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Characterization of the Different Dextransucrase Activities Excreted in Glucose Fructose or Sucrose Medium by Leuconostoc mesenteroides NRRL B-1299

机译:mesenteroides NRRL B-1299在葡萄糖果糖或蔗糖培养基中分泌的不同右旋糖核酸酶活性的表征

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摘要

When grown in glucose or fructose medium in the absence of sucrose, Leuconostoc mesenteroides NRRL B-1299 produces two distinct extracellular dextransucrases named glucose glucosyltransferase (GGT) and fructose glucosyltransferase (FGT). The production level of GGT and FGT is 10 to 20 times lower than that of the extracellular dextransucrase sucrose glucosyltransferase (SGT) produced on sucrose medium (traditional culture conditions). GGT and FGT were concentrated by ultrafiltration before sodium dodecyl sulfate-polyacrylamide gel electrophoresis analysis. Their molecular masses were 183 and 186 kDa, respectively, differing from the 195 kDa of SGT. The structural analysis of the dextran produced from sucrose and of the oligosaccharides synthesized by acceptor reaction in the presence of maltose showed that GGT and FGT are two different enzymes not previously described for this strain. The polymer synthesized by GGT contains 30% α(1→2) linkages, while FGT catalyzes the synthesis of a linear dextran only composed of α(1→6) linkages.
机译:当在不存在蔗糖的情况下在葡萄糖或果糖培养基中生长时,肠膜肠球菌NRNR B-1299会产生两种不同的细胞外葡聚糖转移酶,分别称为葡萄糖葡糖基转移酶(GGT)和果糖葡糖基转移酶(FGT)。 GGT和FGT的生产水平比在蔗糖培养基上(传统培养条件)生产的细胞外葡糖转糖酶蔗糖葡萄糖基转移酶(SGT)低10到20倍。通过十二烷基硫酸钠-聚丙烯酰胺凝胶电泳前的超滤浓缩GGT和FGT。它们的分子量分别为183 kDa和186 kDa,与SGT的195 kDa不同。由蔗糖产生的葡聚糖和在麦芽糖存在下通过受体反应合成的寡糖的结构分析表明,GGT和FGT是该菌株先前未描述的两种不同的酶。由GGT合成的聚合物包含30%的α(1→2)键,而FGT催化仅由α(1→6)键组成的线性葡聚糖的合成。

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