954-983.
  42. Antoun, H., Prévost, D. Ecology of plant growth promoting rhizobacteria. In: PGPR: biocontrol and biofertilization (Siddiqui, ZA, ed.). Dordrecht: Springer, 2005; pp 1–38.
  43. Kloepper, J., 2003. A review of mechanisms for plant growth promotion by PGPR In: 6th International PGPR Workshop (Reddy, MS, Anandaraj, M, Eapen, SJ, Sarma, YR, Kloepper, JW, ed.). Calicut, India: Indian Institute of Spices Research, 2003; pp 81–92.
  44. Ahmad, F., Ahmad, I., Khan, M.S. Screening of free-living rhizospheric bacteria for their multiple plant growth promoting activities. Res., 2008; 163: 173-181.
  45. Niranjan Raj, S., Shetty, H.S., Reddy, M.S. Plant growth-promoting Rhizobacteria: potential green alternative for plant productivity. In: PGPR: Biocontrol and Biofertilization (Siddiqui, ZA, ed.). Dordrecht, Netherlands. Springer, 2005; pp 197-216.
  46. Bhattacharyya, P.N., Jha, D. K. Plant growth-promoting rhizobacteria (PGPR): emergence in agriculture. J. Microbiol.Biotechnol., 2012; 28 (4): 1327–1350.
  47. Fravel, D. Commercialization of biocontrol agents for use against plant pathogens. In: IX Reunia˜o Brasileira sobre Controle Biolo´gico de Doenc¸as de Plantas, Campinas, (Paulo, S, ed.). Brasil: CD-ROM, 2007; pp 1–2.
  48. Arora, N.K.,Khare,,Maheshwari,D.K. PGPR:constraintsinbioformulation,commercializationandfuturestrategies.In:Plantgrowthandhealthpromoting bacteria (Maheshwari, DK,ed.).Dorderecht: Springer, 2010; pp 97-116.
  49. Glick, B.R. Plant Growth-Promoting Bacteria: Mechanisms and Applications. , 2012: 1-16.
  50. Gupta, G., Parihar, S.S., Ahirwar, N.K., Snehi, S.K., Singh, V. Plant Growth Promoting Rhizobacteria (PGPR): Current and Future Prospects for Development of Sustainable Agriculture. J Microbiol Biochem Technol., 2015; 7(2): 096-102.
  51. Nandakumar, R., Babu, S., Viswanathan, R., Sheela, J., Raguchander, T., Samiyappan, R. A new bio-formulation containing plant growth promoting rhizobacterial mixture for the management of sheath blight and enhanced grain yield in rice. Biocontrol., 2001; 46 (4):493–510.
  52. Rangeshwaran, R., Prasad, R.D. Biological control of Sclerotium rot of sunflower. Indian Phytopathol., 2000; 53 (4): 444-449.
  53. Singh, S.P., Singh, H.B., Singh, D.K. Trichoderma Harzianum and Pseudomonas mediated management of Sclerotium rolfsii rot in tomato (Lycopersicon esculentum mill.). Bioscan., 2013; 8 (3): 801-804.
  54. Suprapta, D.N., Potential of Microbial Antagonists as biocontrol agents against plant fungal pathogens. ISSAAS., 2012; 18 (2):1-8.
  55. Nakkeeran, S., Fernando, W.G.D., Siddiqui, Z.A. Plant growth promoting rhizobacteria formulations and its scope in commercialization for the management of pests and diseases. In: PGPR: biocontrol and biofertilization (Siddiqui, ZA, ed.). Dordrecht, Netherlands: Springer, 2005; pp 257–296.
  56. Figueiredo, M.V.B., Seldin, L., de Araujo, F.F., Ramos Mariano, R.D.L. Plant Growth Promoting Rhizobacteria: Fundamentals and Applications. In: Plant Growth and Health Promoting Bacteria (Maheshwari, DK, ed.). Verlag, Berlin Heidelberg: Springer, 2010; pp 21-43.
