Centre de Bioingénierie Gilbert Durand, U.M.R. C.N.R.S. 5504 and Laboratoire Associeé I.N.R.A., D.G.B.A., I.N.S.A., Complexe Scientifique de Rangueil, 31 077 Toulouse Cedex 4, France.
Appl Environ Microbiol. 1998 Apr;64(4):1298-302. doi: 10.1128/AEM.64.4.1298-1302.1998.
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% alpha(1-->2) linkages, while FGT catalyzes the synthesis of a linear dextran only composed of alpha(1-->6) linkages.
当在缺乏蔗糖的葡萄糖或果糖培养基中生长时,肠膜明串珠菌 NRRL B-1299 产生两种不同的细胞外葡聚糖蔗糖酶,分别命名为葡萄糖基转移酶 (GGT) 和果糖基转移酶 (FGT)。GGT 和 FGT 的产量比在蔗糖培养基(传统培养条件)上产生的细胞外葡聚糖蔗糖酶 (SGT) 低 10 到 20 倍。在进行十二烷基硫酸钠-聚丙烯酰胺凝胶电泳分析之前,通过超滤浓缩 GGT 和 FGT。它们的分子量分别为 183 和 186 kDa,与 SGT 的 195 kDa 不同。对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低聚糖的结构分析表明,GGT 和 FGT 是两种以前未描述过的该菌株的不同酶。由 GGT 合成的聚合物含有 30%的α(1-->2)键,而 FGT 仅催化由α(1-->6)键组成的线性葡聚糖的合成。