Overproduction of β-1,6-glucanase in Trichoderma harzianum is controlled by extracellular acidic proteases and pH

被引:35
作者
Delgado-Jarana, J
Pintor-Toro, JA
Benítez, T
机构
[1] Univ Sevilla, Fac Biol, Dept Genet, E-41080 Seville, Spain
[2] CSIC, Inst Recursos Nat & Agrobiol, E-41080 Seville, Spain
来源
BIOCHIMICA ET BIOPHYSICA ACTA-PROTEIN STRUCTURE AND MOLECULAR ENZYMOLOGY | 2000年 / 1481卷 / 02期
关键词
beta-1,6-glucanase; protease; pH; enzyme production; proteolysis; Trichoderma harzianum;
D O I
10.1016/S0167-4838(00)00172-2
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
To produce high amounts of extracellular endo-beta-1,6-glucanase, we overexpressed the gene bgn16.2 from Trichoderma harzianum under the control of the pyruvate kinase gene promoter (pki) of T. reesei. Transcription of bgn16.2 gene increased under most conditions but not extracellular beta-1,6-glucanase levels. Relationship of extracellular BGN16.2 protein and presence of proteases was studied in order to maximize production. After changing the carbon and nitrogen sources and buffering the culture media at different pHs, four major proteases, the acidic ones being pH-regulated, were detected. Overexpression of BGN16.2 at low pH resulted in BGN16.2 degradation, due to the induction of aspartyl proteases and to instability at pH below 3. Maximal overproduction of BGN16.2 albeit pure was achieved in buffered medium, where pH-induced aspartyl proteases were absent or when some nitrogen sources, such as yeast extract, peptone or casein were substrate for these proteases. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:289 / 296
页数:8
相关论文
共 32 条
[21]   TRANSFORMATION OF TRICHODERMA-REESEI BASED ON HYGROMYCIN-B RESISTANCE USING HOMOLOGOUS EXPRESSION SIGNALS [J].
MACH, RL ;
SCHINDLER, M ;
KUBICEK, CP .
CURRENT GENETICS, 1994, 25 (06) :567-570
[22]  
MANTYLA A, 1998, TRICHODERMA GLIOCLAD, V2
[23]   Enhanced expression of endochitinase in Trichoderma harzianum with the cbh1 promoter of Trichoderma reesei [J].
MargollesClark, E ;
Harman, GE ;
Penttila, M .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (06) :2152-2155
[24]  
NAKARISETALA T, 1995, APPL ENVIRON MICROB, V61, P3650
[25]  
NELSON NJ, 1957, METHOD ENZYMOL, V3, P85
[26]   Expression and secretion of barley cysteine endopeptidase B and cellobiohydrolase I in Trichoderma reesei [J].
Nykanen, M ;
Saarelainen, R ;
Raudaskoski, M ;
Nevalainen, KMH ;
Mikkonen, A .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (12) :4929-4937
[27]   EFFICIENT PRODUCTION OF ANTIBODY FRAGMENTS BY THE FILAMENTOUS FUNGUS TRICHODERMA-REESEI [J].
NYYSSONEN, E ;
PENTTILA, M ;
HARKKI, A ;
SALOHEIMO, A ;
KNOWLES, JKC ;
KERANEN, S .
BIO-TECHNOLOGY, 1993, 11 (05) :591-595
[28]   A VERSATILE TRANSFORMATION SYSTEM FOR THE CELLULOLYTIC FILAMENTOUS FUNGUS TRICHODERMA-REESEI [J].
PENTTILA, M ;
NEVALAINEN, H ;
RATTO, M ;
SALMINEN, E ;
KNOWLES, J .
GENE, 1987, 61 (02) :155-164
[29]   CLONING, SEQUENCING AND ENHANCED EXPRESSION OF THE TRICHODERMA-REESEI ENDOXYLANASE-II (PI 9) GENE XLN2 [J].
SAARELAINEN, R ;
PALOHEIMO, M ;
FAGERSTROM, R ;
SUOMINEN, PL ;
NEVALAINEN, KMH .
MOLECULAR AND GENERAL GENETICS, 1993, 241 (5-6) :497-503
[30]  
Sambrook J., 2002, MOL CLONING LAB MANU