Enzyme profiles and genotyping of Chaetomium globosum isolates from various substrates

被引:27
作者
Abdel-Azeem, A. M. [1 ]
Gherbawy, Y. A. [2 ,3 ]
Sabry, A. M. [4 ,5 ]
机构
[1] Suez Canal Univ, Fac Sci, Dept Bot & Microbiol, Systemat Mycol Lab, Ismailia 41522, Egypt
[2] South Valley Univ, Fac Sci, Dept Bot, Qena, Egypt
[3] Taif Univ, Fac Sci, Dept Biol Sci, At Taif 888, Saudi Arabia
[4] Taif Univ, Biotechnol & Genet Engn Unit, Sci Res Deanship, At Taif, Saudi Arabia
[5] Natl Res Ctr, Dept Cell Biol, Genet Engn & Biotechnol Div, Tahrir St, Dokki Giza 12622, Egypt
来源
PLANT BIOSYSTEMS | 2016年 / 150卷 / 03期
关键词
Cellulase; dendrogram; identification; internal transcribed spacer region; phylogentics; MOLECULAR CHARACTERIZATION; FUNGI; BIODIVERSITY; COMMUNITIES; SPECIFICITY; DIVERSITY;
D O I
10.1080/11263504.2014.984791
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
The genus Chaetomium is a rich source of novel and bioactive secondary metabolites of great importance. To date, a variety of more than 200 secondary metabolites belonging to diverse structural types have been discovered. Fungal enzymes are used in food, beverages, confectionaries, textiles, and leather industries to simplify the processing of raw materials. They are often more stable than enzymes derived from other sources. Ten isolates of Chaetomium globosum recovered and designated as TUCg1 to TUCg10 were identified by morphological and molecular biology means and submitted to the GenBank. These isolates were screened for extracellular enzymes such as amylase, cellulase, laccase, lipase, pectinases, protease and chitinase on solid media. All Chaetomium globosum isolates screened for potential enzymes showed amylolytic, cellulolytic, and proteolytic activities; six isolates were chitinolytic and laccase producers; and five and three isolates showed pectinolytic and lipolytic activities, respectively. The produced array of enzymes differed among isolates. Molecular techniques such as internal transcribed spacer (ITS) region sequencing and specific genes random primers polymerase chain reaction (SGRP-PCR) have shown high DNA polymorphism of Chaetomium globosum. In conclusion, SGRP-PCR is a rapid and valuable tool for assessment and characterization of genetic diversity of Chaetomium globosum, which suggests the use of this technique for identification of different fungal isolates.
引用
收藏
页码:420 / 428
页数:9
相关论文
共 58 条
[1]   Biodiversity of laccase producing fungi in Egypt [J].
Abdel-Azeem, A. M. ;
Salem, F. M. .
MYCOSPHERE, 2012, 3 (06) :900-920
[2]   The history, fungal biodiversity, conservation, and future perspectives for mycology in Egypt [J].
Abdel-Azeem, Ahmed M. .
IMA FUNGUS, 2010, 1 (02) :123-142
[3]   Molecular characterization of Chaetomium species using URP-PCR [J].
Aggarwal, Rashmi ;
Sharma, Vandana ;
Kharbikar, Lalit L. ;
Renu .
GENETICS AND MOLECULAR BIOLOGY, 2008, 31 (04) :943-946
[4]  
[Anonymous], 2005, J AGR TECHNOLOGY
[5]  
Bali R, 2003, THESIS ENV PUNJAB IN
[6]   Globosumones A-C, cytotoxic orsellinic acid esters from the sonoran desert endophytic fungus Chaetomium globosum [J].
Bashyal, BP ;
Wijeratne, EMK ;
Faeth, SH ;
Gunatilaka, AAL .
JOURNAL OF NATURAL PRODUCTS, 2005, 68 (05) :724-728
[7]   Cellulases and related enzymes in biotechnology [J].
Bhat, MK .
BIOTECHNOLOGY ADVANCES, 2000, 18 (05) :355-383
[8]   Marine natural products [J].
Blunt, John W. ;
Copp, Brent R. ;
Munro, Murray H. G. ;
Northcote, Peter T. ;
Prinsep, Michele R. .
NATURAL PRODUCT REPORTS, 2011, 28 (02) :196-268
[9]  
Castella G, 2002, SYST APPL MICROBIOL, V25, P74, DOI [10.1078/0723-2020-00094, 10.1078/0723202022528852]
[10]  
Czakaj J., 2003, Prace Instytutow i Laboratoriow Badawczych Przemyslu Spozywczego, V58, P74