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Proteomics-based confirmation of protein expression and correction of annotation errors in the Brucella abortus genome.基于蛋白质组学的布鲁氏菌 abortus 基因组中蛋白质表达的确认和注释错误的修正。
BMC Genomics. 2010 May 12;11:300. doi: 10.1186/1471-2164-11-300.
2
Bacillus subtilis GlcK activity requires cysteines within a motif that discriminates microbial glucokinases into two lineages.枯草芽孢杆菌葡萄糖激酶(GlcK)的活性需要一个基序内的半胱氨酸,该基序可将微生物葡萄糖激酶分为两个谱系。
BMC Microbiol. 2004 Feb 3;4:6. doi: 10.1186/1471-2180-4-6.
3
Molecular characterization of glucokinase from Escherichia coli K-12.来自大肠杆菌K-12的葡萄糖激酶的分子特征
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本文引用的文献

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THE UTILIZATION OF GLUCOSE 6-PHOSPHATE BY GLUCOKINASELESS AND WILD-TYPE STRAINS OF ESCHERICHIA COLI.葡萄糖激酶缺陷型和野生型大肠杆菌菌株对6-磷酸葡萄糖的利用情况
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Hybridization between Escherichia coli and Shigella.大肠杆菌与志贺氏菌之间的杂交。
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Cloning of genes for proline and leucine biosynthesis from Brucella abortus by functional complementation in Escherichia coli.通过在大肠杆菌中进行功能互补从流产布鲁氏菌克隆脯氨酸和亮氨酸生物合成基因。
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ABC transporters: bacterial exporters.ABC转运蛋白:细菌外排泵
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Distantly related sequences in the alpha- and beta-subunits of ATP synthase, myosin, kinases and other ATP-requiring enzymes and a common nucleotide binding fold.ATP合酶、肌球蛋白、激酶及其他需ATP的酶的α亚基和β亚基中关系较远的序列以及一个共同的核苷酸结合结构域。
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Identification of the uvrA gene product.uvrA基因产物的鉴定。
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7
Construction of an Hfr strain useful for transferring recA mutations between Escherichia coli strains.构建一种有助于在大肠杆菌菌株之间转移recA突变的高频重组(Hfr)菌株。
J Bacteriol. 1980 Jul;143(1):529-30. doi: 10.1128/jb.143.1.529-530.1980.
8
Glucose transport in Brucella abortus.布鲁氏菌流产亚种中的葡萄糖转运
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9
Cloning of genes specifying carbohydrate catabolism in Pseudomonas aeruginosa and Pseudomonas putida.铜绿假单胞菌和恶臭假单胞菌中负责碳水化合物分解代谢的基因克隆。
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10
Sequence and genetic organization of a Zymomonas mobilis gene cluster that encodes several enzymes of glucose metabolism.运动发酵单胞菌中一个编码葡萄糖代谢多种酶的基因簇的序列和遗传组织。
J Bacteriol. 1990 Dec;172(12):7227-40. doi: 10.1128/jb.172.12.7227-7240.1990.

流产布鲁氏菌19型葡萄糖激酶基因的克隆、特性分析及其他三个基因的鉴定

Cloning and characterization of the glucokinase gene of Brucella abortus 19 and identification of three other genes.

作者信息

Essenberg R C

机构信息

Department of Biochemistry, Oklahoma State University, Stillwater 74078, USA.

出版信息

J Bacteriol. 1995 Nov;177(21):6297-300. doi: 10.1128/jb.177.21.6297-6300.1995.

DOI:10.1128/jb.177.21.6297-6300.1995
PMID:7592399
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC177474/
Abstract

A clone from Brucella abortus 19 complemented an Escherichia coli strain deficient in phosphorylation of glucose. Open reading frames similar to E. coli mepA, glk, and genes encoding ATP-coupled exporters were found in the sequence. A fourth affected growth on minimal media of the ptsI glk strain with various carbon sources.

摘要

来自流产布鲁氏菌19的一个克隆补充了一株葡萄糖磷酸化缺陷的大肠杆菌菌株。在该序列中发现了与大肠杆菌mepA、glk相似的开放阅读框以及编码ATP偶联转运蛋白的基因。第四个基因影响了ptsI glk菌株在含有各种碳源的基本培养基上的生长。