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里氏木霉纤维素酶在含葡萄糖培养基上的生产。

Production of Trichoderma reesei cellulases on glucose-containing media.

作者信息

Nakari-Setälä T, Penttilä M

机构信息

VTT Biotechnology and Food Research, Espoo, Finland.

出版信息

Appl Environ Microbiol. 1995 Oct;61(10):3650-5. doi: 10.1128/aem.61.10.3650-3655.1995.

DOI:10.1128/aem.61.10.3650-3655.1995
PMID:7487002
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC167665/
Abstract

The filamentous fungus Trichoderma reesei was shown to secrete active cellobiohydrolase I and the endoglucanase I catalytic core domain into the culture medium when the fungus was grown on glucose-containing medium. The expression of the proteins was driven by the promoters of the elongation factor 1 alpha, tef1, and the unidentified gene for cDNA1. The cDNA1 promoter gave the best yields. The highest amounts of cellobiohydrolase I and the endoglucanase I core, being 50 to 100 mg/liter, accounted for more than half of the total protein secreted by the fungus. The levels obtained with the tef1 promoter were 20 to 50 times lower.

摘要

丝状真菌里氏木霉在含葡萄糖的培养基上生长时,会将活性纤维二糖水解酶I和内切葡聚糖酶I催化核心结构域分泌到培养基中。这些蛋白质的表达由延伸因子1α(tef1)的启动子和未鉴定的cDNA1基因的启动子驱动。cDNA1启动子的产量最高。纤维二糖水解酶I和内切葡聚糖酶I核心的最高产量为50至100毫克/升,占真菌分泌的总蛋白的一半以上。tef1启动子获得的产量低20至50倍。

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本文引用的文献

1
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
2
Specific binding sites in the alcR and alcA promoters of the ethanol regulon for the CREA repressor mediating carbon catabolite repression in Aspergillus nidulans.构巢曲霉中乙醇调节子的alcR和alcA启动子上的特异性结合位点,用于CREA阻遏物介导碳分解代谢物阻遏。
Mol Microbiol. 1993 Mar;7(6):847-57. doi: 10.1111/j.1365-2958.1993.tb01175.x.
3
Isolation of Trichoderma reesei genes highly expressed on glucose-containing media: characterization of the tef1 gene encoding translation elongation factor 1 alpha.里氏木霉在含葡萄糖培养基上高表达基因的分离:编码翻译延伸因子1α的tef1基因的特性分析
Gene. 1993 Dec 22;136(1-2):313-8. doi: 10.1016/0378-1119(93)90486-m.
4
Cloning, sequencing and enhanced expression of the Trichoderma reesei endoxylanase II (pI 9) gene xln2.
Mol Gen Genet. 1993 Dec;241(5-6):497-503. doi: 10.1007/BF00279891.
5
Transformation of Trichoderma reesei with the Hormoconis resinae glucoamylase P (gamP) gene: production of a heterologous glucoamylase by Trichoderma reesei.用树脂芽枝霉葡糖淀粉酶P(gamP)基因转化里氏木霉:里氏木霉生产异源葡糖淀粉酶
Curr Genet. 1993 Sep;24(3):223-8. doi: 10.1007/BF00351796.
6
Rapamycin selectively represses translation of the "polypyrimidine tract" mRNA family.雷帕霉素选择性抑制“多嘧啶序列”mRNA家族的翻译。
Proc Natl Acad Sci U S A. 1994 May 10;91(10):4441-5. doi: 10.1073/pnas.91.10.4441.
7
Characterization of the regulatory elements in the promoter of the human elongation factor-1 alpha gene.
J Biol Chem. 1994 Nov 25;269(47):29831-7.
8
A glucose-derepressed promoter for expression of heterologous products in the filamentous fungus Aspergillus nidulans.用于在丝状真菌构巢曲霉中表达异源产物的葡萄糖去阻遏启动子。
Biotechnology (N Y). 1993 Jul;11(7):815-8. doi: 10.1038/nbt0793-815.
9
Efficient production of antibody fragments by the filamentous fungus Trichoderma reesei.丝状真菌里氏木霉高效生产抗体片段
Biotechnology (N Y). 1993 May;11(5):591-5. doi: 10.1038/nbt0593-591.
10
Transformation by integration in Aspergillus nidulans.构巢曲霉中的整合转化
Gene. 1983 Dec;26(2-3):205-21. doi: 10.1016/0378-1119(83)90191-9.