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链球菌唾液酸酶。I. K组链球菌产生的唾液酸酶的分离及性质

Streptococcal sialidase. I. Isolation and properties of sialidase produced by group K Streptococcus.

作者信息

Hayano S, Tanaka A

出版信息

J Bacteriol. 1967 Jun;93(6):1753-7. doi: 10.1128/jb.93.6.1753-1757.1967.

Abstract

A survey has been made of the activity of a wide variety of standard strains of streptococci against bovine submaxillary mucin. Strain 6646 (group K) and strain D 168A "X" (group M) completely broke down and strain H 60R (group F) incompletely broke down bound sialic acid of bovine submaxillary mucin added to the growth medium. Among these strains, strain 6646 (group K) produced sialidase in the cell and in the culture fluid. An appropriate amount of glucose in the culture medium stimulated growth and the production of enzyme, but an excess of glucose in the culture medium caused abundant growth without production of the enzyme. The streptococcal sialidase was precipitated from the culture fluid by ammonium sulfate at 50% saturation, and further purification was achieved by diethylaminoethyl cellulose chromatography. Ca(++) and Co(++) stimulated the sialidase activity, and Mn(++), Zn(++), and ethylenediaminetetraacetate inhibited it. With acetate buffer, the optimal pH lay between 5 and 6. Sialic acid was detected in the reaction product of the streptococcal sialidase and bovine submaxillary mucin.

摘要

对多种标准链球菌菌株针对牛颌下粘蛋白的活性进行了一项调查。6646菌株(K组)和D 168A“X”菌株(M组)能完全分解,而H 60R菌株(F组)能不完全分解添加到生长培养基中的牛颌下粘蛋白的结合唾液酸。在这些菌株中,6646菌株(K组)在细胞内和培养液中产生唾液酸酶。培养基中适量的葡萄糖刺激生长和酶的产生,但培养基中过量的葡萄糖会导致大量生长而不产生酶。链球菌唾液酸酶在50%饱和度的硫酸铵作用下从培养液中沉淀出来,并通过二乙氨基乙基纤维素色谱法进一步纯化。Ca(++)和Co(++)刺激唾液酸酶活性,而Mn(++)、Zn(++)和乙二胺四乙酸抑制其活性。对于醋酸盐缓冲液,最佳pH值在5至6之间。在链球菌唾液酸酶与牛颌下粘蛋白的反应产物中检测到了唾液酸。

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