  57. Kamilova, F., Okon, Y., de Weert, S., Hora, K. Commercialization of microbes: Manufacturing, inoculation, best practice for objective field testing, and registration. In: Principles of plant-microbe interactions (Lugtenberg, B, ed.). International: Springer 2015; pp 319–327.
  58. Glick, B.R. Bacteria with ACC deaminase can promote plant growth and help to feed the world. Microbiol Res., 2014; 169 (1): 30-39.
  59. Castro, R.O., Cornejo, H.A.C., Rodriguez, L.M., Bucio, J.L. The role of microbial signals in plant growth and development. Plant Signal Behav., 2009; 4 (8):701–712.
  60. Khalid, A., Arshad, M., Zahir, Z.A. Screening plant growth-promoting rhizobacteria for improving growth and yield of wheat. Appl. Microbiol., 2004; 96 (3): 473–480.
  61. Dakora, F.D. Defining new roles for plant and rhizobial molecules in sole and mixed plant cultures involving symbiotic legumes. New Phytol., 2003; 158: 39 – 49.
  62. Souza, R.D., Ambrosini, A., Passaglia, L.M.P. Plant growth-promoting bacteria as inoculants in agricultural soils. Mol. Biol., 2015; 38, (4): 401-419.
  63. Zahran, H.H. Rhizobia from wild legumes: diversity, taxonomy, ecology, nitrogen fixation and biotechnology. Biotechnol., 2001; 91: 143-153.
  64. Alves, B.J.R., Boddey, R.M., Urquiaga, S. The success of BNF in soybean in Brazil. Plant Soil., 2004; 252:1-9.
  65. Torres, A.R, Kaschuk, G., Saridakis, G.P., Hungria, M. Genetic variability in Bradyrhizobium japonicum strains nodulating soybean Glycine max (L.) Merrill. World J Microbiol Biotechnol., 2012; 28:1831-1835.
  66. Thaweenut, N., Hachisuka, Y., Ando, S., Yanagisawa, S., Yoneyama, T. Two seasons’ study on nif H gene expression and nitrogen fixation by diazotrophic endophytes in sugarcane (Saccharum hybrids): Expression of nifH genes similar to those of rhizobia. Plant Soil., 2011; 338:435-449.
  67. Terakado-Tonooka, J., Ohwaki, Y., Yamakawa, H., Tanaka, F., Yoneyama, T., Fujihara, S. Expresses nifH genes of endophytic bacteria detected in field-growth sweet potatoes (Ipomoea batata). Microbes Environl., 2008; 23:89-93.
  68. Govindarajan, M., Balandreau, J., Kwon, S.W., Weon, H.Y., Lakshminarasimhan, C. Effects of the inoculation of Burkholderia vietnamensis and related endophytic diazotrophic bacteria on grain yield of rice. Microb Ecol., 2008; 55:21-37.
  69. Ikeda,G, Bassani, L.L, Adamoski, D., Stringari, D., Cordeiro, V.K., Glienke, C., Maria Steffens, B.R., Hungria, M., GalliTerasawa, L.V. Morphological and genetic characterization of endophytic bacteria isolated from roots of different maize genotypes. Microb Ecol., 2013; 65:154-160.
  70. Khan, M.S., Zaidi, A., Ahemad, M., Oves, M., Wani, P.A. Plant growth promotion by phosphate solubilising fungi – Current perspective. Arch Agron Soil Sci., 2010; 56: 73-98.
  71. Richardson, A.E, Simpson, R.J. Soil microorganisms mediating phosphorus availability. Plant Physiol., 2011; 156:989-996.
  72. Kaur, H., Kaur, J., Gera, R. Plant Growth Promoting Rhizobacteria: A Boon to Agriculture. J. Cell Sci. Biotechnol., 2016; 5: 17-22.
  73. Goldstein, A.H. Bioprocessing of Rock Phosphate Ore: Essential Technical Considerations for the Development of a Successful Commercial Technology. New Orleans, USA: IFA technical conference. 2001.
  74. Egamberdiyeva, D., Qarshieva, , Davranov, K. Growth and yield of soybean varieties inoculated with Bradyrhizobium spp. in N-deficient calcareous soils. Biol. Fert. Soils., 2004; 40:144-146.
