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大肠杆菌 D-丝氨酸转运及耐药突变体的特性研究。

Characterization of Escherichia coli D-cycloserine transport and resistant mutants.

机构信息

Department of Medical Microbiology & Immunology and Department of Biochemistry, University of Wisconsin, Madison, WI, USA.

出版信息

J Bacteriol. 2013 Apr;195(7):1389-99. doi: 10.1128/JB.01598-12. Epub 2013 Jan 11.

Abstract

d-Cycloserine (DCS) is a broad-spectrum antibiotic that inhibits d-alanine ligase and alanine racemase activity. When Escherichia coli K-12 or CFT073 is grown in minimal glucose or glycerol medium, CycA transports DCS into the cell. E. coli K-12 cycA and CFT073 cycA mutant strains display increased DCS resistance when grown in minimal medium. However, the cycA mutants exhibit no change in DCS sensitivity compared to their parental strains when grown in LB (CFT073 and K-12) or human urine (CFT073 only). These data suggest that cycA does not participate in DCS sensitivity when strains are grown in a non-minimal medium. The small RNA GvcB acts as a negative regulator of E. coli K-12 cycA expression when grown in LB. Three E. coli K-12 gcvB mutant strains failed to demonstrate a change in DCS sensitivity when grown in LB. This further suggests a limited role for cycA in DCS sensitivity. To aid in the identification of E. coli genes involved in DCS sensitivity when grown on complex media, the Keio K-12 mutant collection was screened for DCS-resistant strains. dadA, pnp, ubiE, ubiF, ubiG, ubiH, and ubiX mutant strains showed elevated DCS resistance. The phenotypes associated with these mutants were used to further define three previously characterized E. coli DCS-resistant strains (χ316, χ444, and χ453) isolated by Curtiss and colleagues (R. Curtiss, III, L. J. Charamella, C. M. Berg, and P. E. Harris, J. Bacteriol. 90:1238-1250, 1965). A dadA mutation was identified in both χ444 and χ453. In addition, results are presented that indicate for the first time that DCS can antagonize d-amino acid dehydrogenase (DadA) activity.

摘要

d-环丝氨酸(DCS)是一种广谱抗生素,可抑制 d-丙氨酸连接酶和丙氨酸消旋酶的活性。当大肠杆菌 K-12 或 CFT073 在最小葡萄糖或甘油培养基中生长时,CycA 将 DCS 运入细胞。当在最小培养基中生长时,大肠杆菌 K-12 cycA 和 CFT073 cycA 突变株对 DCS 的抗性增加。然而,与亲本菌株相比,cycA 突变株在 LB(CFT073 和 K-12)或人尿(仅 CFT073)中生长时,对 DCS 的敏感性没有变化。这些数据表明,当菌株在非最小培养基中生长时,cycA 不参与 DCS 敏感性。当在 LB 中生长时,小 RNA GvcB 作为大肠杆菌 K-12 cycA 表达的负调节剂。三种大肠杆菌 K-12 gcvB 突变株在 LB 中生长时,DCS 敏感性没有变化。这进一步表明 cycA 在 DCS 敏感性中的作用有限。为了帮助鉴定在复杂培养基上生长时涉及 DCS 敏感性的大肠杆菌基因,对 Keio K-12 突变体文库进行了筛选,以寻找 DCS 抗性菌株。dadA、pnp、ubiE、ubiF、ubiG、ubiH 和 ubiX 突变株显示出较高的 DCS 抗性。与这些突变体相关的表型被进一步用于定义由 Curtiss 及其同事(R. Curtiss,III,L. J. Charamella,C. M. Berg 和 P. E. Harris,J. Bacteriol. 90:1238-1250,1965)分离的三种先前表征的大肠杆菌 DCS 抗性菌株(χ316、χ444 和 χ453)。在 χ444 和 χ453 中均发现了 dadA 突变。此外,结果表明,DCS 可以首次拮抗 d-氨基酸脱氢酶(DadA)活性。

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