PURIFICATION AND SOME PROPERTIES OF ALPHA-AMYLASE FROM BACILLUS-SUBTILIS X-23 THAT GLUCOSYLATES PHENOLIC-COMPOUNDS SUCH AS HYDROQUINONE

被引:63
|
作者
NISHIMURA, T
KOMETANI, T
TAKII, H
TERADA, Y
OKADA, S
机构
[1] Biochemical Research Laboratory, Ezaki Glico Co. Ltd., Osaka, 555, 4-6-5 Utajima, Nishiyodogawa
来源
JOURNAL OF FERMENTATION AND BIOENGINEERING | 1994年 / 78卷 / 01期
关键词
D O I
10.1016/0922-338X(94)90174-0
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
Six hundred strains of soil microorganisms were screened for the production of hydroquinone glucosylating enzyme (HGE). One of these strains, Bacillus subtilis strain X-23, produced an enzyme that glucosylated hydroquinone in the culture filtrate. The HGE was successively purified by ammonium sulfate fractionation, and Q-Sepharose, Phenyl-Toyopearl, and Superose 12 column chromatographies. The molecular weight was estimated as 65 kDa by SDS-polyacrylamide gel electrophoresis, and 54 kDa by gel filtration. Based on an analysis of the hydrolytic products from soluble starch, HGE was considered to be a kind of alpha-amylase. The structure of the hydroquinone glucoside produced by HGE was identified as 4-hydroxyphenyl-O-alpha-D-glucopyranoside by alpha- and beta-glucosidase treatments, and H-1-NMR and C-13-NMR.
引用
收藏
页码:31 / 36
页数:6
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