4.5 Article

Conversion of Corynebacterium glutamicum from an aerobic respiring to an aerobic fermenting bacterium by inactivation of the respiratory chain

期刊

BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
卷 1827, 期 6, 页码 699-708

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ELSEVIER
DOI: 10.1016/j.bbabio.2013.02.004

关键词

Corynebacterium glutamicum; Cytochrome bd oxidase; Cytochrome bc(1) complex; Cytochrome aa(3) oxidase; Proton-motive force; Maintenance coefficient

资金

  1. Bundesministerium fur Bildung und Forschung (BMBF) [0315598A]

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In this study a comparative analysis of three Corynebacterium glutamicum ATCC 13032 respiratory chain mutants lacking either the cytochrome bd branch (Delta cydAB), or the cytochrome bc(1)-aa(3) branch (Delta qcr), or both branches was performed. The lack of cytochrome bd oxidase was inhibitory only under conditions of oxygen limitation, whereas the absence of a functional cytochrome bc(1)-aa(3) supercomplex led to decreases in growth rate, biomass yield, respiration and proton-motive force (pmf) and a strongly increased maintenance coefficient under oxygen excess. These results show that the bc(1)-aa(3) supercomplex is of major importance for aerobic respiration. For the first time, a C. glutamicum strain with a completely inactivated aerobic respiratory chain was obtained (Delta cydAB Delta qcr), named DOOR (devoid of oxygen respiration), which was able to grow aerobically in BHI (brain-heart infusion) glucose complex medium with a 70% reduced biomass yield compared to the wild type. Surprisingly, reasonable aerobic growth was also possible in glucose minimal medium after supplementation with peptone. Under these conditions, the DOOR strain displayed a fermentative type of catabolism with L-lactate as major and acetate and succinate as minor products. The DOOR strain had about 2% of the oxygen consumption rate of the wild type, showing the absence of additional terminal oxidases. The pmf of the DOOR mutant was reduced by about 30% compared to the wild type. Candidates for pmf generation in the DOOR strain are succinate:menaquinone oxidoreductase, which probably can generate pmf in the direction of fumarate reduction, and F1FO-ATP synthase, which can couple ATP hydrolysis to the export of protons. (c) 2013 Elsevier B.V. All rights reserved.

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