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
[11]   ISOLATION OF GENOMIC CLONES CONTAINING THE AMDS GENE OF ASPERGILLUS-NIDULANS AND THEIR USE IN THE ANALYSIS OF STRUCTURAL AND REGULATORY MUTATIONS [J].
HYNES, MJ ;
CORRICK, CM ;
KING, JA .
MOLECULAR AND CELLULAR BIOLOGY, 1983, 3 (08) :1430-1439
[12]  
Jeenes D J, 1991, Biotechnol Genet Eng Rev, V9, P327
[13]   The contribution of the O-glycosylated protein Pir2p/Hsp150 to the construction of the yeast cell wall in wild-type cells and β1,6-glucan-deficient mutants [J].
Kapteyn, JC ;
Van Egmond, P ;
Sievi, E ;
Van Den Ende, H ;
Makarow, M ;
Klis, FM .
MOLECULAR MICROBIOLOGY, 1999, 31 (06) :1835-1844
[14]   Retention of Saccharomyces cerevisiae cell wall proteins through a phosphodiester-linked beta-1,3-/beta-1,6-glucan heteropolymer [J].
Kapteyn, JC ;
Montijn, RC ;
Vink, E ;
delaCruz, J ;
Llobell, A ;
Douwes, JE ;
Shimoi, H ;
Lipke, PN ;
Klis, FM .
GLYCOBIOLOGY, 1996, 6 (03) :337-345
[15]   HIGH-FREQUENCY ONE-STEP GENE REPLACEMENT IN TRICHODERMA-REESEI .1. ENDOGLUCANASE-I OVERPRODUCTION [J].
KARHUNEN, T ;
MANTYLA, A ;
NEVALAINEN, KMH ;
SUOMINEN, PL .
MOLECULAR AND GENERAL GENETICS, 1993, 241 (5-6) :515-522
[16]   TRANSFORMATION OF TRICHODERMA-REESEI WITH THE CELLOBIOHYDROLASE-II GENE AS A MEANS FOR OBTAINING STRAINS WITH INCREASED CELLULASE PRODUCTION AND SPECIFIC ACTIVITY [J].
KUBICEKPRANZ, EM ;
GRUBER, F ;
KUBICEK, CP .
JOURNAL OF BIOTECHNOLOGY, 1991, 20 (01) :83-94
[17]   Glucose-induced secretion of Trichoderma reesei xylanases [J].
Kurzatkowski, W ;
Torronen, A ;
Filipek, J ;
Mach, RL ;
Herzog, P ;
Sowka, S ;
Kubicek, CP .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1996, 62 (08) :2859-2865
[18]   CLEAVAGE OF STRUCTURAL PROTEINS DURING ASSEMBLY OF HEAD OF BACTERIOPHAGE-T4 [J].
LAEMMLI, UK .
NATURE, 1970, 227 (5259) :680-+
[19]   MOLECULAR CHARACTERIZATION AND HETEROLOGOUS EXPRESSION OF AN ENDO-BETA-1,6-GLUCANASE GENE FROM THE MYCOPARASITIC FUNGUS TRICHODERMA-HARZIANUM [J].
LORA, JM ;
DELACRUZ, J ;
LLOBELL, A ;
BENITEZ, T ;
PINTORTORO, JA .
MOLECULAR & GENERAL GENETICS, 1995, 247 (05) :639-645
[20]  
LOWRY OH, 1951, J BIOL CHEM, V193, P265