  75. Rodríguez, H., Fraga, R., Gonzalez, T., Bashan, Y. Genetics of phosphate solubilisation and its potential applications for improving plant growth-promoting bacteria. Plant Soil., 2006; 287:15-21.
  76. Hider, R.C., Kong, X. Chemistry and Biology of Siderophores. Prod. Rep., 2010; 27(5): 637-657.
  77. Mohandass C. Bacterial Siderophores and their Biotechnological Applications Marine Microbiology: Facts and Opportunities. 2004:169
  78. Fernandez V, Ebert G, Winkelmann G. The use of microbial siderophores for foliar iron application studies. Plant Soil., 2005; 272:245–252.
  79. Khan, M.S., Zaidi, A., Wani, P.A., Oves, M. Role of plant growth promoting rhizobacteria in the remediation of metal contaminated soils. Environ Chem Lett., 2009; 7 (1): 1–19.
  80. Rajkumar, M., Ae, N., Prasad, M.N.V., Freitas, H. Potential of siderophore-producing bacteria for improving heavy metal phytoextraction. Trends in Biotechnol., 2010; 28 (3):142-148.
  81. Murugappan, R.M., Aravinth, A., Rajaroobia, R., Karthikeyan, M., Alamelu, M.R. Optimization of MM9 Medium Constituents for Enhancement of Siderophoregenesis in Marine Pseudomonas putida Using Response Surface Methodology. Indian .J. Microbiol., 2012; 52 (3): 433–441.
  82. Wittenwiler, M. Mechanisms of Iron Mobilization by Siderophores. 2007:1-22.
  83. Kraemer, S.M., Crowley, D., Kretzschmar, R.Siderophores in plant iron acquisition: Geochemical aspects. Agron., 2006; 91: 1–46.
  84. Neilands, J.B. Iron absorption and transport in microorganisms. Rev. Nutr., 1981; 1: 27–46.
  85. Crowley, D.E, Wang, Y.C., Reid, C.P.P., Szaniszlo, P.J. Mechanism of iron acquisition from siderophores by microorganisms and plants. Plant Soil., 1991; 130 (1-2): 179-198.
  86. Saharan, B.S., Nehra, V. Plant Growth Promoting Rhizobacteria: A Critical Review. Life Sci Med Res., 2011; 21:1-30.
  87. Krewulak, K.D., Vogel, H.J. Structural biology of bacterial iron uptake. Biochim.Biophys. Acta., 2008; 1778: 1781–1804.
  88. P, Abdullah, R., Khadiran, T., Ismail. S, Boyce, A.N. Role of Plant Growth Promoting Rhizobacteria in Agricultural Sustainability—A Review. Molecules., 2016; 21: 573: 1-17.
  89. Masalha, J., Kosegarten, H., Elmaci, O., Mengel, K. The Central role of Microbial activity for iron acquisition in maize and sunflower. Fertil. Soil., 2000; 30 (5) : 433–439.
  90. Neubauer, U., Furrer, G., Kayser, A., Schulin, R., 2000. Siderophores, NTA, citrate: potential soil amendments to enhance heavy metal mobility in phytoremediation. J. Phytoremediation. 2 (4), 353–368.
  91. Andrews, S.C., Robinson, A.K., Rodríguez-Quiñones, F. Bacterial iron homeostasis. FEMS Microbiol Rev., 2003; 27(2-3):215-37.
  92. George, E. F., Machakova, I., Zazimalova, E .Plant Growth Regulators. I: Auxins, their Analogues and Inhibitors In: Plant Propagation by Tissue Culture. (George, EF, Hall, MA, Deklerk, GJ, ed.). Dordrecht, Netherlands: Springer, 2008; 175–204.
  93. F., Kostermans. D.G.F.R. Heteroauxin als Stoffwechselprodukt niederer pflanzlicher Organismen, Isolierung aus Hefe. Z Phys Chem., 1934; 228:113–121.
