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首页> 外文期刊>Journal of bacteriology >aarC, an essential gene involved in density-dependent regulation of the 2'-N-acetyltransferase in Providencia stuartii.
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aarC, an essential gene involved in density-dependent regulation of the 2'-N-acetyltransferase in Providencia stuartii.

机译:aarC,一个必需基因,参与斯图亚特氏菌中2'-N-乙酰基转移酶的密度依赖性调节。

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摘要

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.
机译:Providencia stuartii中的2'-N-乙酰基转移酶[AAC(2')-Ia]具有双重功能,其中涉及肽聚糖和某些氨基糖苷的乙酰化。寻找aac(2')-Ia基因的负调控因子已导致aarC的鉴定。错义等位基因(aarC1)从aac(2')-lacZ转录融合物中导致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积累的增加对高密度细胞具有特异性。另外,aarC1等位基因还导致aacP(aac(2')-Ia基因的转录激活因子)的表达大量增加。通过互补分离野生型aarC基因,其编码365个氨基酸的预测蛋白,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图亚特氏菌中的aarC1等位基因。 aarC1等位基因被鉴定为T到G的转化,导致AarC蛋白中第136位的缬氨酸取代为甘氨酸。 aarC基因似乎对细胞生存力至关重要,因为只有在携带aarC或gcpE游离复制的细胞中,才能构建破损的拷贝(aarC :: lacZ)。

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