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编码戊二酸盐辅酶A转移酶的两个基因在发酵氨基酸球菌中羟基戊二酸操纵子起始处的定位。

Location of the two genes encoding glutaconate coenzyme A-transferase at the beginning of the hydroxyglutarate operon in Acidaminococcus fermentans.

作者信息

Mack M, Bendrat K, Zelder O, Eckel E, Linder D, Buckel W

机构信息

Laboratorium für Mikrobiologie des Fachbereichs Biologie, Philipps-Universität Marburg, Germany.

出版信息

Eur J Biochem. 1994 Nov 15;226(1):41-51. doi: 10.1111/j.1432-1033.1994.tb20024.x.

Abstract

Glutaconate coenzyme A-transferase (Gct) from Acidaminococcus fermentans consists of two subunits (GctA, 35725 Da and GctB, 29168 Da). The N-termini sequences of both subunits were determined. DNA sequencing of a subgenomic fragment of A. fermentans revealed that the genes encoding glutaconate CoA-transferase (gctAB) are located upstream of a gene cluster formed by gcdA, hgdC, hgdA and hgdB in this order. Further upstream of gctA, a DNA sequence was detected showing significant similarities to sigma 70-type promoters from Escherichia coli. Primer-extension analysis revealed that this specific DNA sequence was indeed the location of transcription initiation in A. fermentans. The entire gene cluster, 7.3 kb in length, comprising gctAB, gcdA and hgdCAB, has tentatively been named the hydroxyglutarate operon, since the enzymes encoded by these genes are involved in the conversion of (R)-2-hydroxyglutarate to crotonyl-CoA in the pathway of glutamate fermentation by A. fermentans. The genes gctAB were expressed together in E. coli. Cell-free extracts of a transformant E. coli strain contained glutaconate CoA-transferase at a specific activity of up to 30 U/mg protein. The recombinant enzyme was purified to homogeneity with a specific activity of 130 U/mg protein by ammonium sulfate fractionation and crystallisation. The amino acid residue directly involved in catalysis was tentatively identified as E54 of the small subunit of the enzyme (GctB).

摘要

来自发酵氨基酸球菌的戊二酸盐辅酶A转移酶(Gct)由两个亚基组成(GctA,35725道尔顿和GctB,29168道尔顿)。确定了两个亚基的N端序列。对发酵氨基酸球菌亚基因组片段的DNA测序表明,编码戊二酸盐辅酶A转移酶的基因(gctAB)位于由gcdA、hgdC、hgdA和hgdB依次形成的基因簇上游。在gctA的更上游,检测到一个与大肠杆菌σ70型启动子有显著相似性的DNA序列。引物延伸分析表明,这个特定的DNA序列确实是发酵氨基酸球菌转录起始的位置。整个基因簇长度为7.3 kb,包括gctAB、gcdA和hgdCAB,由于这些基因编码的酶参与了发酵氨基酸球菌在谷氨酸发酵途径中将(R)-2-羟基戊二酸转化为巴豆酰辅酶A的过程,因此暂时被命名为羟基戊二酸操纵子。gctAB基因在大肠杆菌中共同表达。转化后的大肠杆菌菌株的无细胞提取物中含有戊二酸盐辅酶A转移酶,比活性高达30 U/mg蛋白。通过硫酸铵分级分离和结晶,将重组酶纯化至同质,比活性为130 U/mg蛋白。初步确定直接参与催化的氨基酸残基为该酶小亚基(GctB)的E54。

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