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. 1968 Apr;43(4):547–554. doi: 10.1104/pp.43.4.547

Studies of Sulfate Utilization by Algae. 4. Properties of a Cell-Free Sulfate-Reducing System From Chlorella 1

Jerome A Schiff 1, Mark Levinthal 1,2
PMCID: PMC1086886  PMID: 16656805

Abstract

A cell-free system from Chlorella pyrenoidosa Chick (Emerson strain 3) which produces acid-volatile radioactivity from 35SO42− is described. A high speed supernatant from cells broken in the French Press at pH 7.0 shows maximal activity when fortified with ATP, an ATP-generating system (creatine phosphate and creatine phosphokinase), TPN, a TPN-reducing system (glucose-6-phosphate and glucose-6-phosphate dehydrogenase) and MgCl2. This system is quite labile and is not stable to dialysis. Addition of low concentrations of 2,3,-dimercaptopropan-1-ol (BAL) to the buffers used for enzyme preparation stabilize the extracts and permit them to be dialyzed for 4 hours without loss of activity. If additional BAL is also added to the incubation mixtures it can replace TPNH as a reductant. DPNH also shows appreciable acticity.

The system prepared with BAL-containing buffers shows maximal activity at pH 9.0. At this pH, the system requires only ATP, Mg2+ and additional BAL and has high activity and stability compared with the other conditions tried. The optimum concentrations of these reactants has been determined and the kinetics of production of acid-volatile radioactivity are described. Nucleoside triphosphates other than ATP are not appreciably active in this system. In all cases, anaerobic conditions are required for maximal activity, the enzyme extracts are labile to heat, and no unequivocal requirement for thioctic acid can be demonstrated.

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Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. LAURENT T. C., MOORE E. C., REICHARD P. ENZYMATIC SYNTHESIS OF DEOXYRIBONUCLEOTIDES. IV. ISOLATION AND CHARACTERIZATION OF THIOREDOXIN, THE HYDROGEN DONOR FROM ESCHERICHIA COLI B. J Biol Chem. 1964 Oct;239:3436–3444. [PubMed] [Google Scholar]
  2. PECK H. D., Jr Enzymatic basis for assimilatory and dissimilatory sulfate reduction. J Bacteriol. 1961 Dec;82:933–939. doi: 10.1128/jb.82.6.933-939.1961. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Peck H. D. THE ATP-DEPENDENT REDUCTION OF SULFATE WITH HYDROGEN IN EXTRACTS OF DESULFOVIBRIO DESULFURICANS. Proc Natl Acad Sci U S A. 1959 May;45(5):701–708. doi: 10.1073/pnas.45.5.701. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. ROBBINS P. W., LIPMANN F. Separation of the two enzymatic phases in active sulfate synthesis. J Biol Chem. 1958 Sep;233(3):681–685. [PubMed] [Google Scholar]
  5. Schiff J. A. Studies of Sulfate Utilization by Algae. II. Further Identification of Reduced Compounds Formed from Sulfate by Chlorella. Plant Physiol. 1964 Mar;39(2):176–179. doi: 10.1104/pp.39.2.176. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Schiff J. A. Studies on Sulfate Utilization by Chlorella pyrenoidosa using Sulfate-S; the Occurrence of S-Adenosyl Methionine. Plant Physiol. 1959 Jan;34(1):73–80. doi: 10.1104/pp.34.1.73. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Torii K., Bandurski R. S. Yeast sulfate-reducing system. 3. An intermediate in the reduction of 3'-phosphoryl-5'-adenosinephosphosulfate to sulfite. Biochim Biophys Acta. 1967 Mar 22;136(2):286–295. doi: 10.1016/0304-4165(67)90074-8. [DOI] [PubMed] [Google Scholar]
  8. WILSON L. G., ASAHI T., BANDURSKI R. S. Yeast sulfate-reducing system. I. Reduction of sulfate to sulfite. J Biol Chem. 1961 Jun;236:1822–1829. [PubMed] [Google Scholar]
  9. Wedding R. T., Black M. K. Uptake and Metabolism of Sulfate by Chlorella. I. Sulfate Accumulation and Active Sulfate. Plant Physiol. 1960 Jan;35(1):72–80. doi: 10.1104/pp.35.1.72. [DOI] [PMC free article] [PubMed] [Google Scholar]

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