Abstract
In Lactococcus lactis subsp. cremoris FD1, galactose and lactose are both transported and phosphorylated by phosphotransferase systems. Lactose 6-phosphate (lactose-6P) is hydrolyzed intracellularly to galactose-6P and glucose. Glucose enters glycolysis as glucose-6P, whereas galactose-6P is metabolized via the tagatose-6P pathway and enters glycolysis at the tagatose diphosphate and fructose diphosphate pool. Galactose would therefore be a gluconeogenic sugar in L. lactis subsp. cremoris FD1, but since fructose 1,6-diphosphatase is not present in this strain, galactose cannot serve as an essential biomass precursor (glucose-6P or fructose-6P) but only as an energy (ATP) source. Analysis of the growth energetics shows that transition from N limitation to limitation by glucose-6P or fructose-6P gives rise to a very high growth-related ATP consumption (152 mmol of ATP per g of biomass) compared with the value in cultures which are not limited by glucose-6P or fructose-6P (15 to 50 mmol of ATP per g of biomass). During lactose metabolism, the galactose flux through the tagatose-6P pathway (rmax = 1.2 h-1) is lower than the glucose flux through glycolysis (rmax = 1.5 h-1) and intracellular galactose-6P is dephosphorylated; this is followed by expulsion of galactose. Expulsion of a metabolizable sugar has not been reported previously, and the specific rate of galactose expulsion is up to 0.61 g of galactose g of biomass -1 h-1 depending on the lactose flux and the metabolic state of the bacteria. Galactose excreted during batch fermentation on lactose is reabsorbed and metabolized when lactose is depleted from the medium. In vitro incubation of galactose-6P (50 mM) and permeabilized cells (8 g/liter) gives a supernatant containing free galactose (50 mM) but no Pi (less than 0.5 mM). No organic compound except the liberated galactose is present in sufficient concentration to bind the phosphate. Phosphate is quantitatively recovered in the supernatant as Pi by hydrolysis with alkaline phosphatase (EC 3.1.3.1), whereas inorganic pyrophosphatase (EC 3.6.1.1) cannot hydrolyze the compound. The results indicate that the unknown phosphate-containing compound might be polyphosphate.
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Selected References
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- Benthin S., Nielsen J., Villadsen J. Two Uptake Systems for Fructose in Lactococcus lactis subsp. cremoris FD1 Produce Glycolytic and Gluconeogenic Fructose Phosphates and Induce Oscillations in Growth and Lactic Acid Formation. Appl Environ Microbiol. 1993 Oct;59(10):3206–3211. doi: 10.1128/aem.59.10.3206-3211.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Bissett D. L., Anderson R. L. Lactose and D-galactose metabolism in group N streptococci: presence of enzymes for both the D-galactose 1-phosphate and D-tagatose 6-phosphate pathways. J Bacteriol. 1974 Jan;117(1):318–320. doi: 10.1128/jb.117.1.318-320.1974. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crow V. L., Davey G. P., Pearce L. E., Thomas T. D. Plasmid linkage of the D-tagatose 6-phosphate pathway in Streptococcus lactis: effect on lactose and galactose metabolism. J Bacteriol. 1983 Jan;153(1):76–83. doi: 10.1128/jb.153.1.76-83.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crow V. L., Thomas T. D. D-tagatose 1,6-diphosphate aldolase from lactic streptococci: purification, properties, and use in measuring intracellular tagatose 1,6-diphosphate. J Bacteriol. 1982 Aug;151(2):600–608. doi: 10.1128/jb.151.2.600-608.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Crow V. L., Thomas T. D. Properties of a Streptococcus lactis strain that ferments lactose slowly. J Bacteriol. 1984 Jan;157(1):28–34. doi: 10.1128/jb.157.1.28-34.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Demko G. M., Blanton S. J., Benoit R. E. Heterofermentative carbohydrate metabolism of lactose-impaired mutants of Streptococcus lactis. J Bacteriol. 1972 Dec;112(3):1335–1345. doi: 10.1128/jb.112.3.1335-1345.1972. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hickey M. W., Hillier A. J., Jago G. R. Transport and metabolism of lactose, glucose, and galactose in homofermentative lactobacilli. Appl Environ Microbiol. 1986 Apr;51(4):825–831. doi: 10.1128/aem.51.4.825-831.1986. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Hutkins R. W., Ponne C. Lactose Uptake Driven by Galactose Efflux in Streptococcus thermophilus: Evidence for a Galactose-Lactose Antiporter. Appl Environ Microbiol. 1991 Apr;57(4):941–944. doi: 10.1128/aem.57.4.941-944.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- LeBlanc D. J., Crow V. L., Lee L. N., Garon C. F. Influence of the lactose plasmid on the metabolism of galactose by Streptococcus lactis. J Bacteriol. 