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丝状蓝细菌多变鱼腥藻ATCC 29413中编码铁氧化还原蛋白的fdxN基因对于固氮作用并非必需。

The ferredoxin-encoding fdxN gene of the filamentous cyanobacterium Anabaena variabilis ATCC 29413 is not essential for nitrogen fixation.

作者信息

Masepohl Bernd, Görlitz Kirsten, Monnerjahn Ursula, Moslerand Britta, Böhme Herbert

机构信息

Botanisches Institut der Universität Bonn, Kirschallee 1, D-53115 Bonn, Germany.

出版信息

New Phytol. 1997 Jul;136(3):419-423. doi: 10.1046/j.1469-8137.1997.00771.x.

Abstract

In contrast to that of Anabaena sp. PCC7120, the fdxN gene in Anabaena variabilis ATCC 29413 is not interrupted by a 55-kb DNA element, making this strain more suitable for genetic analysis of fdxN independent of the developmentally regulated excision during heterocyst formation. As a basis for mutational analysis, the fdxN gene of A. variabilis was cloned and sequenced. The deduced FdxN protein sequence was highly homologous to the Anabaena 7120 fdxN gene product including eight cysteine residues that are known to be conserved among ferredoxins containing two [4Fe-4S] clusters. The fdxN gene of A. variabilis was disrupted by insertion of an interposon within the fdxN coding region resulting in mutant strain KG29. Diazotrophic growth and in vivo nitrogenase activity of KG29 were similar to those of the wild-type, indicating that FdxN was not essential for N fixation in A. variabilis.

摘要

与鱼腥藻属(Anabaena sp.)PCC7120不同,多变鱼腥藻(Anabaena variabilis)ATCC 29413中的fdxN基因未被一个55 kb的DNA元件中断,这使得该菌株更适合对fdxN进行遗传分析,而不受异形胞形成过程中发育调控切除的影响。作为突变分析的基础,克隆并测序了多变鱼腥藻的fdxN基因。推导的FdxN蛋白序列与鱼腥藻7120的fdxN基因产物高度同源,包括八个半胱氨酸残基,已知这些残基在含有两个[4Fe-4S]簇的铁氧化还原蛋白中是保守的。通过在fdxN编码区内插入一个转座子破坏了多变鱼腥藻的fdxN基因,产生了突变菌株KG29。KG29的固氮生长和体内固氮酶活性与野生型相似,表明FdxN对多变鱼腥藻的固氮作用不是必需的。

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