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米曲霉碱性蛋白酶的全长cDNA克隆:结构分析及在酿酒酵母中的表达

A full length cDNA clone for the alkaline protease from Aspergillus oryzae: structural analysis and expression in Saccharomyces cerevisiae.

作者信息

Tatsumi H, Ogawa Y, Murakami S, Ishida Y, Murakami K, Masaki A, Kawabe H, Arimura H, Nakano E, Motai H

机构信息

Research and Development Division, Kikkoman Corporation, Chiba, Japan.

出版信息

Mol Gen Genet. 1989 Oct;219(1-2):33-8. doi: 10.1007/BF00261154.

Abstract

We have cloned and determined the nucleotide sequence of a cDNA fragment for the entire coding region of the alkaline protease (Alp) from a filamentous ascomycete Aspergillus oryzae. According to the deduced amino acid sequence, Alp has a putative prepro region of 121 amino acids preceding the mature region, which consists of 282 amino acids. A consensus sequence of a signal peptide consisting of 21 amino acids is found at the N-terminus of the prepro region. The primary structure of the mature region shares extensive homology (29%-44%) with those of subtilisin families, and the three residues (Asp 32, His 64 and Ser 221 in subtilisin BPN') composing the active site are preserved. The entire cDNA, coding for prepro Alp, when introduced into the yeast Saccharomyces cerevisiae, directed the secretion of enzymatically active Alp into the culture medium, with its N-terminus and specific activity identical to native Aspergillus Alp.

摘要

我们已经克隆并测定了来自丝状子囊菌米曲霉的碱性蛋白酶(Alp)整个编码区的cDNA片段的核苷酸序列。根据推导的氨基酸序列,Alp在由282个氨基酸组成的成熟区之前有一个121个氨基酸的推定前原区。在前原区的N端发现了一个由21个氨基酸组成的信号肽共有序列。成熟区的一级结构与枯草杆菌蛋白酶家族的结构具有广泛的同源性(29%-44%),并且构成活性位点的三个残基(枯草杆菌蛋白酶BPN'中的Asp 32、His 64和Ser 221)得以保留。编码前原Alp的完整cDNA导入酵母酿酒酵母后,可将具有酶活性的Alp分泌到培养基中,其N端和比活性与天然米曲霉Alp相同。

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