4.6 Article

Oxygen-Inducible Conversion of Lactate to Acetate in Heterofermentative Lactobacillus brevis ATCC 367

Journal

APPLIED AND ENVIRONMENTAL MICROBIOLOGY
Volume 83, Issue 21, Pages -

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/AEM.01659-17

Keywords

Lactobacillus brevis; aerobic acetate accumulation; pyruvate dehydrogenase; pyruvate oxidase

Funding

  1. Public Service Sectors (Agriculture) Special and Scientific Research Projects [201503134]
  2. National Natural Science Foundation of China [31471715]
  3. National Science Foundation for Young Scientists of China [31400077]

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Lactobacillus brevis is an obligatory heterofermentative lactic acid bacterium that produces high levels of acetate, which improve the aerobic stability of si-lages against deterioration caused by yeasts and molds. However, the mechanism involved in acetate accumulation has yet to be elucidated. Here, experimental evidence indicated that aerobiosis resulted in the conversion of lactate to acetate after glucose exhaustion in L. brevis ATCC 367 (GenBank accession number NC_008497). To elucidate the conversion pathway, in silico analysis showed that lactate was first converted to pyruvate by the reverse catalytic reaction of lactate dehydrogenase (LDH); subsequently, pyruvate conversion to acetate might be mediated by pyruvate dehydrogenase (PDH) or pyruvate oxidase (POX). Transcriptional analysis indicated that the pdh and pox genes of L. brevis ATCC 367 were upregulated 37.92- and 18.32-fold, respectively, by oxygen and glucose exhaustion, corresponding to 5.32- and 2.35-fold increases in the respective enzyme activities. Compared with the wildtype strain, the transcription and enzymatic activity of PDH remained stable in the Delta pox mutant, while those of POX increased significantly in the Delta pdh mutant. More lactate but less acetate was produced in the Delta pdh mutant than in the wild-type and Delta pox mutant strains, and more H2O2 (a product of the POX pathway) was produced in the Delta pdh mutant. We speculated that the high levels of aerobic acetate accumulation in L. brevis ATCC 367 originated mainly from the reuse of lactate to produce pyruvate, which was further converted to acetate by the predominant and secondary functions of PDH and POX, respectively. IMPORTANCE PDH and POX are two possible key enzymes involved in aerobic acetate accumulation in lactic acid bacteria (LAB). It is currently thought that POX plays the major role in aerobic growth in homofermentative LAB and some heterofermentative LAB, while the impact of PDH remains unclear. In this study, we reported that both PDH and POX worked in the aerobic conversion of lactate to acetate in L. brevis ATCC 367, in dominant and secondary roles, respectively. Our findings will further develop the theory of aerobic metabolism by LAB.

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