Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2121
Title: Identification patterns of Trichoderma strains using morphological characteristics, phylogenetic analyses and lignocellulolytic activities
Authors: Asis, A 
Shahriar, SA 
Naher, L. 
Saallah, S 
Fatihah, HNN 
Kumar, V 
Siddiquee, S 
Keywords: Trichoderma;Morphology characters;Internal transcribed spacers;Translation elongation factor 1-α
Issue Date: Apr-2021
Journal: MOLECULAR BIOLOGY REPORTS 
Abstract: 
Trichoderma is a genus of soil-borne fungus with an abundance of reports of its economic importance in the agriculture industry. Thus, the correct identification of Trichoderma species is necessary for its commercial purposes. Globally, Trichoderma species are routinely identified from micro-morphological descriptions which can be tedious and prone to errors. Thus, we emphasize that the accurate identification of Trichoderma strains requires a three-pronged approach i.e. based on its morphological characteristics, multilocus gene sequences of the rDNA [internal transcribed spacer (ITS) 1 and 2 regions], translation elongation factor 1-alpha (TEF-1 alpha), Calmodulin (CAL) and its lignocellulolytic activities. We used this approach to identify a total of 53 Trichoderma strains which were isolated from a wet paddy field located at Tuaran, Sabah, Malaysia. The 53 strains were positively identified as belonging to three Trichoderma species, namely T. asperellum (43 strains), T. harzianum (9 strains), and T. reesei (one strain) on the basis of its morphological characteristics and multilocus gene sequences. Phylogenetic trees constructed based on the UPGMA method of the ITS 1 and 2 regions of the rDNA, TEF-1 alpha and CAL revealed three distinct groups with the T. asperellum, T. harzianum and T. reesei strains placed under the section of Trichoderma, Pachybasium and Longibrachiatum, respectively. In addition, the lignocellulolytic activities of the isolates were measured based on the diameters of the halo zones produced when degrading cellulose, lignin, and starch, respectively. This diagnostic assay can be used to identify Trichoderma as it produces polyphenol oxidase when Tannic Acid Media is used for the lignin test, endoglucanases when Jensen media is used for cellulose, and it hydrolyzes starch to glucose when the modified Melin-Nokrans media is used for the starch test. Accurate identification of Trichoderma species is needed as these strains can potentially be used as a biocontrol agent to prevent diseases and to increase yield in agriculture crops.
Description: 
Web of Science
URI: http://hdl.handle.net/123456789/2121
ISSN: 0301-4851
DOI: 10.1007/s11033-021-06321-0
Appears in Collections:Faculty of Agro Based Industry - Journal (Scopus/WOS)

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