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白色念珠菌交替氧化酶编码基因家族的特征分析

Characterization of the gene family encoding alternative oxidase from Candida albicans.

作者信息

Huh W K, Kang S O

机构信息

Laboratory of Biophysics, School of Biological Sciences, Seoul National University, Seoul 151-742, Republic of Korea, and Institute of Microbiology, Seoul National University, Seoul 151-742, Republic of Korea.

出版信息

Biochem J. 2001 Jun 1;356(Pt 2):595-604. doi: 10.1042/0264-6021:3560595.

Abstract

Candida albicans possesses a cyanide-resistant respiratory pathway mediated by alternative oxidase (AOX), which seems to be encoded by a gene family with two members. Cloning and expression of AOX1a, one of the genes encoding alternative oxidase from C. albicans, has previously been reported [Huh and Kang (1999) J. Bacteriol. 181, 4098-4102]. In the present study we report the isolation of another gene coding for alternative oxidase, designated AOX1b. AOX1b contains a continuous open reading frame that encodes a polypeptide consisting of 365 amino acids. Interestingly, AOX1a and AOX1b were found to be located in tandem on one of the chromosomes of C. albicans. The presence of cyanide in the culture medium remarkably retarded the growth of the aox1a/aox1a mutants. The growth of the aox1b/aox1b mutants and the aox1a/aox1a aox1b/aox1b double mutants was almost completely inhibited in the same medium. beta-Galactosidase reporter assays indicated that, whereas AOX1a was expressed constitutively, the expression of AOX1b was dependent on growth phase and was induced by treatment with cyanide, antimycin A, H(2)O(2), menadione and paraquat. Growth of the cells in media with non-fermentable carbon sources also enhanced the expression of AOX1b. CaSLN1, which encodes a histidine kinase, seems to be involved in the regulation of AOX expression in C. albicans on the basis of the observation that the activity of cyanide-resistant respiration and the expression level of AOX in the casln1/casln1 mutants were found to be significantly low under normal conditions and slightly increased in the presence of respiratory inhibitors compared with the wild-type strain. Like AOX1a, AOX1b could also be functionally expressed in AOX-deficient Saccharomyces cerevisiae and confer cyanide-resistant respiration on the organism.

摘要

白色念珠菌拥有一条由交替氧化酶(AOX)介导的抗氰呼吸途径,该途径似乎由一个包含两个成员的基因家族编码。之前已有报道白色念珠菌中编码交替氧化酶的基因之一AOX1a的克隆与表达[胡和康(1999年),《细菌学杂志》181卷,4098 - 4102页]。在本研究中,我们报道了另一个编码交替氧化酶的基因的分离,命名为AOX1b。AOX1b包含一个连续的开放阅读框,其编码一个由365个氨基酸组成的多肽。有趣的是,发现AOX1a和AOX1b在白色念珠菌的一条染色体上串联排列。培养基中氰化物的存在显著阻碍了aox1a/aox1a突变体的生长。在相同培养基中,aox1b/aox1b突变体和aox1a/aox1a aox1b/aox1b双突变体的生长几乎完全受到抑制。β-半乳糖苷酶报告基因检测表明,AOX1a组成型表达,而AOX1b的表达依赖于生长阶段,并可被氰化物、抗霉素A、H₂O₂、甲萘醌和百草枯处理诱导。在含有不可发酵碳源的培养基中细胞生长也增强了AOX1b的表达。基于在正常条件下casln1/casln1突变体中抗氰呼吸活性和AOX表达水平显著较低,且与野生型菌株相比在呼吸抑制剂存在时略有增加这一观察结果,编码组氨酸激酶的CaSLN1似乎参与了白色念珠菌中AOX表达的调控。与AOX1a一样,AOX1b也能在缺乏AOX的酿酒酵母中功能性表达,并赋予该生物体抗氰呼吸能力。

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