Literature DB >> 6346947

An enzymatic assay for acetate in spent bacterial culture supernatants.

P M Clarke, M A Payton.   

Abstract

A method is presented for the rapid enzymatic determination of acetate in spent bacterial culture supernatants. The assay is based on a previously published assay for acetate kinase [Bergmeyer et al. (1974) in Methods of Enzymatic Analysis (Bergmeyer, H. V., ed.), Vol. 1, pp. 425-426, Verlag Chemie-Academic Press, New York/London], and is sufficiently sensitive to detect acetate levels of 50 microM. The assay is cheaper than commercially available assays and is particularly useful for occasional use by laboratories not equipped for routine acetate analysis using gas chromatography. The application of the assay to the measurement of acetate in bacterial cultures is described, though it should also be applicable to other biological fluids and foodstuffs.

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Year:  1983        PMID: 6346947     DOI: 10.1016/0003-2697(83)90607-3

Source DB:  PubMed          Journal:  Anal Biochem        ISSN: 0003-2697            Impact factor:   3.365


  2 in total

1.  Direct detection of the acetate-forming activity of the enzyme acetate kinase.

Authors:  Matthew L Fowler; Cheryl J Ingram-Smith; Kerry S Smith
Journal:  J Vis Exp       Date:  2011-12-19       Impact factor: 1.355

2.  RpiR homologues may link Staphylococcus aureus RNAIII synthesis and pentose phosphate pathway regulation.

Authors:  Yefei Zhu; Renu Nandakumar; Marat R Sadykov; Nandakumar Madayiputhiya; Thanh T Luong; Rosmarie Gaupp; Chia Y Lee; Greg A Somerville
Journal:  J Bacteriol       Date:  2011-09-16       Impact factor: 3.490

  2 in total

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