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PMID: 12180931 Published · ppublish English Journal Article

Dynamic response of catabolic pathways to autoacidification in Lactococcus lactis: transcript profiling and stability in relation to metabolic and energetic constraints.

Molecular microbiology ·Vol. 45 ·No. 4 ·2002-08-00 ·Pages 1143-52

Even S, Lindley ND, Loubière P, Cocaign-Bousquet M

Abstract

The dynamic response of the central metabolic pathways to autoacidification (accumulation of organic acid fermentation products) in Lactococcus lactis was investigated in a global manner by integrating molecular data (cellular transcript concentrations, mRNA turnover) within physiological investigations of metabolic and energetic parameters. The decrease in pH associated with the accumulation of organic acids modified the physiological state of the cell considerably. Cytoplasmic acidification led to inhibition of enzyme activities and, consequently, to a diminished catabolic flux through glycolysis and a decreased rate of biochemical energy synthesis. This decrease in energy production together with the increased energy expenditure to counter cytoplasmic acidification led to energetic limitations for biomass synthesis. In these conditions, the specific growth rate decreased progressively, and growth ultimately stopped, although a diminished catabolic flux was maintained in the absence of growth. The cellular response to this phenomenon was to maintain significant levels of mRNA of catabolic genes, involving both continued transcription of the genes and also, in certain cases, an increase in transcript stability. Thus, translation was maintained, and intracellular concentration of certain enzymes increased, partially compensating for the inhibition of activity provoked by the diminished pH. When catabolic activity ceased after prolonged exposure to stress-induced stationary phase, endogenous RNA catabolism was observed.

MeSH Terms
Acids/metabolism Energy Metabolism Hydrogen-Ion Concentration Kinetics Lactococcus lactis/enzymology,genetics,metabolism Nucleic Acid Hybridization Polymerase Chain Reaction RNA, Bacterial/genetics,metabolism RNA, Messenger/genetics,metabolism
Chemicals
Acids RNA, Bacterial RNA, Messenger
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Even Sergine
Laboratorie Biotechnologie-Bioprocédés, UMR 5504 INSA/CNRS and UMR 792 INSA/INRA, Centre de Bioingénierie Gilbert Durand, Institute National des Sciences Appliquées, Toulouse, France.
Lindley Nic D
Loubière Pascal
Cocaign-Bousquet Muriel
Article Info
Journal
Molecular microbiology
Abbr.
Mol Microbiol
ISSN
0950-382X
Published
2002-08-00
Pages
1143-52
Language
English
Region
England
NLM ID
8712028
Subset
IM
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