The effect of specific growth rate on protein synthesis and secretion in the filamentous fungus Trichoderma reesei

被引:74
作者
Pakula, TM [1 ]
Salonen, K [1 ]
Uusitalo, J [1 ]
Penttilä, M [1 ]
机构
[1] VTT Biotechnol, FIN-02044 Espoo, Finland
来源
MICROBIOLOGY-SGM | 2005年 / 151卷
关键词
D O I
10.1099/mic.0.27458-0
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Trichoderma reesei was cultivated in chemostat cultures on lactose-containing medium. The cultures were characterized for growth, consumption of the carbon source and protein production. Secreted proteins were produced most efficiently at low specific growth rates, 0(.)022-0(.)033 h(-1), the highest specific rate of total protein production being 4(.)1 mg g(-1) h(-1) at the specific growth rate 0(.)031 h(-1). At low specific growth rates, up to 29% of the proteins produced were extracellular, in comparison to only 6-8% at high specific growth rates, 0(.)045-0(.)066 h(-1). To analyse protein synthesis and secretion in more detail, metabolic labelling of proteins was applied to analyse production of the major secreted protein, cellobiohydrolase I (CBHI, Cel7A). Intracellular and extracellular labelled CBHI was quantified and analysed for pl isoforms in two-dimensional gels, and the synthesis and secretion rates of the molecule were determined. Both the specific rates of CBHI synthesis and secretion were highest at low specific growth rates, the optimum being at 0(.)031 h(-1). However, at low specific growth rates the secretion rate/synthesis rate ratio was significantly lower than that at high specific growth rates, indicating that at low growth rates the capacity of cells to transport the protein becomes limiting. In accordance with the high level of protein production and limitation in the secretory capacity, the transcript levels of the unfolded protein response (UPR) target genes pdi1 and bip1 as well as the gene encoding the UPR transcription factor hac1 were induced.
引用
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页码:135 / 143
页数:9
相关论文
共 45 条
  • [1] BASSET J, 1987, VOGELS TXB QUANTITAT
  • [2] Biely P., 1998, Trichoderma and gliocladium, P25
  • [3] FOLDING OF INFLUENZA HEMAGGLUTININ IN THE ENDOPLASMIC-RETICULUM
    BRAAKMAN, I
    HOOVERLITTY, H
    WAGNER, KR
    HELENIUS, A
    [J]. JOURNAL OF CELL BIOLOGY, 1991, 114 (03) : 401 - 411
  • [4] Growth and alpha-amylase production by Aspergillus oryzae during continuous cultivations
    Carlsen, M
    Nielsen, J
    Villadsen, J
    [J]. JOURNAL OF BIOTECHNOLOGY, 1996, 45 (01) : 81 - 93
  • [5] LACTASE PRODUCTION IN CONTINUOUS CULTURE BY TRICHODERMA REESEI RUT-C30
    CASTILLO, FJ
    BLANCH, HW
    WILKE, CR
    [J]. BIOTECHNOLOGY LETTERS, 1984, 6 (09) : 593 - 596
  • [6] COMPARISON OF GROWTH AND MAINTENANCE PARAMETERS FOR CELLULASE BIOSYNTHESIS BY TRICHODERMA REESEI-C5 WITH SOME PUBLISHED DATA
    CHAUDHURI, BK
    SAHAI, V
    [J]. ENZYME AND MICROBIAL TECHNOLOGY, 1994, 16 (12) : 1079 - 1083
  • [7] COLLEN A, 2004, IN PRESS BIOTECHNOL
  • [8] Transcriptional regulation of biomass-degrading enzymes in the filamentous fungus Trichoderma reesei
    Foreman, PK
    Brown, D
    Dankmeyer, L
    Dean, R
    Diener, S
    Dunn-Coleman, NS
    Goedegebuur, F
    Houfek, TD
    England, GJ
    Kelley, AS
    Meerman, HJ
    Mitchell, T
    Mitchinson, C
    Olivares, HA
    Teunissen, PJM
    Yao, J
    Ward, M
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (34) : 31988 - 31997
  • [9] SYNTHESIS AND ASSEMBLY OF ADENOVIRUS 2 .I. POLYPEPTIDE SYNTHESIS, ASSEMBLY OF CAPSOMERES, AND MORPHOGENESIS OF VIRION
    HORWITZ, MS
    SCHARFF, MD
    MAIZEL, JV
    [J]. VIROLOGY, 1969, 39 (04) : 682 - &
  • [10] IIMEN M, 1996, MOL GEN GENET, V251, P451