Cell wall-degrading isoenzyme profiles of Trichoderma biocontrol strains show correlation with rDNA taxonomic species

被引:43
作者
Sanz, L
Montero, M
Grondona, I
Vizcaíno, J
Llobell, A
Hermosa, R
Monte, E [1 ]
机构
[1] Univ Salamanca, Ctr Hispano Luso Invest Agrarias, Dept Genet & Microbiol, Salamanca 37007, Spain
[2] Newbiotechn SA NBT, Seville 41092, Spain
[3] Univ Seville, CSIC, IBVF CIC Isla Cartuja, Seville 41092, Spain
关键词
Trichoderma; biocontrol agent; lytic enzymes; genetic diversity;
D O I
10.1007/s00294-004-0532-6
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Trichoderma is known for being the most frequently used biocontrol agent in agriculture. A fundamental part of the Trichoderma antifungal system relies on a series of genes coding for a variety of extracellular lytic enzymes. Characterization of the polymorphism between five putative isoenzymatic activities [beta-1,3-glucanase (EC 3.2.1.39, EC 3.2.1.58), beta-1,6- glucanase ( EC 3.2.1.75), cellulase ( EC 3.2.1.4; EC 3.2.1.21, EC 3.2.1.91), chitinase ( EC 3.2.1.30, EC 3.2.1.52), protease ( EC 3.4.11; EC 3.4.13 - 19; EC 3.4.21 - 24, EC 3.4.99)] was carried out using 18 strains from three sections of Trichoderma. Of these, seven strains were from T. sect. Pachybasium, nine from T. sect. Trichoderma and two from T. sect. Longibrachiatum. Thirty-seven different alleles in total were identified: 13 for beta-1,3-glucanase, four for beta-1,6- glucanase, three for cellulase, eight for chitinase and nine for protease activity. A dendrogram ( constructed by the unweighted pair group method with arithmetic averages) based on isoenzymatic data separated the 18 strains into three main enzymatic groups: T. harzianum, T. atroviride/T. viride/T. koningii and T. asperellum/ T. hamatum/T. longibrachiatum. Isoenzymatic groupings obtained from biocontrol strains are discussed in relation to their phylogenetic location, based on their sequence of internal transcribed spacer 1 in ribosomal DNA and their antifungal activities.
引用
收藏
页码:277 / 286
页数:10
相关论文
共 60 条
[51]   MORPHOLOGICAL AND MACROMOLECULAR CHARACTERIZATION OF HYPOCREA-SCHWEINITZII AND ITS TRICHODERMA ANAMORPH [J].
SAMUELS, GJ ;
PETRINI, O ;
MANGUIN, S .
MYCOLOGIA, 1994, 86 (03) :421-435
[52]   Detection of β-1,6-glucanase isozymes from Trichoderma strains in sodium dodecyl sulphate polyacrylamide gel electrophoresis and isoelectrofocusing gels [J].
Soler, A ;
de la Cruz, J ;
Llobell, A .
JOURNAL OF MICROBIOLOGICAL METHODS, 1999, 35 (03) :245-251
[53]   EVALUATION OF PHENETIC SPECIES AND PHYLOGENETIC-RELATIONSHIPS IN THE GENUS TRICHODERMA BY CLADISTIC-ANALYSIS OF ISOZYME POLYMORPHISM [J].
STASZ, TE ;
NIXON, K ;
HARMAN, GE ;
WEEDEN, NF ;
KUTER, GA .
MYCOLOGIA, 1989, 81 (03) :391-403
[54]   Isolation and characterization of PRA1, a trypsin-like protease from the biocontrol agent Trichoderma harzianum CECT 2413 displaying nematicidal activity [J].
Suarez, B ;
Rey, M ;
Castillo, P ;
Monte, E ;
Llobell, A .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 2004, 65 (01) :46-55
[55]   The CLUSTAL_X windows interface: flexible strategies for multiple sequence alignment aided by quality analysis tools [J].
Thompson, JD ;
Gibson, TJ ;
Plewniak, F ;
Jeanmougin, F ;
Higgins, DG .
NUCLEIC ACIDS RESEARCH, 1997, 25 (24) :4876-4882
[56]   DETECTION AND QUANTIFICATION OF N-ACETYL-BETA-D-GLUCOSAMINIDASE, CHITOBIOSIDASE, AND ENDOCHITINASE IN SOLUTIONS AND ON GELS [J].
TRONSMO, A ;
HARMAN, GE .
ANALYTICAL BIOCHEMISTRY, 1993, 208 (01) :74-79
[57]   Expression regulation of the endochitinase chit36 from Thichoderma asperellum (T-harzianum T-203) [J].
Viterbo, A ;
Montero, M ;
Ramot, O ;
Friesem, D ;
Monte, E ;
Llobell, A ;
Chet, I .
CURRENT GENETICS, 2002, 42 (02) :114-122
[58]   Significance of lytic enzymes from Trichoderma spp. in the biocontrol of fungal plant pathogens [J].
Viterbo, A ;
Ramot, O ;
Chernin, L ;
Chet, I .
ANTONIE VAN LEEUWENHOEK INTERNATIONAL JOURNAL OF GENERAL AND MOLECULAR MICROBIOLOGY, 2002, 81 (1-4) :549-556
[59]   APPLICATION OF ENZYME ELECTROPHORESIS FOR THE IDENTIFICATION OF ISOLATES IN TRICHODERMA-HARZIANUM [J].
ZAMIR, D ;
CHET, I .
CANADIAN JOURNAL OF MICROBIOLOGY, 1985, 31 (06) :578-580
[60]   USE OF THE RAPD PROCEDURE FOR THE IDENTIFICATION OF TRICHODERMA STRAINS [J].
ZIMAND, G ;
VALINSKY, L ;
ELAD, Y ;
CHET, I ;
MANULIS, S .
MYCOLOGICAL RESEARCH, 1994, 98 :531-534