The use of Pseudomonas acyl-CoA synthetase to form acyl-CoAs from dicarboxylic fatty acids

Kenneth G. Milne, Angela Mehlert, Michael A. J. Ferguson

    Research output: Contribution to journalArticle

    2 Citations (Scopus)

    Abstract

    Pseudomonas acyl-CoA synthetase is shown to act on saturated dicarboxylic acids with a chain length of C10 or greater to produce conjugates containing a single CoA unit. The synthetase can, therefore, be used to generate novel acyl-CoA analogues for studies on proteins that utilise, bind to, or are modulated by acyl-CoAs. (C) 2001 Elsevier Science B.V. All rights reserved.

    Original languageEnglish
    Pages (from-to)1-3
    Number of pages3
    JournalBiochimica et Biophysica Acta-Molecular and Cell Biology of Lipids
    Volume1531
    Issue number1-2
    DOIs
    Publication statusPublished - 30 Mar 2001

    Cite this

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    title = "The use of Pseudomonas acyl-CoA synthetase to form acyl-CoAs from dicarboxylic fatty acids",
    abstract = "Pseudomonas acyl-CoA synthetase is shown to act on saturated dicarboxylic acids with a chain length of C10 or greater to produce conjugates containing a single CoA unit. The synthetase can, therefore, be used to generate novel acyl-CoA analogues for studies on proteins that utilise, bind to, or are modulated by acyl-CoAs. (C) 2001 Elsevier Science B.V. All rights reserved.",
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    The use of Pseudomonas acyl-CoA synthetase to form acyl-CoAs from dicarboxylic fatty acids. / Milne, Kenneth G. ; Mehlert, Angela ; Ferguson, Michael A. J. .

    In: Biochimica et Biophysica Acta-Molecular and Cell Biology of Lipids, Vol. 1531, No. 1-2, 30.03.2001, p. 1-3.

    Research output: Contribution to journalArticle

    TY - JOUR

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    AU - Milne, Kenneth G.

    AU - Mehlert, Angela

    AU - Ferguson, Michael A. J.

    PY - 2001/3/30

    Y1 - 2001/3/30

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    AB - Pseudomonas acyl-CoA synthetase is shown to act on saturated dicarboxylic acids with a chain length of C10 or greater to produce conjugates containing a single CoA unit. The synthetase can, therefore, be used to generate novel acyl-CoA analogues for studies on proteins that utilise, bind to, or are modulated by acyl-CoAs. (C) 2001 Elsevier Science B.V. All rights reserved.

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    JO - Biochimica et Biophysica Acta-Molecular and Cell Biology of Lipids

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