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本文引用的文献

1
Reduction of Lactose in Milk by Purified Lactase Produced by Kluyveromyces lactis.乳酸克鲁维酵母产生的纯化乳糖酶降低牛奶中乳糖的含量
J Food Prot. 1989 Jan;52(1):30-34. doi: 10.4315/0362-028X-52.1.30.
2
Heterologous protein secretion directed by a repressible acid phosphatase system of Kluyveromyces lactis: characterization of upstream region-activating sequences in the KIPHO5 gene.乳酸克鲁维酵母可阻遏酸性磷酸酶系统指导的异源蛋白分泌:KIPHO5基因上游区域激活序列的特性分析
Appl Environ Microbiol. 1998 Jul;64(7):2403-8. doi: 10.1128/AEM.64.7.2403-2408.1998.
3
Analysis of Pichia pastoris components in recombinant human serum albumin by immunological assays and by HPLC with pulsed amperometric detection.采用免疫分析法和带脉冲安培检测的高效液相色谱法分析重组人血清白蛋白中的毕赤酵母成分。
Anal Chem. 1998 Jan 15;70(2):425-9. doi: 10.1021/ac970596h.
4
The KIPHO5 gene encoding a repressible acid phosphatase in the yeast Kluyveromyces lactis: cloning, sequencing and transcriptional analysis of the gene, and purification and properties of the enzyme.编码乳酸克鲁维酵母中一种可阻遏酸性磷酸酶的KIPHO5基因:该基因的克隆、测序与转录分析,以及该酶的纯化与性质研究
Microbiology (Reading). 1997 Aug;143 ( Pt 8):2615-2625. doi: 10.1099/00221287-143-8-2615.
5
The 'petite-negative' yeast Kluyveromyces lactis has a single gene expressing pyruvate decarboxylase activity.“小菌落阴性”酵母乳酸克鲁维酵母有一个表达丙酮酸脱羧酶活性的基因。
Mol Microbiol. 1996 Jan;19(1):27-36. doi: 10.1046/j.1365-2958.1996.346875.x.
6
Two mitochondrial alcohol dehydrogenase activities of Kluyveromyces lactis are differently expressed during respiration and fermentation.乳酸克鲁维酵母的两种线粒体乙醇脱氢酶活性在呼吸和发酵过程中的表达有所不同。
Mol Gen Genet. 1995 Dec 20;249(6):665-72. doi: 10.1007/BF00418036.
7
The yeast Kluyveromyces lactis as an efficient host for heterologous gene expression.乳酸克鲁维酵母作为异源基因表达的高效宿主。
Antonie Van Leeuwenhoek. 1993;64(2):187-201. doi: 10.1007/BF00873027.
8
Physiological approach to heterologous human serum albumin production by Kluyveromyces lactis in chemostat culture.乳酸克鲁维酵母在恒化器培养中生产异源人血清白蛋白的生理学方法。
Yeast. 1994 Oct;10(10):1297-303. doi: 10.1002/yea.320101006.
9
Expression and purification of a truncated macrophage colony stimulating factor in Kluyveromyces lactis.截短型巨噬细胞集落刺激因子在乳酸克鲁维酵母中的表达与纯化
Biochem Mol Biol Int. 1994 Sep;34(2):419-27.
10
Development of high-cell-density fermentation for heterologous interleukin 1 beta production in Kluyveromyces lactis controlled by the PHO5 promoter.在PHO5启动子控制下,用于乳酸克鲁维酵母中异源白细胞介素1β生产的高细胞密度发酵的开发。
Appl Microbiol Biotechnol. 1994 May;41(3):324-9. doi: 10.1007/BF00221227.

利用乳酸克鲁维酵母中的KlADH4启动子进行乙醇依赖性重组人血清白蛋白的生产。

Use of the KlADH4 promoter for ethanol-dependent production of recombinant human serum albumin in Kluyveromyces lactis.

作者信息

Saliola M, Mazzoni C, Solimando N, Crisà A, Falcone C, Jung G, Fleer R

机构信息

Department of Cell and Developmental Biology, Pasteur Institute-Cenci Bolognetti Foundation, University of Rome "La Sapienza," 00185 Rome, Italy.

出版信息

Appl Environ Microbiol. 1999 Jan;65(1):53-60. doi: 10.1128/AEM.65.1.53-60.1999.

DOI:10.1128/AEM.65.1.53-60.1999
PMID:9872759
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC90982/
Abstract

KlADH4 is a gene of Kluyveromyces lactis encoding a mitochondrial alcohol dehydrogenase activity which is specifically induced by ethanol. The promoter of this gene was used for the expression of heterologous proteins in K. lactis, a very promising organism which can be used as an alternative host to Saccharomyces cerevisiae due to its good secretory properties. In this paper we report the ethanol-driven expression in K. lactis of the bacterial beta-glucuronidase and of the human serum albumin (HSA) genes under the control of the KlADH4 promoter. In particular, we studied the extracellular production of recombinant HSA (rHSA) with integrative and replicative vectors and obtained a significant increase in the amount of the protein with multicopy vectors, showing that no limitation of KlADH4 trans-acting factors occurred in the cells. By deletion analysis of the promoter, we identified an element (UASE) which is sufficient for the induction of KlADH4 by ethanol and, when inserted in the respective promoters, allows ethanol-dependent activation of other yeast genes, such as PGK and LAC4. We also analyzed the effect of medium composition on cell growth and protein secretion. A clear improvement in the production of the recombinant protein was achieved by shifting from batch cultures (0.3 g/liter) to fed-batch cultures (1 g/liter) with ethanol as the preferred carbon source.

摘要

KlADH4是乳酸克鲁维酵母的一个基因,编码一种线粒体乙醇脱氢酶活性,该活性由乙醇特异性诱导。该基因的启动子被用于在乳酸克鲁维酵母中表达异源蛋白,乳酸克鲁维酵母是一种非常有前景的生物体,由于其良好的分泌特性,可作为酿酒酵母的替代宿主。在本文中,我们报道了在KlADH4启动子控制下,细菌β-葡萄糖醛酸酶和人血清白蛋白(HSA)基因在乳酸克鲁维酵母中的乙醇驱动表达。特别是,我们用整合型和复制型载体研究了重组HSA(rHSA)的胞外生产,并用多拷贝载体使该蛋白的产量显著增加,表明细胞中不存在KlADH4反式作用因子的限制。通过对启动子的缺失分析,我们鉴定出一个元件(UASE),它足以被乙醇诱导KlADH4,并且当插入到相应启动子中时,能使其他酵母基因如PGK和LAC4依赖乙醇激活。我们还分析了培养基成分对细胞生长和蛋白质分泌的影响。通过从分批培养(0.3克/升)转变为以乙醇作为首选碳源的补料分批培养(1克/升),重组蛋白的产量有了明显提高。