1979 Feb;137(2):878–884. doi: 10.1128/jb.137.2.878-884.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- McKay L., Miller A., 3rd, Sandine W. E., Elliker P. R. Mechanisms of lactose utilization by lactic acid streptococci: enzymatic and genetic analyses. J Bacteriol. 1970 Jun;102(3):804–809. doi: 10.1128/jb.102.3.804-809.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Park Y. H., McKay L. L. Distinct galactose phosphoenolpyruvate-dependent phosphotransferase system in Streptococcus lactis. J Bacteriol. 1982 Feb;149(2):420–425. doi: 10.1128/jb.149.2.420-425.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Perret J., Gay P. Kinetic study of a phosphoryl exchange reaction between fructose and fructose 1-phosphate catalyzed by the membrane-bound enzyme II of the phosphoenolpyruvate-fructose 1-phosphotransferase system of Bacillus subtilis. Eur J Biochem. 1979 Dec;102(1):237–246. doi: 10.1111/j.1432-1033.1979.tb06285.x. [DOI] [PubMed] [Google Scholar]
- Poolman B. Energy transduction in lactic acid bacteria. FEMS Microbiol Rev. 1993 Sep;12(1-3):125–147. doi: 10.1111/j.1574-6976.1993.tb00015.x. [DOI] [PubMed] [Google Scholar]
- Reizer J., Saier M. H., Jr Involvement of lactose enzyme II of the phosphotransferase system in rapid expulsion of free galactosides from Streptococcus pyogenes. J Bacteriol. 1983 Oct;156(1):236–242. doi: 10.1128/jb.156.1.236-242.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Saier M. H., Jr, Feucht B. U., Mora W. K. Sugar phosphate: sugar transphosphorylation and exchange group translocation catalyzed by the enzyme 11 complexes of the bacterial phosphoenolpyruvate: sugar phosphotransferase system. J Biol Chem. 1977 Dec 25;252(24):8899–8907. [PubMed] [Google Scholar]
- Thomas T. D., Crow V. L. Selection of Galactose-Fermenting Streptococcus thermophilus in Lactose-Limited Chemostat Cultures. Appl Environ Microbiol. 1984 Jul;48(1):186–191. doi: 10.1128/aem.48.1.186-191.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas T. D. Regulation of lactose fermentation in group N streptococci. Appl Environ Microbiol. 1976 Oct;32(4):474–478. doi: 10.1128/aem.32.4.474-478.1976. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thomas T. D., Turner K. W., Crow V. L. Galactose fermentation by Streptococcus lactis and Streptococcus cremoris: pathways, products, and regulation. J Bacteriol. 1980 Nov;144(2):672–682. doi: 10.1128/jb.144.2.672-682.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., Chassy B. M., Egan W. Lactose metabolism in Streptococcus lactis: studies with a mutant lacking glucokinase and mannose-phosphotransferase activities. J Bacteriol. 1985 Apr;162(1):217–223. doi: 10.1128/jb.162.1.217-223.1985. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., Chassy B. M. Intracellular hexose-6-phosphate:phosphohydrolase from Streptococcus lactis: purification, properties, and function. J Bacteriol. 1983 Oct;156(1):70–80. doi: 10.1128/jb.156.1.70-80.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., Chassy B. M. Novel phosphoenolpyruvate-dependent futile cycle in Streptococcus lactis: 2-deoxy-D-glucose uncouples energy production from growth. J Bacteriol. 1982 Sep;151(3):1454–1465. doi: 10.1128/jb.151.3.1454-1465.1982. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J. Galactose transport systems in Streptococcus lactis. J Bacteriol. 1980 Nov;144(2):683–691. doi: 10.1128/jb.144.2.683-691.1980. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J. Lactose metabolism in Streptococcus lactis: phosphorylation of galactose and glucose moieties in vivo. J Bacteriol. 1979 Dec;140(3):774–785. doi: 10.1128/jb.140.3.774-785.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., Saier M. H., Jr Regulation of methyl-beta-d-thiogalactopyranoside-6-phosphate accumulation in Streptococcus lactis by exclusion and expulsion mechanisms. J Bacteriol. 1981 Jun;146(3):885–894. doi: 10.1128/jb.146.3.885-894.1981. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Thompson J., Turner K. W., Thomas T. D. Catabolite inhibition and sequential metabolism of sugars by Streptococcus lactis. J Bacteriol. 1978 Mar;133(3):1163–1174. doi: 10.1128/jb.133.3.1163-1174.1978. [DOI] [PMC free article] [PubMed] [Google Scholar]
- de Vos W. M., Boerrigter I., van Rooyen R. J., Reiche B., Hengstenberg W. Characterization of the lactose-specific enzymes of the phosphotransferase system in Lactococcus lactis. J Biol Chem. 1990 Dec 25;265(36):22554–22560. [PubMed] [Google Scholar]
- van Rooijen R. J., van Schalkwijk S., de Vos W. M. Molecular cloning, characterization, and nucleotide sequence of the tagatose 6-phosphate pathway gene cluster of the lactose operon of Lactococcus lactis. J Biol Chem. 1991 Apr 15;266(11):7176–7181. [PubMed] [Google Scholar]
