Amino acid supplementation, controlled oxygen limitation and sequential double induction improves heterologous xylanase production by Pichia stipitis

被引:24
作者
Görgens, JF
Passoth, V [1 ]
van Zyl, WH
Knoetze, JH
Hahn-Hägerdal, M
机构
[1] Lund Univ, Dept Appl Microbiol, Lund, Sweden
[2] Univ Stellenbosch, Dept Proc Engn, ZA-7600 Stellenbosch, South Africa
[3] Swedish Univ Agr Sci, Dept Microbiol, Uppsala Genet Ctr, S-75007 Uppsala, Sweden
[4] Univ Stellenbosch, Dept Microbiol, ZA-7600 Stellenbosch, South Africa
关键词
Pichia stipitis; heterologous protein expression; regulated promoter; aeration; endo-beta-1,4-xylanase;
D O I
10.1016/j.femsyr.2004.12.003
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Heterologous endo-beta-1,4-xylanase was produced by Pichia stipitis under control of the hypoxia-inducible PsADH2-promoter in a high-cell-clensity culture. After promoter induction by a shift to oxygen limitation, different aeration rates (oxygen transfer rates) were applied while maintaining oxygen-limitation. Initially, enzyme production was higher in oxygen-limited cultures with high rates of oxygen transfer, although the maximum xylanase activity was not significantly influenced. Amino acid supplementation increased the production of the heterologous endo-beta-1,4-xylanase significantly in highly aerated oxygen-limited cultures, until glucose was depleted. A slight second induction of the promoter was observed in all cultures after the glucose had been consumed. The second induction was most obvious in amino acid-supplemented cultures with higher oxygen transfer rates during oxygen limitation. When such oxygen-limited cultures were shifted back to fully aerobic conditions, a significant re-induction of heterologous endo-beta-1,4-xylanase production was observed. Re-induction was accompanied by ethanol consumption. A similar protein production pattern was observed when cultures were first grown on ethanol as sole carbon source and subsequently glucose and oxygen limitation were applied. Thus, we present the first expression system in yeast with a sequential double-inducible promoter. (c) 2004 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:677 / 683
页数:7
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