  94. Went, F.W., Thimann, K.V. , New York: The Macmillan Company. 1937; pp 1-256.
  95. Woodward, A.W., Bartel, B. Auxin: regulation, action, and interaction. Bot., 2005; 95:707–735.
  96. Teale, W.D., Paponov, I.A., Palme. K. Auxin in action: signalling, transport and the control of plant growth and development. Rev. Mol. Cell Biol., 2006; 7: 847–859.
  97. Ahemad, M., Kibret, M. Mechanisms and applications of plant growth promoting rhizobacteria: Current perspective. King Saud Univ.Sci., 2014; 26 (1):1-20.
  98. Dilfuza, E. Indole-Acetic Acid Production by Root Associated Bacteria and its Role in Plant Growth and Development. In: Auxins: Structure, Biosynthesis and Functions (Andrew, HK, Michelle, DF, ed.). Nova Science Publishers, 2011; pp1-13.
  99. Spaepen, S., Vanderleyden, J. Auxin and Plant-Microbe Interactions. Cold Spring Harb.Perspaect Biol., 2011; 3(4):1-13.
  100. Patten, C.L., Glick, B.R. Bacterial biosynthesis of indole-3-acetic acid. J.Microbiol., 1996; 42 (3):207–220.
  101. Glickmann, E., Gardan, L., Jacquet, S., Hussain, S., Elasri, M., Petit, A., Dessaux, Y. Auxin production is a common feature of most pathovars of Pseudomonas syringae. Mol Plant–Microbe Interact ., 1998; 11: 156–162.
  102. Spaepen, S., Vanderleyden, J., Remans.R. Indole-3-acetic acid in microbial and microorganism-plant signaling. FEMS Microbiol Rev., 2007; 31: 425–448.
  103. Lambrecht, M., Okon, Y., Broek, A.V., Vanderleyden, J. Indole-3-acetic acid: a reciprocal signalling molecule in bacteria – plant interactions. Trends Microbiol. 2000; 8 (7): 298-300.
  104. Dobbelaere, S., Croonenborghs, A., Thys, A., Ptacek, D., Vanderleyden, J., Dutto, P., Labandera Gonzalez, C., Caballero-Mellado, J., Anguirre, J.F., Kapulnik, Y., Brener, S., Burdman, S., Kadouri, D., Sarig, S., Okon, Y. Response of agronomically important crops to inoculation with Azospirillum. J. Plant Physiol., 2001; 28: 871-879.
  105. Zahir A., Abbas S. A., Khalid M., Arshad M.  Structure dependent microbially derived plant hormones by improving growth of maize seedlings. J. Biol. Sci., 2000; 3:289–291.
  106. Patten, C.L., Glick, B., Role of Pseudomonas putida indole acetic acid in development of the host plant root system. Environ. Microbiol., 2002; 68 (8): 3795-3801.
  107. Peyvandi, M., Farahani, F., Hussein, M., Noormohamadi, Z., Ataii, S., Asgharzadi, A. Pseudomonas fluorescens and its ability to promote root formation of olive microshoots. Int J Plant Prod. , 2010; 4 (1): 63-66.
  108. Ghosh, S., Sengupta, C., Maiti, T.K., Basu, P.S. Production of 3- Indolylacetic acid in root nodules and Culture by a Rhizobium species isolated from root nodules of the Leguminous pulse Phaseolus mungo. Folia Microbiologica. 2008; 53 (4), 351-355.
  109. Khare, E., Arora, N.K. Effect of indole-3-acetic acid (IAA) produced by Pseudomonas aeruginosa in suppression of charcoal rot disease of chickpea. Microbiol., 2010; 61 (1): 64-68.
  110. Patil, N.B., Gajbhiye, M., Ahiwale, S.S., Gunjal, A.P., Kapadnis, B.P. Optimization of Indole 3-acetic acid (IAA) production by Acetobacter diazotrophic L1 isolated from Sugarcane. J. Environ. Sci., 2011; 2 (1): 295-302.
