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大肠杆菌核糖核酸酶D:rnd结构基因的测序及过表达蛋白的纯化

Escherichia coli RNase D: sequencing of the rnd structural gene and purification of the overexpressed protein.

作者信息

Zhang J R, Deutscher M P

机构信息

Department of Biochemistry, University of Connecticut Health Center, Farmington 06032.

出版信息

Nucleic Acids Res. 1988 Jul 25;16(14A):6265-78. doi: 10.1093/nar/16.14.6265.

Abstract

We have determined the nucleotide sequence of a 1.4-kb-pair fragment of the E. coli chromosome that carries the complete rnd gene encoding RNase D, a putative tRNA processing enzyme. The coding region of rnd extends for a total of 1128 nucleotides beginning at an initiator UUG codon and terminating at a UAA codon, and encodes a 375-amino acid polypeptide of 42,679 daltons, consistent with the known size of RNase D. A rapid purification procedure was developed for isolation of RNase D from strains overexpressing the enzyme. The N-terminal sequence and the amino acid composition of the homogenous protein were in excellent agreement with those derived from the sequence of the rnd gene.

摘要

我们已经确定了大肠杆菌染色体上一个1.4千碱基对片段的核苷酸序列,该片段携带编码RNase D(一种假定的tRNA加工酶)的完整rnd基因。rnd的编码区域从起始UUG密码子开始,到UAA密码子结束,全长共1128个核苷酸,编码一个由375个氨基酸组成、分子量为42,679道尔顿的多肽,这与已知的RNase D大小相符。我们开发了一种快速纯化程序,用于从过量表达该酶的菌株中分离RNase D。该纯化蛋白的N端序列和氨基酸组成与从rnd基因序列推导出来的结果高度一致。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/81fb/338294/f7d593c9c4a4/nar00167-0022-a.jpg

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