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Determination of mannuronan C-5-epimerase activity in fermentation broth of Azotobacter vinelandii
被引:5
|作者:
Ramstad, MV
[1
]
Elingsen, TE
[1
]
Levine, DW
[1
]
机构:
[1] UNIV TRONDHEIM,NORWEGIAN INST TECHNOL,DEPT BIOTECHNOL,N-7034 TRONDHEIM,NORWAY
关键词:
mannuronan C-5-epimerase;
Azotobacter vinelandii;
radioactive assay;
H-3]-alginate;
D O I:
10.1016/S0141-0229(96)00146-9
中图分类号:
Q81 [生物工程学(生物技术)];
Q93 [微生物学];
学科分类号:
071005 ;
0836 ;
090102 ;
100705 ;
摘要:
Azotobacter vinelandii produces extracellular mannuronan C-5-epimerase activity. This activity appears during the biosynthesis of alginate and converts D-mannuronic acid residues into L-guluronic acid in the polymer chain. In order to study the production of mannuronan C-5-epimerase by fermentation of A. vinelandii, a rapid and reproducible assay for the analysis of epimerase activity in the fermentation broth is required. We have examined a method in which [H-3]-alginate is used as a substrate and the tritium released into water is measured. Fermentation broths contain compounds and ions which may interfere with the analysis or affect the activity of the enzyme. The effects of potential interfering compounds have been characterized and the uncertainty of the analysis system has been determined. Furthermore, a standard method suitable for use directly on the fermentation broth has been developed. The standard deviation of this method within a single analysis is +/-2.5% whereas the standard deviation for samples measured several times in separate analyses on the average is 10%. (C) 1997 by Elsevier Science Inc.
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页码:308 / 316
页数:9
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