  111. Dazzo, F.B., Yanni, Y.G., Rizk, R., De Bruijn, F.J., Rademaker, J., Squartini, A., Corich, V., Mateos, P., Martinez-Molina, E. Progress in multinational collaborative studies on the beneficial association between Rhizobium Ieguminosarum by trifolii and rice. In: The quest for nitrogen fixation in rice (Ladha, JK, Reddy, PM, ed). Philippines: IRR1, Los Banos, 2000; pp 167–189.
  112. Tsavkelova, E.A., Klimova, S.Y., Cherdyntseva, T.A., Netrusov, A.I. Microbial producers of plant growth stimulators and their practical use: a review. Biochem. Microbiol., 2006; 42 (2): 117–126.
  113. Ruanpanun, P., Tangchitsomkid, N., Hyde, K.D., Lumyong, S. Actinomycetes and fungi isolated from plant-parasitic nematode infested soils: screening of the effective biocontrol potential, indole-3-acetic acid and siderophore production. World J Microbiol Biotechnol., 2010; 26 (9): 1569–1578.
  114. Sarwar, M., Kremer, R.J. Determination of bacterially derived auxins using a microplate method. Lett Appl Microbiol. , 1995; 20 (5): 282-285.
  115. Kravchenko, L.V., Azareva, T.S., Makarova, N.M., Tikhonovich, I.A. The effect of tryptophan in plant root exudates on the phytostimulating activity of rhizobacteria. Microbiol., 2004; 73: 156-158.
  116. Kamilova F, Kravchenko LV, Shaposhnikov AI, Azarova T, Makarova N, Lugtenberg B. Organic acids, sugars, and L-tryptophane in exudates of vegetables growing on stonewool and their effects on activities of rhizosphere bacteria. Mol Plant-Microbe Interact., 2006; 19 (3):250– 256.
  117. Ghosh, S., Basu, P.S. Production and metabolism of indole acetic acid in roots and root nodules of Phaseolus mungo. Microbiol Res., 2006; 161: 362–366.
  118. Dullart, J. The bioproduction of indole-3-acetic acid and related compound in root nodules and roots of Lupinus luteus and by its rhizobial symbiont. Acta Bot Neerl., 1970; 19:573-615.
  119. Mano, Y., Nemoto, K.  The pathway of auxin biosynthesis in plants. J Exp Bot., 2012; 63: 2853–2872.
  120. Werner, T., Motyka, V., Laucou, V., Smets, R., Onckelen, H.V. Schmülling, T. Cytokinin-Deficient Transgenic Arabidopsis Plants Show Multiple Developmental Alterations Indicating Opposite Functions of Cytokinins in the Regulation of Shoot and Root Meristem Activity. Plant Cell., 2003; 15: 2532–2550.
  121. Salisbury, F.B., Ross, C.W. Hormones and Plant Regulators: Auxins and Gibberellins. In: Plant Physiology (Bressan, RA, Handa, AK, ed.). Belmont, California: Wadsworth Publishing Company, 1992: pp 357-381.
  122. Arshad, M., Frankenberger, W.T. Jr. Microbial production of plant growth regulators. In: Soil Microbial Ecology (Frankenberger, Jr. ed). New York: Dekker, 1993; pp 307–347.
  123. Nieto, K.F., Frankenberger, W.T. Jr. Microbial production of cytokinins .In: Soil Biochemistry (Bollag, JM, Stotzky, G. ed.). New York: Dekker, 1990; pp 191–248.
  124. Gutierrez-Manero F.J., Ramos-Solano, B., Probanza, A., Mehouachi, J., Tadeo, F.R., Talon, M. The plant growth-promoting rhizobacteria Bacillus licheniformis produce high amounts of physiologically active gibberillins. Physiologia Plantarum., 2001; 111: 206-211.
  125. Timmusk, S., Nicander, B., Granhall, U., Tillberg, E. Cytokinin production by Paenibacillus polymyxa. Soil Biol. Biochem., 1999; 31:1847–1852.
  126. Perrig D., Boiero M. L., Masciarelli O. A., Penna C., Ruiz O. A., Cassán F. D. Plant-growth-promoting compounds produced by two agronomically important strains of Azospirillum brasilense, and implications for inoculant formulation. Microbiol. Biotechnol., 2007; 75: 1143–1150.
