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大肠杆菌K12中具有反馈抗性N-乙酰谷氨酸合酶突变体的分离与鉴定。

Isolation and characterization of mutants with a feedback resistant N-acetylglutamate synthase in Escherichia coli K 12.

作者信息

Eckhardt T, Leisinger T

出版信息

Mol Gen Genet. 1975 Jun 19;138(3):225-32. doi: 10.1007/BF00269349.

DOI:10.1007/BF00269349
PMID:1102931
Abstract

Mutants with a feedback resistant N-acetylglutamate synthase have been isolated from a proA/B, argD, argR strain by screening for proline excretion on minimal medium with arginine. The feedback resistant character of three mutants was transduced into an argA (N-acetylglutamate synthase negative) strain. It was cotransducible with argA at a frequency of greater than 99%. N-acetylglutamate synthase extracted from the three mutants was approximately one hundred times less sensitive to L-arginine than the enzyme from the feedback sensitive parent strain.

摘要

通过在含有精氨酸的基本培养基上筛选脯氨酸排泄情况,从proA/B、argD、argR菌株中分离出了具有反馈抗性的N-乙酰谷氨酸合酶突变体。三个突变体的反馈抗性特征被转导到argA(N-乙酰谷氨酸合酶阴性)菌株中。它与argA的共转导频率大于99%。从这三个突变体中提取的N-乙酰谷氨酸合酶对L-精氨酸的敏感性比来自反馈敏感亲本菌株的酶低约一百倍。

相似文献

1
Isolation and characterization of mutants with a feedback resistant N-acetylglutamate synthase in Escherichia coli K 12.大肠杆菌K12中具有反馈抗性N-乙酰谷氨酸合酶突变体的分离与鉴定。
Mol Gen Genet. 1975 Jun 19;138(3):225-32. doi: 10.1007/BF00269349.
2
Expression of the argA gene carried by a defective lambda bacteriophage of Escherichia coli.由大肠杆菌的缺陷型λ噬菌体携带的argA基因的表达。
J Bacteriol. 1976 Mar;125(3):1217-9. doi: 10.1128/jb.125.3.1217-1219.1976.
3
Use of inducible feedback-resistant N-acetylglutamate synthetase (argA) genes for enhanced arginine biosynthesis by genetically engineered Escherichia coli K-12 strains.利用可诱导的抗反馈N-乙酰谷氨酸合成酶(argA)基因通过基因工程改造的大肠杆菌K-12菌株增强精氨酸生物合成
Appl Environ Microbiol. 1998 May;64(5):1805-11. doi: 10.1128/AEM.64.5.1805-1811.1998.
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Construction of an L-arginine-producing mutant in Serratia marcescens. Use of the wide substrate specificity of acetylornithinase.粘质沙雷氏菌中L-精氨酸生产突变体的构建。乙酰鸟氨酸酶广泛底物特异性的应用。
J Biochem. 1978 Oct;84(4):881-90. doi: 10.1093/oxfordjournals.jbchem.a132200.
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The genetic organization of arginine biosynthesis in Pseudomonas aeruginosa.铜绿假单胞菌中精氨酸生物合成的基因组织。
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Proline excretion and indirect suppression in Escherichia coli and Salmonella typhimurium.大肠杆菌和鼠伤寒沙门氏菌中的脯氨酸排泄与间接抑制作用。
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Evidence in vitro for a participation of the arginine repressor in cumulative repression of Escherichia coli carbamoylphosphate synthase [proceedings].体外证据表明精氨酸阻遏物参与大肠杆菌氨甲酰磷酸合酶的累积阻遏作用[会议论文集]
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引用本文的文献

1
Use of inducible feedback-resistant N-acetylglutamate synthetase (argA) genes for enhanced arginine biosynthesis by genetically engineered Escherichia coli K-12 strains.利用可诱导的抗反馈N-乙酰谷氨酸合成酶(argA)基因通过基因工程改造的大肠杆菌K-12菌株增强精氨酸生物合成
Appl Environ Microbiol. 1998 May;64(5):1805-11. doi: 10.1128/AEM.64.5.1805-1811.1998.
2
Isolation of plasmids carrying the arginine repressor gene argR of Escherichia coli K12.携带大肠杆菌K12精氨酸阻遏基因argR的质粒的分离。
Mol Gen Genet. 1980;178(2):447-52. doi: 10.1007/BF00270498.
3
Regulation of argA operon expression in Escherichia coli K-12: cell-free synthesis of beta-galactosidase under argA control.

本文引用的文献

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Mutants of Escherichia coli requiring methionine or vitamin B12.需要甲硫氨酸或维生素B12的大肠杆菌突变体。
J Bacteriol. 1950 Jul;60(1):17-28. doi: 10.1128/jb.60.1.17-28.1950.
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Feedback inhibition of acetylglutamate synthetase by arginine in Escherichia coli.精氨酸对大肠杆菌中乙酰谷氨酸合成酶的反馈抑制作用。
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A structural gene mutation in Salmonella typhimurium resulting in repressibility of adenylosuccinase.鼠伤寒沙门氏菌中的一种结构基因突变,导致腺苷酸琥珀酸酶的可阻遏性。
Proc Natl Acad Sci U S A. 1965 Oct;54(4):1254-61. doi: 10.1073/pnas.54.4.1254.
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Distribution and function of genes concerned with aromatic biosynthesis in Escherichia coli.大肠杆菌中与芳香族生物合成相关基因的分布与功能
J Bacteriol. 1966 Apr;91(4):1494-508. doi: 10.1128/jb.91.4.1494-1508.1966.
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Current linkage map of Escherichia coli.大肠杆菌当前的连锁图谱。
Bacteriol Rev. 1970 Jun;34(2):155-75. doi: 10.1128/br.34.2.155-175.1970.
10
Acetylhistidine as substrate for acetylornithinase: a new system for the selection of arginine regulation mutants in Escherichia coli.乙酰组氨酸作为乙酰鸟氨酸酶的底物:一种用于筛选大肠杆菌中精氨酸调控突变体的新系统。
Mol Gen Genet. 1970;106(2):162-73. doi: 10.1007/BF00323835.