ISSN: 0973-7510

E-ISSN: 2581-690X

Huimin Zhang1, Changlu Guo1, Hongkui He2, Kaiqiang Li1, Yuan Sun1, Qingwu Zhoub and Zhizhou Zhang1,2
1School of Marine Science and Technology, Lab for Personalized Nutrition and Food Safety, Marine Antifouling Engineering Technology Center of Shangdong Province, Harbin Institute of Technology, Weihai – 264 209, China.
2The GuJing Group, Bozhou, Anhui – 236 800, China.
J Pure Appl Microbiol. 2013;7(Spl. Edn.: November):601-610
© The Author(s). 2013
Received: 27/09/2013 | Accepted: 04/11/2013 | Published: 30/11/2013
Abstract

People have normally known little about microbial species in any natural complex microbial community, in which minor species have been paid less attention in the context of their functional roles in maintaining the community complexity. Proper quantification of such minor species shall be a prerequisite for functional studies. In this report, TA-cloning was used to decipher the structure of 12 GuJingGong liquor-making microbial community samples; 32 minor species in the microbial community were found to already have whole genome sequences,  and species-specific primers were designed and synthesized for real-time quantification polymerase chain reaction (QPCR). Among the 32 targets, 19 gave expected PCR results and then were emplyed to quantify 12 GuJingGong microbial community samples. Proper strategy for quantification of compositional structure of a complex microbial community was discussed.

Keywords

Complex microbial community, Minor species, Quantification, PCR, species-specific primer

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© The Author(s) 2013. Open Access. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License which permits unrestricted use, sharing, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.