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Biotechnol Bioeng. 1996 Mar 20;49(6):667-74. doi: 10.1002/(SICI)1097-0290(19960320)49:6<667::AID-BIT8>3.0.CO;2-M.
2
Stable Expression of hom-1-thrB in Corynebacterium glutamicum and Its Effect on the Carbon Flux to Threonine and Related Amino Acids.在谷氨酸棒杆菌中稳定表达 hom-1-thrB 及其对苏氨酸和相关氨基酸碳通量的影响。
Appl Environ Microbiol. 1994 Jan;60(1):126-32. doi: 10.1128/aem.60.1.126-132.1994.
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Exploring the metabolic and genetic control of gene expression on a genomic scale.在基因组规模上探索基因表达的代谢和遗传控制。
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Stress response of yeast.酵母的应激反应。
Biochem J. 1993 Feb 15;290 ( Pt 1)(Pt 1):1-13. doi: 10.1042/bj2900001.
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A Saccharomyces cerevisiae UAS element controlled by protein kinase A activates transcription in response to a variety of stress conditions.由蛋白激酶A控制的酿酒酵母上游激活序列(UAS)元件在多种应激条件下激活转录。
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Curr Genet. 1993 Dec;24(6):465-71. doi: 10.1007/BF00351707.
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Multiple mechanisms provide rapid and stringent glucose repression of GAL gene expression in Saccharomyces cerevisiae.多种机制可对酿酒酵母中GAL基因的表达进行快速且严格的葡萄糖抑制。
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Occurrence of a catabolic L-serine (L-threonine) deaminase in Saccharomyces cerevisiae.酿酒酵母中分解代谢型L-丝氨酸(L-苏氨酸)脱氨酶的存在。
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Genetic and biochemical study of threonine-overproducing mutants of Saccharomyces cerevisiae.酿酒酵母苏氨酸高产突变体的遗传与生化研究。
Mol Cell Biol. 1982 Jul;2(7):731-6. doi: 10.1128/mcb.2.7.731-736.1982.
10
Different base/base mismatches are corrected with different efficiencies by the methyl-directed DNA mismatch-repair system of E. coli.大肠杆菌的甲基化导向DNA错配修复系统对不同的碱基/碱基错配进行校正的效率不同。
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在不同诱导型启动子控制下携带HOM3-R2突变等位基因的酵母菌株中苏氨酸的过量生产。

Threonine overproduction in yeast strains carrying the HOM3-R2 mutant allele under the control of different inducible promoters.

作者信息

Farfán M J, Aparicio L, Calderón I L

机构信息

Departamento de Genética, Facultad de Biología, Universidad de Sevilla, E-41080 Seville, Spain.

出版信息

Appl Environ Microbiol. 1999 Jan;65(1):110-6. doi: 10.1128/AEM.65.1.110-116.1999.

DOI:10.1128/AEM.65.1.110-116.1999
PMID:9872767
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC90990/
Abstract

The HOM3 gene of Saccharomyces cerevisiae codes for aspartate kinase, which plays a crucial role in the regulation of the metabolic flux that leads to threonine biosynthesis. With the aim of obtaining yeast strains able to overproduce threonine in a controlled way, we have placed the HOM3-R2 mutant allele, which causes expression of a feedback-insensitive enzyme, under the control of four distinctive regulatable yeast promoters, namely, PGAL1, PCHA1, PCYC1-HSE2, and PGPH1. The amino acid contents of strains bearing the different constructs were analyzed both under repression and induction conditions. Although some differences in overall threonine production were found, a maximum of around 400 nmol/mg (dry weight) was observed. Other factors, such as excretion to the medium and activity of the catabolic threonine/serine deaminase, also affect threonine accumulation. Thus, improvement of threonine productivity by yeast cells would probably require manipulation of these and other factors.

摘要

酿酒酵母的HOM3基因编码天冬氨酸激酶,该酶在调节导致苏氨酸生物合成的代谢通量中起关键作用。为了获得能够以可控方式过量生产苏氨酸的酵母菌株,我们将导致表达反馈不敏感酶的HOM3-R2突变等位基因置于四个不同的可调控酵母启动子的控制之下,这四个启动子分别是PGAL1、PCHA1、PCYC1-HSE2和PGPH1。在阻遏和诱导条件下,对携带不同构建体的菌株的氨基酸含量进行了分析。虽然在苏氨酸的总体产量上发现了一些差异,但观察到的最大值约为400 nmol/mg(干重)。其他因素,如向培养基中的排泄以及分解代谢型苏氨酸/丝氨酸脱氨酶的活性,也会影响苏氨酸的积累。因此,酵母细胞提高苏氨酸生产力可能需要对这些及其他因素进行调控。