Respiratory terminal oxidases in the facultative chemoheterotrophic and dinitrogen fixing cyanobacterium Anabaena variabilis strain ATCC 29413: characterization of the cox2 locus.

Dietmar Pils, Corinna Wilken, Ana Valladares, Enrique Flores, Georg Schmetterer
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引用次数: 17

Abstract

Upon nitrogen step-down, some filamentous cyanobacteria differentiate heterocysts, cells specialized for dinitrogen fixation, a highly oxygen sensitive process. Aerobic respiration is one of the mechanisms responsible for a microaerobic environment in heterocysts and respiratory terminal oxidases are the key enzymes of the respiratory chains. We used Anabaena variabilis strain ATCC 29413, because it is one of the few heterocyst-forming facultatively chemoheterotrophic cyanobacteria amenable to genetic manipulation. Using PCR with degenerate primers, we found four gene loci for respiratory terminal oxidases, three of which code for putative cytochrome c oxidases and one whose genes are homologous to cytochrome bd-type quinol oxidases. One cytochrome c oxidase, Cox2, was the only enzyme whose expression, tested by RT-PCR, was evidently up-regulated in diazotrophy, and therefore cloned, sequenced, and characterized. Up-regulation of Cox2 was corroborated by Northern and primer extension analyses. Strains were constructed lacking Cox1 (a previously characterized cytochrome c oxidase), Cox2, or both, which all grew diazotrophically. In vitro cytochrome c oxidase and respiratory activities were determined in all strains, allowing for the first time to estimate the relative contributions to total respiration of the different respiratory electron transport branches under different external conditions. Especially adding fructose to the growth medium led to a dramatic enhancement of in vitro cytochrome c oxidation and in vivo respiratory activity without significantly influencing gene expression.

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兼性化养异养和固氮蓝藻变水藻ATCC 29413呼吸末端氧化酶:cox2位点的表征
当氮下降时,一些丝状蓝藻分化为异囊,这些细胞专门用于二氮固定,这是一个高度氧敏感的过程。有氧呼吸是杂囊形成微氧环境的机制之一,呼吸末端氧化酶是呼吸链的关键酶。我们使用变水蓝藻菌株ATCC 29413,因为它是少数能形成异囊的兼性化异养蓝藻之一,适合于基因操作。利用简并引物,我们发现了4个呼吸末端氧化酶基因位点,其中3个编码细胞色素c氧化酶,1个基因与细胞色素bd型喹啉氧化酶同源。通过RT-PCR检测,细胞色素c氧化酶Cox2是唯一在重氮化过程中表达明显上调的酶,因此被克隆、测序和表征。Northern和引物延伸分析证实了Cox2的上调。构建缺乏Cox1(先前表征的细胞色素c氧化酶),Cox2或两者的菌株,它们都是重氮营养生长的。测定了所有菌株的体外细胞色素c氧化酶和呼吸活性,首次估计了不同外部条件下不同呼吸电子传递分支对总呼吸的相对贡献。特别是在生长培养基中添加果糖,在不显著影响基因表达的情况下,显著增强了体外细胞色素c氧化和体内呼吸活性。
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