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aarC,一个参与斯氏普罗威登斯菌中2'-N-乙酰转移酶密度依赖性调控的必需基因。

aarC, an essential gene involved in density-dependent regulation of the 2'-N-acetyltransferase in Providencia stuartii.

作者信息

Rather P N, Solinsky K A, Paradise M R, Parojcic M M

机构信息

Department of Medicine, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.

出版信息

J Bacteriol. 1997 Apr;179(7):2267-73. doi: 10.1128/jb.179.7.2267-2273.1997.

Abstract

The 2'-N-acetyltransferase [AAC(2')-Ia] in Providencia stuartii has a dual function where it is involved in the acetylation of peptidoglycan and certain aminoglycosides. A search for negative regulators of the aac(2')-Ia gene has resulted in the identification of aarC. A missense allele (aarC1) resulted in an 8.9-fold increase in beta-galactosidase accumulation from an aac(2')-lacZ transcriptional fusion. Northern blot analysis demonstrated an increase in aac(2')-Ia mRNA accumulation that was specific to cells at high density. In addition, the aarC1 allele also resulted in a substantial increase in the expression of aarP, a transcriptional activator of the aac(2')-Ia gene. The wild-type aarC gene was isolated by complementation and encodes a predicted protein of 365 amino acids with a molecular mass of 39,815 Da. The predicted AarC protein exhibited 88% amino acid homology to the previously identified GcpE protein of Escherichia coli and 86% homology to a gene product from Haemophilus influenzae. The E. coli gcpE gene was able to functionally complement the aarC1 allele in P. stuartii. The aarC1 allele was identified as a T to G transversion that resulted in a valine to glycine substitution at position 136 in the AarC protein. The aarC gene appears to be essential for cell viability as construction of a disrupted copy (aarC::lacZ) was possible only in cells that carried an episomal copy of aarC or gcpE.

摘要

斯氏普罗威登斯菌中的2'-N-乙酰基转移酶[AAC(2')-Ia]具有双重功能,它参与肽聚糖和某些氨基糖苷类的乙酰化作用。对aac(2')-Ia基因的负调控因子进行搜索,结果鉴定出了aarC。一个错义等位基因(aarC1)导致来自aac(2')-lacZ转录融合体的β-半乳糖苷酶积累增加了8.9倍。Northern印迹分析表明,aac(2')-Ia mRNA积累增加,这在高密度细胞中具有特异性。此外,aarC1等位基因还导致aac(2')-Ia基因的转录激活因子aarP的表达大幅增加。野生型aarC基因通过互补作用分离得到,编码一个预测的365个氨基酸的蛋白质,分子量为39,815 Da。预测的AarC蛋白与先前鉴定的大肠杆菌GcpE蛋白具有88%的氨基酸同源性,与流感嗜血杆菌的一个基因产物具有86%的同源性。大肠杆菌gcpE基因能够在功能上互补斯氏普罗威登斯菌中的aarC1等位基因。aarC1等位基因被鉴定为一个T到G的颠换,导致AarC蛋白第136位的缬氨酸被甘氨酸取代。aarC基因似乎对细胞活力至关重要,因为只有在携带aarC或gcpE附加体拷贝的细胞中才可能构建缺失拷贝(aarC::lacZ)。

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