Skip to main content
Log in

Condensed phosphate deposition, sulfur amino acid use, and unidirectional transsulfuration in Synechococcus leopoliensis

  • Original Papers
  • Published:
Archives of Microbiology Aims and scope Submit manuscript

Abstract

Cells of the cyanobacterium, Synechococcus leopoliensis, have previously been shown to exhibit diminished growth, increased condensed phosphate accumulation, enlarged polyphosphate bodies, and severe chlorosis when cultured under conditions of sulfur deficiency. These characteristics were used to identify which of several sulfur amino acids and a tripeptide served as a sole sulfur source for this unicellular microorganism. Completely serving sulfur compounds were l-cystine, dl-lanthionine, l-djenkolic acid, and glutathione. Sulfur amino acids serving poorly or not at all were l-cystathionine, dl-homocystine, l-methionine, l-cysteic acid, and taurine. This pattern of use suggests that the unidirectional transsulfuration pathway demonstrated in enteric bacteria and green plants, i.e. l-cysteine to l-homocysteine, operates as well in cyanobacteria of the Synechococcus type.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  • Allen MM (1968a) Simple conditions for growth of unicellular blue-green algae on plates. J Phycol 4:1–4

    Google Scholar 

  • Allen MM (1968b) Photosynthetic membrane system in Anacystis nidulans. J Bacteriol 96:836–841

    Google Scholar 

  • Callow ME, Evans LV (1979) Polyphosphate accumulation in sulphur-starved cells of Rhodella maculata. Br Phycol J 14:327–337

    Google Scholar 

  • Carr NG (1973) Metabolic control and autotrophic physiology. In: Carr NG, Whitton BA (eds) The biology of the blue-green algae. University of California Press, Berkeley Los Angeles, pp39–65

    Google Scholar 

  • Dang AQ, Cook DE (1977) The transsulfuration pathway in Tetrahymena pyriformis. Biochim Biophys Acta 496:264–271

    Google Scholar 

  • Datko AH, Giovanelli J, Mudd SH (1974) Homocysteine biosynthesis in green plants. O-Phosphohomoserine as the physiological substrate for cystathionine γ-synthase. J Biol Chem 249:1139–1155

    Google Scholar 

  • Delaney SF, Dickson A, Carr NG (1973) The control of homoserine-O-transsuccinylase in a methionine-requiring mutant of the blue-green alga Anacystis nidulans. J Gen Microbiol 79:89–94

    Google Scholar 

  • Delavier-Klutchko C, Flavin M (1965) Role of a bacterial cystathionine β-cleavage enzyme in disulfide decomposition. Biochim Biophys Acta 99:375–377

    Google Scholar 

  • Diessner W, Schmidt A (1981) Isoenzymes of cysteine synthase in the cyanobacterium Synechococcus 6301. Z Pflanzenphysiol 102:57–68

    Google Scholar 

  • Doolittle WF (1979) The cyanobacterial genome, its expression, and the control of that expression. Adv Microbial Physiol 20:1–102

    Google Scholar 

  • Ellis RJ, Humphries SK, Pasternak CA (1964) Repressors of sulphate activation in Escherichia coli. Biochem J 92:167–172

    Google Scholar 

  • Fahey RC, Brown WC, Adams WB, Worsham MB (1978) Occurrence of glutathione in bacteria. J Bacteriol 133:1126–1129

    Google Scholar 

  • Flavin M (1975) Methionine biosynthesis. In: Greenberg DM (ed) Metabolism of sulphur compounds. Metabolic pathways, vol VII. Academic Press, New York, pp 457–503

    Google Scholar 

  • Giovanelli J, Mudd SH (1971) Transsulfuration in higher plants. Partial purification and properties of β-cystathionase of spinach. Biochem Biophys Res Comm 27:150–156

    Google Scholar 

  • Giovanelli J, Mudd SH, Datko AH (1978) Homocysteine synthesis in green plants. Physiological importance of the transsulfuration pathway in Chlorella sorokiniana growing under steady state conditions with limiting sulfate. J Biol Chem 253:5665–5677

    Google Scholar 

  • Greenberg DM (1975) Biosynthesis of cysteine and cystine. In: Greenberg DM (ed) Metabolism of sulfurcompounds. Metabolic pathways, vol VII. Academic Press, New York, pp 505–528

    Google Scholar 

  • Grillo JF, Gibson J (1979) Regulation of phosphate accumulation in the unicellular cyanobacterium Synechococcus. J Bacteriol 140:508–517

    Google Scholar 

  • Guggenheim S, Flavin M (1969) Cystathionine γ-synthase. A pyridoxal phosphate enzyme catalyzing rapid exchanges of β and α hydrogen atoms in amino acids. J Biol Chem 244:6217–6227

    Google Scholar 

  • Hall G, Flick MB, Jensen RA (1980) Approach to recognition of regulatory mutants of cyanobacteria. J Bacteriol 143:481–488

    Google Scholar 

  • Harold FM, Sylvan S (1963) Accumulation of inorganic polyphosphate in Aerobacter aerogenes. II. Environmental control and the role of sulfur compounds. J Bacteriol 86:222–231

