Strains of yeast with increased rates of glycolysis

Chemistry: molecular biology and microbiology – Treatment of micro-organisms or enzymes with electrical or... – Modification of viruses

Patent

Rate now

  [ 0.00 ] – not rated yet Voters 0   Comments 0

Details

43525421, 435194, 435161, 4353201, C12N 1563, C12N 119

Patent

active

052682854

ABSTRACT:
The present invention provides a process for increasing the rate of production of carbon dioxide, ethanol and other fermentation products such as citric acid, produced by yeast such as Saccharomyces cerevisiae during fermentation, and decreasing biomass production by regulating the rate of glycolysis indirectly through changing the energy balance of the cell, i.e., by reducing intracellular ATP levels. Modifications for so altering the glycolysis rate involve the use of either a regulated ATP hydrolysis within the cell or a regulated leakage of ATP from the cell. This invention encompasses several ways for altering the yeast ATP level including (a) engaging futile metabolic cycles to increase ATP consumption; and (b) using an altered exocellular acid phosphatase so that it becomes intracellular to increase intracellular ATP hydrolysis; by which alterations in the ATP level may be turned off during growth of the yeast on a commercial scale, and then turned on before or during, and preferably before or at a very early stage of, the dough-rising phase.

REFERENCES:
Sekikawa et al., "Defects in functional expression of an influenza virus hemogglutinin lacking the signal peptide sequences," PNAS, 80:3563-3567 (Jun. 1983).
Ke et al., "Molecular structure of fructose-1,6-bisphosphotase at 2.8-.ANG. resolution," PNAS, 86:1475-1479 (Mar. 1989).
Foy et al., "Concentration of Metabolites and the Regulation of Phosphofructo-Kinases and Fructose-1,6-Bisphosphotase in Saccharomyces cerevisiae," Archives of Microbiology, 129(3):216-220 (1981).
Arima et al., "The nucleotide sequence of the yeast PHO5 gene: a putative precursor of repressible acid phosphotase contains a signal peptide," Nucleic Acids Research, 11(6):1657-1673 (1983).
Noda et al. "Characterization of Fructose 1,6-bisphosphatase from Bakers' Yeast" Journal of Biological Chemistry 259(11):7191-97 (Jun. 1984).
Mazon et al. "Inactivation of Yeast Fructose-1,6-bisphophatase" Journal of Biological Chemistry 257(3):1128-1130 (Feb. 1982).
McLeod et al. "Components of the Site-specific Recombination System encoded by the Yeast Plasmid 2-.mu. Circle," Cold Spring Harbor Symposia on Quantitative Biology 49:779-784 (1984).
Zoller et al. "Oligonucleotide-Directed Mutagenesis of DNA fragments cloned into M13 vectors" Methods in Enzymology 100:468-500 (1983).
Kingsman et al. "Heterologous Gene Expression in S. cervisiae" Biotechnology and Genetic Engineering Reviews 3:377-416 (Sep. 1985).
Albert L. Lehninger, "Biochemistry" 2nd Edition, pp. 235-236, 437-438, and 630-631, Worth Publishers, Inc. (New York, 1976).
Alessio Vassarotti et al., The Journal of Biological Chemistry 260(10):6348-6353 (1985).
John M. Sedivy et al., J. Mol. Biol. 186:307-319 (1985).
Rosine Haguenauer-Tsapis et al., Molecular and Cellular Biology 4(12):2668-2675 (1984).
Anthony H. Rose et al., "The Yeasts", Physiology and Biochemistry of Yeasts, vol. 2, pp. 274-275, ed. Academic Press, London and New York 1971).

LandOfFree

Say what you really think

Search LandOfFree.com for the USA inventors and patents. Rate them and share your experience with other people.

Rating

Strains of yeast with increased rates of glycolysis does not yet have a rating. At this time, there are no reviews or comments for this patent.

If you have personal experience with Strains of yeast with increased rates of glycolysis, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Strains of yeast with increased rates of glycolysis will most certainly appreciate the feedback.

Rate now

     

Profile ID: LFUS-PAI-O-2015242

  Search
All data on this website is collected from public sources. Our data reflects the most accurate information available at the time of publication.