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Control of the shift from homolactic acid to mixed-acid fermentation in Lactococcus lactis: predominant role of the NADH/NAD+ ratio.

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TLDR
During batch growth of Lactococcus lactis subsp.
Abstract
During batch growth of Lactococcus lactis subsp. lactis NCDO 2118 on various sugars, the shift from homolactic to mixed-acid metabolism was directly dependent on the sugar consumption rate. This orientation of pyruvate metabolism was related to the flux-controlling activity of glyceraldehyde-3-phosphate dehydrogenase under conditions of high glycolytic flux on glucose due to the NADH/NAD+ ratio. The flux limitation at the level of glyceraldehyde-3-phosphate dehydrogenase led to an increase in the pool concentrations of both glyceraldehyde-3-phosphate and dihydroxyacetone-phosphate and inhibition of pyruvate formate lyase activity. Under such conditions, metabolism was homolactic. Lactose and to a lesser extent galactose supported less rapid growth, with a diminished flux through glycolysis, and a lower NADH/NAD+ ratio. Under such conditions, the major pathway bottleneck was most probably at the level of sugar transport rather than glyceraldehyde-3-phosphate dehydrogenase. Consequently, the pool concentrations of phosphorylated glycolytic intermediates upstream of glyceraldehyde-3-phosphate dehydrogenase decreased. However, the intracellular concentration of fructose-1,6-bisphosphate remained sufficiently high to ensure full activation of lactate dehydrogenase and had no in vivo role in controlling pyruvate metabolism, contrary to the generally accepted opinion. Regulation of pyruvate formate lyase activity by triose phosphates was relaxed, and mixed-acid fermentation occurred (no significant production of lactate on lactose) due mostly to the strong inhibition of lactate dehydrogenase by the in vivo NADH/NAD+ ratio.

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Citations
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Journal ArticleDOI

Factors affecting the fermentative lactic acid production from renewable resources1

TL;DR: Parameters affecting the fermentative lactic acid (LA) production are summarized and discussed: microorganism, carbon- and nitrogen-source, fermentation mode, pH, and temperature.
Journal ArticleDOI

Modeling Lactococcus lactis using a genome-scale flux model

TL;DR: A genome-scale flux model able to simulate and analyze network capabilities and whole-cell function under aerobic and anaerobic continuous cultures and for integration with other types of 'omic' data is developed to assist in finding new information on cellular organization and function.
Journal ArticleDOI

Practical implications of lactate and pyruvate metabolism by lactic acid bacteria in food and beverage fermentations

TL;DR: The metabolism of pyruvate and lactate by lactic acid bacteria involved in food and beverage fermentations is reviewed with an emphasis on practical implications.
Journal ArticleDOI

A review on Lactococcus lactis: from food to factory.

TL;DR: Recent technological advancements, challenges, future prospects and current diversified examples on the use of L. lactis as a live delivery vector for the administration of therapeutics against both communicable and non-communicable diseases are reviewed.
References
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Journal Article

Protein Measurement with the Folin Phenol Reagent

TL;DR: Procedures are described for measuring protein in solution or after precipitation with acids or other agents, and for the determination of as little as 0.2 gamma of protein.
Journal ArticleDOI

Carbohydrate metabolism in lactic acid bacteria.

TL;DR: An overview of the following topics is given: main pathways of homo- and heterofermentation of hexoses, i.e. glycolysis, bifidus pathway, 6-phosphogluconate pathway; uptake and dissimilation of lactose (tagatose pathway); fermentation of pentoses and pentitols; alternative fates of pyruvate.
Journal ArticleDOI

Change from Homo- to Heterolactic Fermentation by Streptococcus lactis Resulting from Glucose Limitation in Anaerobic Chemostat Cultures

TL;DR: Lactic streptococci, classically regarded as homolactic fermenters of glucose and lactose, became heterolactic when grown with limiting carbohydrate concentrations in a chemostat, indicating that fine control of enzyme activity is an important factor in the fermentation change.
Journal ArticleDOI

Regulation of lactate dehydrogenase and change of fermentation products in streptococci.

T Yamada, +1 more
TL;DR: Results indicate that changes in the intracellular level of FDP regulate LDH activity, which in turn influences the type of fermentation products produced by streptococci.
Journal ArticleDOI

Galactose fermentation by Streptococcus lactis and Streptococcus cremoris: pathways, products, and regulation.

TL;DR: All of the lactic streptococci examined except Streptococcus lactis ML8 fermented galactose to lactate, formate, acetate, and ethanol, and reduced intracellular levels of both the lactate dehydrogenase activator and pyruvate-formate lyase inhibitors appeared to be the main factors involved in the diversion of lactate to the other products.
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