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白色念珠菌几丁质酶基因的分子克隆与特性分析

Molecular cloning and characterization of chitinase genes from Candida albicans.

作者信息

McCreath K J, Specht C A, Robbins P W

机构信息

Center for Cancer Research, Massachusetts Institute of Technology, Cambridge 02139, USA.

出版信息

Proc Natl Acad Sci U S A. 1995 Mar 28;92(7):2544-8. doi: 10.1073/pnas.92.7.2544.

Abstract

Chitinase (EC 3.2.1.14) is an important enzyme for the remodeling of chitin in the cell wall of fungi. We have cloned three chitinase genes (CHT1, CHT2, and CHT3) from the dimorphic human pathogen Candida albicans. CHT2 and CHT3 have been sequenced in full and their primary structures have been analyzed: CHT2 encodes a protein of 583 aa with a predicted size of 60.8 kDa; CHT3 encodes a protein of 567 aa with a predicted size of 60 kDa. All three genes show striking similarity to other chitinase genes in the literature, especially in the proposed catalytic domain. Transcription of CHT2 and CHT3 was greater when C. albicans was grown in a yeast phase as compared to a mycelial phase. A transcript of CHT1 could not be detected in either growth condition.

摘要

几丁质酶(EC 3.2.1.14)是一种对真菌细胞壁中几丁质重塑起重要作用的酶。我们从双态性人类病原体白色念珠菌中克隆了三个几丁质酶基因(CHT1、CHT2和CHT3)。CHT2和CHT3已完成全序列测定并分析了其一级结构:CHT2编码一个由583个氨基酸组成的蛋白质,预测大小为60.8 kDa;CHT3编码一个由567个氨基酸组成的蛋白质,预测大小为60 kDa。所有这三个基因与文献中其他几丁质酶基因都有显著相似性,尤其是在推测的催化结构域。与菌丝体阶段相比,白色念珠菌在酵母阶段生长时,CHT2和CHT3的转录水平更高。在两种生长条件下均未检测到CHT1的转录本。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a92/42254/ec97d057f8bf/pnas01485-0137-a.jpg

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