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A new approach to determine the stereospecificity in lipase catalysed hydrolysis using circular dichroism (CD): lipases produce optically active diglycerides from achiral triglycerides.
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- Author(s): Uzawa H;Uzawa H; Nishida Y; Ohrui H; Meguro H
- Source:
Biochemical and biophysical research communications [Biochem Biophys Res Commun] 1990 Apr 30; Vol. 168 (2), pp. 506-11.
- Publication Type:
Journal Article
- Language:
English
- Additional Information
- Source:
Publisher: Elsevier Country of Publication: United States NLM ID: 0372516 Publication Model: Print Cited Medium: Print ISSN: 0006-291X (Print) Linking ISSN: 0006291X NLM ISO Abbreviation: Biochem Biophys Res Commun Subsets: MEDLINE
- Publication Information:
Publication: <2002- >: San Diego, CA : Elsevier
Original Publication: New York, Academic Press.
- Subject Terms:
- Abstract:
We describe a sensitive CD method for determining the stereospecificity in lipase (E.C.3.1.1.3) catalysed hydrolysis of triacyl glycerols into diacyl glycerols. The diglycerols were converted to chiral tert-butyldimethylsilylated 1,2- or 2,3-di-O-benzoyl-sn-glycerol (5 or 5'), and their CD was measured. This approach showed for the first time that lipases produce optically active diacyl glycerides from achiral tripalmitin and tribenzoyl glyceride with a variable extent of enantioselectivity depending on the acyl groups and the enzymes.
- Accession Number:
0 (Benzyl Alcohols)
0 (Diglycerides)
0 (Glycerides)
0 (Triglycerides)
EC 3.1.1.3 (Lipase)
- Publication Date:
Date Created: 19900430 Date Completed: 19900604 Latest Revision: 20190612
- Publication Date:
20221213
- Accession Number:
10.1016/0006-291x(90)92350-9
- Accession Number:
2334421
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