Optimization of Isomaltooligosaccharide Size Distribution by Acceptor Reaction of Weissella confusa Dextransucrase and Characterization of Novel α-(1→2)-Branched Isomaltooligosaccharides
메타 데이터
바이오화학분류
바이오플라스틱
기타
바이오정밀화학
기타
화장품용 기능성소재
기타
의료용 화학소재
식품첨가제
논문
Optimization of Isomaltooligosaccharide Size Distribution by Acceptor Reaction of Weissella confusa Dextransucrase and Characterization of Novel α-(1→2)-Branched Isomaltooligosaccharides
<P>Long-chain isomaltooligosaccharides (IMOs) are promising prebiotics. IMOs were produced by a <I>Weissella confusa</I> dextransucrase via maltose acceptor reaction. The inputs of substrates (i.e., sucrose and maltose, 0.15–1 M) and dextransucrase (1–10 U/g sucrose) were used to control IMO yield and profile. According to response surface modeling, 1 M sucrose and 0.5 M maltose were optimal for the synthesis of longer IMOs, whereas the dextransucrase dosage showed no significant effect. In addition to the principal linear IMOs, a homologous series of minor IMOs were also produced from maltose. As identified by MS<SUP><I>n</I></SUP> and NMR spectroscopy, the minor trisaccharide contained an α-(1→2)-linked glucosyl residue on the reducing residue of maltose and thus was α-<SMALL>d</SMALL>-glucopyranosyl-(1→2)-[α-<SMALL>d</SMALL>-glucopyranosyl-(1→4)]-<SMALL>d</SMALL>-glucopyranose (centose). The higher members of the series were probably formed by the attachment of a single unit branch to linear IMOs. This is the first report of such α-(1→2)-branched IMOs produced from maltose by a dextransucrase.</P><P><B>Graphic Abstract</B><BR><IMG SRC='http://pubs.acs.org/appl/literatum/publisher/achs/journals/content/jafcau/2016/jafcau.2016.64.issue-16/acs.jafc.6b01356/production/images/medium/jf-2016-013568_0005.gif'></P><P><A href='http://pubs.acs.org/doi/suppl/10.1021/jf6b01356'>ACS Electronic Supporting Info</A></P>