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巨大芽孢杆菌中编码小酸溶性芽孢蛋白B的基因的克隆及核苷酸序列分析

Cloning and nucleotide sequence of the Bacillus megaterium gene coding for small, acid-soluble spore protein B.

作者信息

Hackett R H, Setlow B, Setlow P

出版信息

J Bacteriol. 1986 Nov;168(2):1023-5. doi: 10.1128/jb.168.2.1023-1025.1986.

Abstract

The Bacillus megaterium gene coding for small, acid-soluble spore protein (SASP) B was cloned and its nucleotide sequence was determined. The amino acid sequence predicted from the DNA sequence was identical to that determined previously for SASP B, with the exception of the amino-terminal methionine predicted from the gene sequence which is presumably removed posttranslationally and an asparagine residue predicted at position 21 which was originally identified as an aspartate residue. The mRNA encoded by the SASP B gene is synthesized for only a discrete period midway in sporulation, in parallel with mRNAs coding for other SASPs. The small size of the SASP B mRNA (365 nucleotides) indicated that the mRNA is monocistronic. The SASP B gene itself hybridized strongly to only one band in Southern blots of restriction enzyme digests of B. megaterium DNA, suggesting that the SASP B gene is not a member of a highly conserved multigene family, as is the case for other SASP genes.

摘要

编码小酸溶性芽孢蛋白(SASP)B的巨大芽孢杆菌基因被克隆,并测定了其核苷酸序列。从DNA序列预测的氨基酸序列与先前确定的SASP B的氨基酸序列相同,但基因序列预测的氨基末端甲硫氨酸可能在翻译后被去除,并且在第21位预测有一个天冬酰胺残基,最初被鉴定为天冬氨酸残基。SASP B基因编码的mRNA仅在芽孢形成中期的一个离散时间段内合成,与编码其他SASP的mRNA同时合成。SASP B mRNA的小尺寸(365个核苷酸)表明该mRNA是单顺反子的。在巨大芽孢杆菌DNA的限制性酶切消化的Southern印迹中,SASP B基因本身仅与一条带强烈杂交,这表明SASP B基因不像其他SASP基因那样是高度保守的多基因家族的成员。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9374/213588/9f76751c1b45/jbacter00204-0564-a.jpg

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