Differential Analysis of Sulfhydryl and Disulfide Groups of Intact Spores

Author:

Blankenship L. C.1,Pallansch M. J.1

Affiliation:

1. Dairy Products Laboratory, Eastern Utilization Research and Development Division, U.S. Department of Agriculture, Washington, D.C.

Abstract

Blankenship , L. C. (Eastern Utilization Research and Development Division, Washington D.C.), and M. J. Pallansch . Differential analysis of sulfhydryl and disulfide groups of intact spores. J. Bacteriol. 92: 1615–1617. 1966.—Fluorescence quenching of fluorescein mercuric acetate in alkaline medium (1 n NaOH) was found to be an accurate, sensitive method for differential analysis of sulfhydryl and disulfide groups of intact bacterial spores. Disulfide content of three species of spores was found to be slightly higher than reported by other workers. A significant increase in sulfhydryl group concentration was observed after physiological germination, indicating participation of a disulfide-reducing system in the germination process.

Publisher

American Society for Microbiology

Subject

Molecular Biology,Microbiology

Reference10 articles.

1. Fluorimetry as a method of determining protein content of milk;HOLSINGER ND M;J. Dairy Sci.,1963

2. Development of fine structure, thermostability, and dipicolinate during sporogenesis in a Bacillus;HASHIMOTO T., S.;Can. J. Microbiol.,1960

3. HAUROWITZ F. 1963. The chemistry and function of proteins 2nd ed. p. 217 301. Academic Press Inc. New York.

4. The oxidation of ribonuclease with performic acid;W.;J. Biol. Chem.,1956

5. An assay method for disulfide groups by fluorescence quenching;KARUSH F., N.;Anal. Biochem.,1964

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