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鲑鱼病原菌鲑肾杆菌57-kDa主要可溶性抗原编码基因的分子克隆与序列分析

Molecular cloning and sequence analysis of the gene coding for the 57-kDa major soluble antigen of the salmonid fish pathogen Renibacterium salmoninarum.

作者信息

Chien M S, Gilbert T L, Huang C, Landolt M L, O'Hara P J, Winton J R

机构信息

School of Fisheries, University of Washington, Seattle 98115.

出版信息

FEMS Microbiol Lett. 1992 Sep 15;75(2-3):259-65. doi: 10.1016/0378-1097(92)90414-j.

Abstract

The complete sequence coding for the 57-kDa major soluble antigen of the salmonid fish pathogen, Renibacterium salmoninarum, was determined. The gene contained an opening reading frame of 1671 nucleotides coding for a protein of 557 amino acids with a calculated M(r) value of 57,190. The first 26 amino acids constituted a signal peptide. The deduced sequence for amino acid residues 27-61 was in agreement with the 35 N-terminal amino acid residues determined by microsequencing, suggesting the protein is synthesized as a 557-amino acid precursor and processed to produce a mature protein of M(r) 54,505. Two regions of the protein contained imperfect direct repeats. The first region contained two copies of an 81-residue repeat, the second contained five copies of an unrelated 25-residue repeat. Also, a perfect inverted repeat (including three in-frame UAA stop codons) was observed at the carboxyl-terminus of the gene.

摘要

已确定鲑鱼致病菌鲑肾杆菌(Renibacterium salmoninarum)57-kDa主要可溶性抗原的完整编码序列。该基因包含一个1671个核苷酸的开放阅读框,编码一个557个氨基酸的蛋白质,计算所得的M(r)值为57,190。前26个氨基酸构成一个信号肽。推导的第27至61位氨基酸残基序列与通过微量测序确定的35个N端氨基酸残基一致,表明该蛋白质作为一个557个氨基酸的前体合成,并经过加工产生一个M(r)为54,505的成熟蛋白质。该蛋白质的两个区域包含不完全直接重复序列。第一个区域包含两个81个残基重复序列的拷贝,第二个区域包含五个不相关的25个残基重复序列的拷贝。此外,在该基因的羧基末端观察到一个完美的反向重复序列(包括三个框内UAA终止密码子)。

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