    Google Scholar 

  • Ingram LO, Pierson D, Kane JF, Van Baalen C, Jensen RA (1972) Documentation of auxotrophic mutation in blue-green bacteria: characterization of a tryptophan auxotroph in Agmenellum quadruplicatum. J Bacteriol 111:112–118

    Google Scholar 

  • Kaney LO, Jhabvala P (1975) Absence of repression in a phenylalanine auxotroph of Synechococcus cedrorum. J Gen Microbiol 87:370–372

    Google Scholar 

  • Kredich NM (1971) Regulation of l-cysteine biosynthesis in Salmonella typhimurium. J Biol Chem 246:3474–3484

    Google Scholar 

  • Kulaev IS, Vagabov VM (1983) Polyphosphate metabolism in micro-organisms. Adv Microbiol Physiol 24:83–171

    Google Scholar 

  • Lawry NH, Jensen TE (1979) Deposition of condensed phosphate as an effect of varying sulfur deficiency in the cyanobacterium Synechococcus sp. (Anacystis nidulans). Arch Microbiol 120:1–7

    Google Scholar 

  • Lawry NH, Simon RD (1982) The normal and induced occurrence of cyanophycin inclusion bodies in several blue-green algae. J Phycol 18:391–399

    Google Scholar 

  • Maclean FI, Forrest HS, Myers J (1965) Origin of the side chain in pteridines of the biopterin type. Biochem Biophys Res Comm 18:623–626

    Google Scholar 

  • Miller LS, Holt SC (1977) Effect of carbon dioxide on pigment and membrane content of Synechococcus lividus. Arch Microbiol 115:185–198

    Google Scholar 

  • Murphy J, Riley JP (1962) A modified single solution method for the determination of phosphate in natural waters. Anal Chim Acta 27:31–36

    Google Scholar 

  • Pearce J, Carr NG (1967) The metabolism of acetate by the blue-green algae, Anabaena variabilis and Anacystis nidulans. J Gen Microbiol 49:301–313

    Google Scholar 

  • Pelroy RA, Rippka R, Stanier RY (1972) Metabolism of glucose by unicellular blue-green algae. Arch Mikrobiol 87:303–322

    Google Scholar 

  • Pine MJ (1963) Alcohol-soluble protein of microorganisms. J Bacteriol 85:301–305

    Google Scholar 

  • Rippka R, Deruelles J, Waterbury JB, Herdman M, Stanier RY (1979) Generic assignments, strain histories and properties of pure cultures of cyanobacteria. J Gen Microbiol 111:1–61

    Google Scholar 

  • Schmidt A, Kramer E (1983) A membrane-bound cysteine oxydase from the cyanobacterium Synechococcus 6301. Z Naturforsch C 38:446–450

    Google Scholar 

  • Shimamoto G, Berk RS (1980) Taurine catabolism. III. Evidence for the participation of the glyoxylate cycle. Biochim Biophys Acta 632:399–407

    Google Scholar 

  • Singer RA, Doolittle WF (1975) Leucine biosynthesis in the blue-green bacterium Anacystis nidulans. J Bacteriol 124:810–814

    Google Scholar 

  • Smith AJ, Hoare DS (1977) Specialists phototrophs, lithotrophs, and methylotrophs: a unity among a diversity of procaryotes? Bacteriol Rev 41:419–448

    Google Scholar 

  • Smith AJ, London J, Stanier RY (1967) Biochemical basis of obligate autotrophy in blue-green algae and thiobacilli. J Bacteriol 94:972–983

    Google Scholar 

  • Smith DA (1971) S-amino acid metabolism and its regulation in Escherichia coli and Salmonella typhimurium. Adv Genet 16:141–165

    Google Scholar 

  • Smith IW (1969) Chromatographic and electrophoretic techniques, vol 1 (chromatography), 3rd edn. Interscience, New York, pp 104–142

    Google Scholar 

  • Smith IW, Wilkinson JG, Duguid JP (1954) Volutin production in Aerobacter aerogenes due to nutrient imbalance. J Bacteriol 68:450–463

    Google Scholar 

  • Stapley EO, Starkey RL (1970) Decomposition of cysteic acid and taurine by soil micro-organisms. J Gen Microbiol 64:77–84

    Google Scholar 

  • Udvardy J, Balogh Á, Farkas GL (1983) Modulation of glyceraldehyde-3-phosphate dehydrogenase in Anacystis nidulans by glutathione. Arch Microbiol 133:2–5

    Google Scholar 

  • Wood NB, Haselkorn R (1980) Control of phycobiliprotein proteolysis and heterocyst differentiation in Anabaena. J Bacteriol 141:1375–1385

    Google Scholar 

  • Wyman M, Gregory RPF, Carr NG (1985) Novel role for phycoerythrin in a marine cyanobacterium, Synechococcus strain DC2. Science 230:818–820

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Lawry, N.H., Jensen, T.E. Condensed phosphate deposition, sulfur amino acid use, and unidirectional transsulfuration in Synechococcus leopoliensis . Arch. Microbiol. 144, 317–323 (1986). https://doi.org/10.1007/BF00409879

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00409879

Key words

Navigation