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肺炎链球菌Era GTP酶C末端部分与16S rRNA和细胞质膜相互作用的分析

Analysis of the interaction of 16S rRNA and cytoplasmic membrane with the C-terminal part of the Streptococcus pneumoniae Era GTPase.

作者信息

Hang J Q, Meier T I, Zhao G

机构信息

Infectious Diseases Research, Lilly Research Laboratories, Eli Lilly and Company, Indianapolis, IN 46285-0428, USA.

出版信息

Eur J Biochem. 2001 Nov;268(21):5570-7. doi: 10.1046/j.1432-1033.2001.02493.x.

Abstract

Era, an essential GTPase, plays a regulatory role in several cellular processes. The Era protein of Streptococcus pneumoniae has recently been shown to bind to 16S rRNA and the cytoplasmic membrane. However, exact locations of Era responsible for RNA- and membrane-binding were unknown. To identify the regions in Era that interact with the RNA and membrane, the C-terminal part of S. pneumoniae Era was systematically deleted while the N-terminal part, responsible for the GTPase activity of the protein, was kept intact. The resulting truncated Era proteins were purified and characterized. The C-terminal deletion of 9 or 19 amino-acid residues did not affect 16S rRNA-binding activity while further deletions of the C-terminus (29-114 amino-acid residues) abolished the activity. These results indicate that the integrity of the putative KH domain of Era, spanning the amino-acid residues between approximately 22-83 from the C-terminus, is required for 16S rRNA-binding. Furthermore, the Era proteins with a deletion up to 45 residues from the C-terminus retained membrane-binding activity, but longer deletions significantly reduced the activity. These results indicate that part of the putative KH domain is also required for membrane-binding. Thus, these results indicate for the first time that the regions critical for the membrane- and 16S rRNA-binding activities of Era overlap. The era gene with a deletion of 9 or 19 codons from its 3' terminus complemented an Escherichia coli mutant strain deficient in Era production whereas the genes with longer deletions failed to do so, thereby indicating that the KH domain is essential for Era function. Taken together, the results of this study indicate that the putative KH domain is required for 16S rRNA-binding activity and that part of the KH domain is also required for membrane-binding activity. The results also suggest that the interaction between Era and 16S rRNA is essential for bacterial growth.

摘要

Era是一种必需的GTP酶,在多个细胞过程中发挥调节作用。最近发现肺炎链球菌的Era蛋白可与16S rRNA和细胞质膜结合。然而,Era中负责RNA结合和膜结合的确切位置尚不清楚。为了确定Era中与RNA和膜相互作用的区域,系统地删除了肺炎链球菌Era的C末端部分,而负责该蛋白GTP酶活性的N末端部分保持完整。对得到的截短Era蛋白进行了纯化和表征。C末端缺失9或19个氨基酸残基不影响16S rRNA结合活性,而C末端的进一步缺失(29 - 114个氨基酸残基)则消除了该活性。这些结果表明,Era假定的KH结构域的完整性(从C末端起约22 - 83个氨基酸残基之间)是16S rRNA结合所必需的。此外,C末端缺失多达45个残基的Era蛋白仍保留膜结合活性,但更长的缺失会显著降低该活性。这些结果表明,假定的KH结构域的一部分也是膜结合所必需的。因此,这些结果首次表明,Era中对膜结合和16S rRNA结合活性至关重要的区域相互重叠。从其3'末端缺失9或19个密码子的era基因可互补缺乏Era产生的大肠杆菌突变菌株,而缺失更长的基因则不能,从而表明KH结构域对Era功能至关重要。综上所述,本研究结果表明假定的KH结构域是16S rRNA结合活性所必需的,且KH结构域的一部分也是膜结合活性所必需的。结果还表明Era与16S rRNA之间的相互作用对细菌生长至关重要。

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