Takada K, Shiota T, Ikeda T
Department of Microbiology, Nihon University School of Dentistry, Matsudo, Chiba, Japan.
Biochim Biophys Acta. 1990 Jan 29;1033(1):91-5. doi: 10.1016/0304-4165(90)90199-7.
Culture supernatant fluids (SF) of mutant 108 obtained from Streptococcus sobrinus 6715, when incubated with sucrose, produce large amounts of water-soluble glucans. Mainly, two water-soluble glucan synthesizing glucosyltransferases (GTases) were found in culture SF by isoelectric focusing. These two GTases had higher activities than those from the parent strain. The GTase which synthesizes water-insoluble glucan totally lacked the mutant. When the glucan preparation synthesized by the SF was subjected to gel filtration, a major large molecular weight fraction (designated glucan A) and a small molecular weight fraction (designated glucan B) were obtained. Glucan A yielded a smaller molecular weight glucan after treatment with dextranase. Glucan B was not hydrolyzed by the same enzyme.
从远缘链球菌6715获得的突变体108的培养上清液(SF)与蔗糖一起孵育时,会产生大量水溶性葡聚糖。通过等电聚焦在培养SF中主要发现了两种合成水溶性葡聚糖的葡糖基转移酶(GTases)。这两种GTases的活性高于亲本菌株的。合成水不溶性葡聚糖的GTase在该突变体中完全缺失。当由SF合成的葡聚糖制剂进行凝胶过滤时,得到一个主要的大分子量级分(称为葡聚糖A)和一个小分子量级分(称为葡聚糖B)。用葡聚糖酶处理后,葡聚糖A产生分子量较小的葡聚糖。相同的酶不会水解葡聚糖B。