  127. Frankenberger, J.W.T., Arshad, M., Microbial synthesis of auxins. In: Phytohormones in soils (Frankenberger, WT, Arshad, M, ed.). New York: Marcel Dekker, 1995; pp 35–71.
  128. Salisbury, F.B. The role of plant hormones. In: Plant–Environment Interactions (Wilkinson, RE, ed.). New York: Marcel Dekker. 1994; pp 39–81.
  129. MacMillan, J. Occurrence of gibberellins in vascular plants, fungi, and bacteria. J Plant Growth Regul., 2002; 20:387–442.
  130. Bottini R., Cassán F., Piccoli P. Gibberellin production by bacteria and its involvement in plant growth promotion and yield increase. Microbiol. Biotechnol., 2004; 65: 497–503.
  131. Tien, T.M., Gaskins, M.H., Hubbell, D.H. Plant Growth Substances Produced by Azospirillum brasilense and their Effect on the Growth of Pearl Millet (Pennisetum americanum). Appl Environ Microbiol., 1979; 37(5):1016-1024.
  132. Williams, P.M., de Mallorca, M.S. Abscisic acid and gibberellin-like substances in roots and root nodules of Glycine max. Plant Soil, 1982; 65(1): 19–26.
  133. Joo, G.J., Kin, Y.M., Kim, J.T., Rhee, I.K., Kim, J.H., Lee, I.J. Gibberellins-producing rhizobacteria increase endogenous gibberellins content and promote growth of red peppers. Microbiol., 2005; 43: 510–515.
  134. Dangar, T.K., Basu, P.S. Studies on plant growth substances, IAA metabolism and nitrogenase activity in root nodules of Phaseolus aureus Roxb. var. mungo. Biologia Plantarum., 1987; 29:350–354.
  135. Dobbelaere, S., Vanderleyden, J., Okon, Y. Plant growth promoting effects of diazotrophs in the rhizosphere. Crit Rev Plant Sci., 2003; 22:107–149.
  136. Boiero, L., Perrig, D., Masciarelli, O., Penna, C., Cassan, F., Luna, V. Phytohormone production by three strains of Bradyrhizobium japonicum and possible physiological and technological implications. Microbiol. Biotechnol., 2007; 74:874–880.
  137. Saleem, M., Arshad, M., Hussain, S., Bhatti, A.S. Perspective of plant growth promoting rhizobacteria (PGPR) containing ACC deaminase in stress agriculture. Ind. Microbiol. Biotechnol., 2007; 34 (10):635–648.
  138. Li, Q., Saleh-Lakha, S., Glick, B.R. The effect of native and ACC deaminase-containing Azospirillum brasilense Cd1843 on the rooting of carnation cuttings. Can J Microbiol ., 2005; 51:511–514.
  139. Chen, L.,Dodd, I.C., Theobald, J.C., Belimov, A.A.,   Davies, W.J. The rhizobacterium Variovorax paradoxus 5C-2, containing ACC deaminase, promotes growth and development of Arabidopsis thaliana via an ethylene-dependent pathway. Exp.Bot., 2013; 64 (6):1565–1573.
  140. Martinez-Viveros, O., Jorquera, M., Crowley, D.E., Gajardo, G., Mora, M.L. Mechanisms and practical considerations involved in plant growth promotion by rhizobacteria. Soil Sci. Plant Nutr., 2010; 10: 293-319.
  141. Glick, B.R.,   Penrose, D.M.,   Li, J. A model for the lowering of plant ethylene concentrations by plant growth promoting bacteria. J Theor Biol., 1998; 190: 63-68
  142. Mayak, S., Tirosh, T., Glick, B.R. Plant growth-promoting bacteria confer resistance in tomato plants to salt stress. Plant Physiol Biochem., 2004; 42 (6): 565-572.
  143. Govindasamy, V., Senthilkumar, M., Upendra-Kumar, A. K. PGPR-biotechnology for management of abiotic and biotic stresses in crop plants. In: Potential microorganisms for sustainable agriculture (Maheshwari DK, Dubey RC, ed.). New Delhi: IK International, 2008; pp 26–48.
