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Preparation of GM1 ganglioside with sialidase-producing marine bacteria as a microbial biocatalyst.

机译:用产生唾液酸酶的海洋细菌作为微生物生物催化剂制备GM1神经节苷脂。

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摘要

This paper describes the preparation of monosialoganglioside GM1 with sialidase-producing marine bacteria as a microbial biocatalyst. A new sialidase-producing bacterium, identified tentatively as Pseudomonas sp. strain YF-2, was isolated from seawater by enrichment culture with ganglioside as the sole source of carbon. When YF-2 was cultured in a synthetic medium containing crude bovine brain gangliosides at 25 degrees C for 3 days, 80 to 90% of the gangliosides were converted to GM1. GM1 was then purified from the supernatant of YF-2 culture by C18 reverse-phased chromatography, followed by DEAE-Sephadex A25 anion-exchange chromatography. In a typical experiment, 178 mg of highly purified GM1 was obtained from 500 mg of the crude ganglioside fraction. The GM1 induced neurite outgrowth of neuroblastoma Neuro2a cells at a concentration of 33 to 100 microM in the presence of fetal calf serum. Sialidase was purified 33-fold with 13.3% recovery from the culture supernatant of YF-2. The purified enzyme hydrolyzed polysialogangliosides to produce GM1 but did not act on GM1. It was therefore concluded that polysialogangliosides in the culture of strain YF-2 were converted to GM1 by this sialidase.
机译:本文描述了用唾液酸酶产生的海洋细菌作为微生物生物催化剂制备单唾液酸神经节苷脂GM1。一种新的产生唾液酸酶的细菌,初步鉴定为假单胞菌属。通过用神经节苷脂作为唯一碳源的富集培养从海水中分离出菌株YF-2。当将YF-2在含有粗牛脑神经节苷脂的合成培养基中于25°C培养3天时,80%至90%的神经节苷脂被转化为GM1。然后通过C18反相色谱法,然后通过DEAE-Sephadex A25阴离子交换色谱法,从YF-2培养物的上清液中纯化GM1。在一个典型的实验中,从500 mg的神经节苷脂粗品级分中获得了178 mg高度纯化的GM1。在胎牛血清存在下,GM1以33至100 microM的浓度诱导神经母细胞瘤Neuro2a细胞的神经突生长。从YF-2的培养上清液中将唾液酸酶纯化33倍,回收率为13.3%。纯化的酶水解多唾液酸神经节苷脂产生GM1,但不作用于GM1。因此得出的结论是,该唾液酸酶将YF-2菌株培养物中的多唾液酸神经节苷脂转化为GM1。

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