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1
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J Bacteriol. 1995 Jul;177(13):3885-9. doi: 10.1128/jb.177.13.3885-3889.1995.
2
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3
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8
Sequence analysis of the Pseudomonas sp. strain P51 tcb gene cluster, which encodes metabolism of chlorinated catechols: evidence for specialization of catechol 1,2-dioxygenases for chlorinated substrates.编码氯代儿茶酚代谢的假单胞菌属菌株P51的tcb基因簇的序列分析:儿茶酚1,2-双加氧酶对氯代底物特异性的证据
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Genuine genetic redundancy in maleylacetate-reductase-encoding genes involved in degradation of haloaromatic compounds by Cupriavidus necator JMP134.涉及贪铜菌JMP134对卤代芳香化合物降解的马来酰乙酸还原酶编码基因中的真正遗传冗余。
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本文引用的文献

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Conversion of 2-chloromaleylacetate in Alcaligenes eutrophus JMP134.食碱假单胞菌JMP134中2-氯马来酰乙酸的转化
Arch Microbiol. 1993;159(2):182-8. doi: 10.1007/BF00250280.
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Nucleotide sequence and initial functional characterization of the clcR gene encoding a LysR family activator of the clcABD chlorocatechol operon in Pseudomonas putida.恶臭假单胞菌中编码clcABD氯儿茶酚操纵子的LysR家族激活因子的clcR基因的核苷酸序列及初步功能表征
J Bacteriol. 1993 Jan;175(2):417-27. doi: 10.1128/jb.175.2.417-427.1993.
3
Degradation of chloroaromatics: purification and characterization of maleylacetate reductase from Pseudomonas sp. strain B13.氯代芳烃的降解:来自假单胞菌属B13菌株的马来酰乙酸还原酶的纯化与表征
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Purification and characterization of maleylacetate reductase from Alcaligenes eutrophus JMP134(pJP4).从嗜碱假单胞菌JMP134(pJP4)中纯化和鉴定马来酸乙酸还原酶
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Analysis of duplicated gene sequences associated with tfdR and tfdS in Alcaligenes eutrophus JMP134.嗜碱假单胞菌JMP134中与tfdR和tfdS相关的重复基因序列分析。
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Maleylacetate reductase of Pseudomonas sp. strain B13: specificity of substrate conversion and halide elimination.假单胞菌属B13菌株的马来酰乙酸还原酶:底物转化特异性和卤化物消除
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7
Evolution of chlorocatechol catabolic pathways. Conclusions to be drawn from comparisons of lactone hydrolases.氯代儿茶酚分解代谢途径的演变。从内酯水解酶比较中得出的结论。
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Sequence analysis of a gene cluster involved in metabolism of 2,4,5-trichlorophenoxyacetic acid by Burkholderia cepacia AC1100.洋葱伯克霍尔德菌AC1100中参与2,4,5-三氯苯氧乙酸代谢的基因簇的序列分析
Appl Environ Microbiol. 1995 Apr;61(4):1279-89. doi: 10.1128/aem.61.4.1279-1289.1995.
9
Plasmid specifying total degradation of 3-chlorobenzoate by a modified ortho pathway.通过改良的邻位途径实现3-氯苯甲酸完全降解的质粒。
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10
Restriction mapping of a chlorobenzoate degradative plasmid and molecular cloning of the degradative genes.氯苯甲酸酯降解性质粒的限制酶切图谱分析及降解基因的分子克隆
Gene. 1984 Feb;27(2):173-81. doi: 10.1016/0378-1119(84)90138-0.

操纵子tcb、tfd和clc编码马来酰乙酸还原酶(改良邻位途径的第四种酶)的证据。

Evidence that operons tcb, tfd, and clc encode maleylacetate reductase, the fourth enzyme of the modified ortho pathway.

作者信息

Kasberg T, Daubaras D L, Chakrabarty A M, Kinzelt D, Reineke W

机构信息

Bergische Universität-Gesamthochschule Wuppertal, Germany.

出版信息

J Bacteriol. 1995 Jul;177(13):3885-9. doi: 10.1128/jb.177.13.3885-3889.1995.

DOI:10.1128/jb.177.13.3885-3889.1995
PMID:7601858
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177112/
Abstract

The maleylacetate reductase from Pseudomonas sp. strain B13 functioning in the modified ortho pathway was purified and digested with trypsin. The polypeptides separated by high-performance liquid chromatography were sequenced. Alignments with the polypeptides predicted from the tfdF and tcbF genes located on plasmids pJP4 of the 2,4-dichlorophenoxyacetate-degrading Alcaligenes eutrophus JMP134 and pP51 of the 1,2,4-trichlorobenzene-degrading Pseudomonas sp. strain P51 as well as polypeptides predicted from the tftE gene located on the chromosome of the 2,4,5-trichlorophenoxyacetate-degrading Burkholderia cepacia AC1100 were obtained. In addition, the deduced protein sequence encoded by the nucleotide sequence downstream of clcD on plasmid pAC27 of the 3-chlorobenzoate-degrading Pseudomonas putida AC866 was tested for homology. Significant sequence similarities with the polypeptides encoded by the tfdF, tcbF, and tftE genes as well as the nucleotide sequence downstream of the clcD gene gave evidence that these genes might encode maleylacetate reductases. A NAD-binding motif in a beta alpha beta-element was detected.

摘要

对在改良邻位途径中发挥作用的来自假单胞菌属菌株B13的马来酰乙酸还原酶进行了纯化,并用胰蛋白酶消化。对通过高效液相色谱分离的多肽进行了测序。获得了与从降解2,4-二氯苯氧基乙酸的真养产碱菌JMP134的质粒pJP4上的tfdF和tcbF基因以及降解1,2,4-三氯苯的假单胞菌属菌株P51的质粒pP51上预测的多肽的比对结果,以及与从降解2,4,5-三氯苯氧基乙酸的洋葱伯克霍尔德菌AC1100染色体上的tftE基因预测的多肽的比对结果。此外,还对3-氯苯甲酸降解菌恶臭假单胞菌AC866的质粒pAC27上clcD下游核苷酸序列编码的推导蛋白质序列进行了同源性测试。与tfdF、tcbF和tftE基因编码的多肽以及clcD基因下游核苷酸序列的显著序列相似性表明,这些基因可能编码马来酰乙酸还原酶。在一个β-α-β元件中检测到一个NAD结合基序。