Literature DB >> 3139055

Role of malolactic fermentation in lactic acid bacteria.

P Renault1, C Gaillardin, H Heslot.   

Abstract

Although decarboxylation of malate to lactate by malolactic enzyme does not liberate biologically available energy (e.g., ATP, NADH), the growth rate of many malolactic bacteria is greatly enhanced by malolactic fermentation. The deacidification of the medium due to malate dissipation cannot fully account for this situation. The chemiosmotic theory postulates that another form of energy could generated by translocation of protons through the membrane coupled to end-product efflux. Konings et al. showed that this theory is indeed applicable to lactate efflux in Streptococcus cremoris at pH 7.0. A similar mechanism could account for the observed increased activity in malolactic bacteria. The study in wild type and mutant strains of Streptococcus lactis unable to carry out malolactic fermentation led us to the following conclusions: (1) under glucose non-limiting conditions, malolactic fermentation helps to maintain pH of the medium at a certain level; (2) during glucose limited growth, malolactic fermentation could be coupled with an energetic process independent from that mentioned above.

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Year:  1988        PMID: 3139055     DOI: 10.1016/0300-9084(88)90210-6

Source DB:  PubMed          Journal:  Biochimie        ISSN: 0300-9084            Impact factor:   4.079


  12 in total

Review 1.  Surviving the acid test: responses of gram-positive bacteria to low pH.

Authors:  Paul D Cotter; Colin Hill
Journal:  Microbiol Mol Biol Rev       Date:  2003-09       Impact factor: 11.056

2.  Electrogenic malate uptake and improved growth energetics of the malolactic bacterium Leuconostoc oenos grown on glucose-malate mixtures.

Authors:  P Loubiere; P Salou; M J Leroy; N D Lindley; A Pareilleux
Journal:  J Bacteriol       Date:  1992-08       Impact factor: 3.490

3.  The efflux of a fluorescent probe is catalyzed by an ATP-driven extrusion system in Lactococcus lactis.

Authors:  D Molenaar; H Bolhuis; T Abee; B Poolman; W N Konings
Journal:  J Bacteriol       Date:  1992-05       Impact factor: 3.490

4.  Product of the Lactococcus lactis gene required for malolactic fermentation is homologous to a family of positive regulators.

Authors:  P Renault; C Gaillardin; H Heslot
Journal:  J Bacteriol       Date:  1989-06       Impact factor: 3.490

5.  Malic enzyme and malolactic enzyme pathways are functionally linked but independently regulated in Lactobacillus casei BL23.

Authors:  José María Landete; Sergi Ferrer; Vicente Monedero; Manuel Zúñiga
Journal:  Appl Environ Microbiol       Date:  2013-07-08       Impact factor: 4.792

6.  Physiological and transcriptional response of Lactobacillus casei ATCC 334 to acid stress.

Authors:  Jeff R Broadbent; Rebecca L Larsen; Virginia Deibel; James L Steele
Journal:  J Bacteriol       Date:  2010-03-05       Impact factor: 3.490

7.  Transcriptome analysis of probiotic Lactobacillus casei Zhang during fermentation in soymilk.

Authors:  Ji-Cheng Wang; Wen-Yi Zhang; Zhi Zhong; Ai-Bin Wei; Qiu-Hua Bao; Yong Zhang; Tian-Song Sun; Andrew Postnikoff; He Meng; He-Ping Zhang
Journal:  J Ind Microbiol Biotechnol       Date:  2011-07-22       Impact factor: 3.346

8.  Electrogenic L-malate transport by Lactobacillus plantarum: a basis for energy derivation from malolactic fermentation.

Authors:  E B Olsen; J B Russell; T Henick-Kling
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

9.  Malolactic fermentation: electrogenic malate uptake and malate/lactate antiport generate metabolic energy.

Authors:  B Poolman; D Molenaar; E J Smid; T Ubbink; T Abee; P P Renault; W N Konings
Journal:  J Bacteriol       Date:  1991-10       Impact factor: 3.490

10.  Anaerobic fumarate transport in Escherichia coli by an fnr-dependent dicarboxylate uptake system which is different from the aerobic dicarboxylate uptake system.

Authors:  P Engel; R Krämer; G Unden
Journal:  J Bacteriol       Date:  1992-09       Impact factor: 3.490

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