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<!DOCTYPE ArticleSet PUBLIC "-//NLM//DTD PubMed 2.0//EN" "http://www.ncbi.nlm.nih.gov:80/entrez/query/static/PubMed.dtd">
<ArticleSet>
<Article>
<Journal>
<PublisherName>Science and Education Publishing</PublisherName>
<JournalTitle>Journal of Food and Nutrition Research</JournalTitle>
<Issn>2333-1240</Issn>
<Volume>2</Volume>
<Issue>4</Issue>
<PubDate PubStatus="epublish">
<Year>2014</Year>
<Month>05</Month>
<Day>14</Day>
</PubDate>
</Journal>
<ArticleTitle>Biosynthesis of 2-O-α-D-glucopyranosyl-L-Ascorbic Acid from Maltose by Cyclodextrin Glucanotransferase from Bacillus sp. SK 13.002</ArticleTitle>
<FirstPage>193</FirstPage>
<LastPage>197</LastPage>
<Language>EN</Language>
<AuthorList>
<Author>
<FirstName>Ahmed</FirstName>
<LastName>Eibaid</LastName>
</Author>
<Author>
<FirstName>Mohanad</FirstName>
<LastName>Bashari</LastName>
</Author>
<Author>
<FirstName>Ming</FirstName>
<LastName>Miao</LastName>
</Author>
<Author>
<FirstName>Abubakr</FirstName>
<LastName>Musa</LastName>
</Author>
<Author>
<FirstName>Tao</FirstName>
<LastName>Zhang</LastName>
</Author>
<Author>
<FirstName>Bo</FirstName>
<LastName>Jiang</LastName>
<Affiliation>State Key Laboratory of Food Science and Technology, Synergetic Innovation Center of Food Safety and Nutrition, Jiangnan University, Wuxi, China</Affiliation>
</Author>

</AuthorList>
<ArticleIdList>
<ArticleId IdType="pii">JFNR20142410</ArticleId>
<ArticleId IdType="doi">10.12691/jfnr-2-4-10</ArticleId>
</ArticleIdList>
<History>
<PubDate PubStatus="received">
<Year>2014</Year>
<Month>04</Month>
<Day>11</Day>
</PubDate>
<PubDate PubStatus="revised">
<Year>2014</Year>
<Month>05</Month>
<Day>12</Day>
</PubDate>
<PubDate PubStatus="accepted">
<Year>2014</Year>
<Month>05</Month>
<Day>14</Day>
</PubDate>
</History>
<Abstract>In this work 2-O-α-D-glucopyranosyl-L-ascorbic acid (AA-2G) was synthesized by Cyclodextrin glucanotransferase (CGTase) from Bacillus sp. SK 13.002 with L-ascorbic acid (AA) as an acceptor and maltose as a glycosyl donor. AA-2G production was analyzed by HPLC and was confirmed by LC/MS results. The reaction parameters, such as pH (4.0-9.0), temperature (25-50C), time (0-30 h), substrate ratios and enzyme concentration were optimized. The results showed that the optimum condition was pH 8.0 at 37C for 24 h, 1:1 maltose to AA substrates mass ratio, and 200 U/mL of CGTase. Under these conditions, the production of AA-2G was 5.5 g/L, this result indicate that CGTase from Bacillus sp. SK 13.002 can effectively uses maltose as a glycosyl donor to produce AA-2G in high yield.</Abstract>
</Article>
</ArticleSet>
