ISSN: 0973-7510

E-ISSN: 2581-690X

Puttagunta Udaya Sri1, Gampala Kranthi2 and Pinnamaneni Rajasekhar1
1Centre for Biotechnology, Acharya Nagarjuna University, Nagarjuna Nagar, Guntur, India.
2Department of Biotechnology, Jagarlamudi Kuppuswamy Choudary College, Guntur-6, India.
J Pure Appl Microbiol. 2010;4(1):95-102
© The Author(s). 2010
Received: 18/10/2009 | Accepted: 24/12/2009 | Published: 30/04/2010
Abstract

The objective of the present study was to identify the cellulose degrading Trichoderma viride. Dilution plating was used to quantify the propagule numbers of Trichoderma, denaturing gradient gel electrophoresis (DGGE) and DNA sequence analysis were used to identify Trichoderma species. Trichoderma viride was identified based on the microscopic observations by Lactophenol cotton blue and scanning electron microscopy.
It was ultimately confirmed based on DGGE and DNA sequence analysis and finally concluded by BLAST analysis by constructing a phylogenetic tree.

Keywords

Trichoderma viride, Dilution plating, 18s RNA, BLAST

Article Metrics

Article View: 686

Share This Article

© The Author(s) 2010. 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.