  144. Ghosh, S., Penterman, J.N., Little, R.D., Chavez, R., Glick, B.R. Three newly isolated plant growth-promoting bacilli facilitate the growth of canola seedlings. Plant Physiol Biochem., 2003; 41: 277-281.
  145. J., Glick, B.R. Transcriptional regulation of the Enterobacter cloacae UW4 1-aminocyclopropane-1-carboxylate (ACC) deaminase gene (acdS). Can J Microbiol., 2001; 47:359–367.
  146. Duan, J., Müller, K.M., Charles, T.C., Vesely, S., Glick, B.R. 1-Aminocyclopropane-1- carboxylate (ACC) deaminase genes in Rhizobia from southern Saskatchewan. Microb Ecol., 2009; 57:423–436.
  147. Hafeez, F.Y., Yasmin, S.,  Ariani, D.,  Rahman, M.,  Zafar, Y.,  Malik, K.A. Plant growth-promoting bacteria as biofertilizer. Sustain. Dev., 2006; 26:143–150.
  148. Narayanasamy, P. Molecular Biology in Plant Pathogenesis and Disease Management. In: Disease Development. India: Springer, 2008: pp 7-195.
  149. Reddy, P.P. Plant growth promoting rhizobacteria (PGPR). In: Recent advances in crop protection. India: Springer, 2013; pp 131–145.
  150. Duffy, B. Pathogen self-defense: Mechanisms to counteract microbial antagonism. Ann Rev Phytopathol., 2003; 41:501-38.
  151. Maksimov, Abizgil’dina, R.R., Pusenkova, L.I. Plant growth promoting rhizobacteria as alternative to chemical crop protectors from pathogens (Review). Appl Biochem Microbiol ., 2011; 47:333-345.
  152. de Souza, J.T., Weller, D.M., Raaijmakers, J.M. Frequency, diversity and activity of 2, 4-diacetylphloroglucinol producing fluorescent Pseudomonas in Dutch take-all decline soils. Phytopathology., 2003; 93: 54-63.
  153. Neeraja, C., Anil, K., Purushotham, P., Suma, K., Sarma, P., Moerschbacher, B.M., Podile, A.R. Biotechnological approaches to develop bacterial chitinases as a bioshield against fungal diseases of plants. Crit Rev Biotechnol., 2010; 30:231-241.
  154. Haran, S., Schickler, H., Chet, I. Molecular mechanisms of lytic enzymes involved in the biocontrol activity of Trichoderma harzianum. Microbiology., 1996; 142: 2321-233.
  155. Pitson, S. , Seviour, R. J., McDougall, B. M. Noncelluloytic fungal p-glucanases: their physiology and regulation. Enzyme Microb Techno., 1993; 15: 178-192.
  156. Ramamoorthy, V., Viswanathan, R., Raguchandar, J., Prakasham, T. Samiyappan, R. Induction of systemic resistance by plant growth promoting rhizobacteria in crop plants against pest and diseases. Crop Protection., 2001; 20: 1-11.
  157. Choudhary, D.K., Prakash, A., Johr, B. N. Induced systemic resistance (ISR) in plants: Mechanism of action. Indian J Microbiol. , 2007; 47(4): 289–297.
  158. Yan Z., Reddy M.S., Ryu C.M., Mc Inroy J.A., Wilson M., Kloepper J.W. Induced systemic protection against tomato late blight elicited by PGPR. Phytopathol., 2002; 92:1329–1333.
  159. Doornbos, R.F., Loon, L.C., Bakker, P.A.H.M. Impact of root exudates and plant defense signalling on bacterial communities in the rhizosphere. Sustain. Dev. 2012; 32: 227–243.
  160. Zhang, S., Thomas L. White, T.L., Martinez, M.C., McInroy, J.A., Kloepper, J.W., Klassen, W. Evaluation of plant growth-promoting rhizobacteria for control of Phytophthora blight on squash under greenhouse conditions. Biol Control., 2010; 53: 129–135.