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酿酒酵母MNN9基因的多形汉逊酵母同源物的克隆与特性分析

Cloning and characterization of the Hansenula polymorpha homologue of the Saccharomyces cerevisiae MNN9 gene.

作者信息

Kim S Y, Sohn J H, Kang H A, Yoo S K, Pyun Y R, Choi E S

机构信息

Division of Life Sciences, Korea Research Institute of Bioscience and Biotechnology, Taejon 305-333, Korea.

出版信息

Yeast. 2001 Mar 30;18(5):455-61. doi: 10.1002/yea.699.

Abstract

A gene homologous to Saccharomyces cerevisiae MNN9 has been cloned and characterized in the methylotrophic yeast Hansenula polymorpha. This gene was cloned from a H. polymorpha genomic DNA library using the S. cerevisiae MNN9 gene as a probe. The H. polymorpha MNN9 homologue (HpMNN9) contained a 1062 bp open reading frame encoding a predicted protein of 354 amino acids. The deduced amino acid sequence showed 58% and 51% identity, respectively, with the S. cerevisiae and Candida albicans Mnn9 proteins. Disruption of HpMNN9 leads to phenotypic effects suggestive of cell wall defects, including detergent sensitivity and hygromycin B sensitivity. The hygromycin B sensitivity of S. cerevisiae mnn9 null mutant was complemented in the presence of the HpMNN9 gene. The DNA sequence of the H. polymorpha homologue has been submitted to GenBank with the Accession No. AF264786.

摘要

在多形汉逊酵母中已克隆并鉴定出一个与酿酒酵母MNN9同源的基因。该基因是利用酿酒酵母MNN9基因作为探针,从多形汉逊酵母基因组DNA文库中克隆得到的。多形汉逊酵母MNN9同源物(HpMNN9)含有一个1062 bp的开放阅读框,编码一个预测的354个氨基酸的蛋白质。推导的氨基酸序列与酿酒酵母和白色念珠菌的Mnn9蛋白分别具有58%和51%的同一性。HpMNN9的破坏导致了提示细胞壁缺陷的表型效应,包括去污剂敏感性和潮霉素B敏感性。在存在HpMNN基因的情况下,酿酒酵母mnn9缺失突变体的潮霉素B敏感性得到了互补。多形汉逊酵母同源物的DNA序列已提交给GenBank,登录号为AF264786。

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