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9
Cloning and expression in Escherichia coli of the gene encoding the Proteus vulgaris chondroitin ABC lyase.普通变形杆菌软骨素ABC裂解酶编码基因在大肠杆菌中的克隆与表达。
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Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
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Identification of Pseudomonas pyocyanea by the oxidase reaction.通过氧化酶反应鉴定绿脓杆菌。
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The mucopolysaccharides of bovine cornea.牛角膜的黏多糖
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The taxonomic significance of fermentative versus oxidative metabolism of carbohydrates by various gram negative bacteria.各种革兰氏阴性菌对碳水化合物的发酵代谢与氧化代谢的分类学意义。
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Partial purification and characterization of chondroitinase from Proteus mirabilis.
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8
Purification and properties of bacterial chondroitinases and chondrosulfatases.细菌软骨素酶和软骨素硫酸酯酶的纯化及性质
J Biol Chem. 1968 Apr 10;243(7):1523-35.
9
Rapid plate method for screening hyaluronidase and chondroitin sulfatase-producing microorganisms.用于筛选产生透明质酸酶和硫酸软骨素酶的微生物的快速平板法
Appl Microbiol. 1968 Sep;16(9):1434-6. doi: 10.1128/am.16.9.1434-1436.1968.

Chondroitinase-producing bacteria in natural habitats.

作者信息

Kitamikado M, Lee Y Z

出版信息

Appl Microbiol. 1975 Mar;29(3):414-21. doi: 10.1128/am.29.3.414-421.1975.

DOI:10.1128/am.29.3.414-421.1975
PMID:803822
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC186989/
Abstract

A search was undertaken for bacteria which degrade chondroitin sulfate in nature and to find bacteria with a usefully high rate of chondroitinase (ChSase) productivity. First, 253 ChSase-producing bacteria were obtained from aquatic and land environments in Japan by aerobic and anaerobic screening methods. Identification according to Bergey's Manual of Determinative Bacteriology or Bain and Shewan (1968) permitted assignment of the majority of the isolates to seven genera, Aeromonas, Vibrio, Flavobacterium, Beneckea, Proteus, Micrococcus, and Arthrobacter. Next, ChSase productivities of all the isolates were compared with those of two established ChSase-producing stock strains, Proteus vulgaris NCTC 4636 and Flavobacterium heparinum ATCC 13125. As a result, special attention was given to production by a strain of Aeromonas sp. of large quantities of extracellular ChSase-AC. None of the isolates from the current study displayed significant ChSase-ABC productivity. Finally, ChSase-AC was prepared from the culture fluid of the Aeromonas strain by fractional precipitation with ammonium sulfate, chromatography on phospho-cellulose and diethylaminoethyl-cellulose, and gel filtration on Sephadex G-200. It was concluded that the Aeromonas strain may represent a profitable source of the enzyme ChSase-AC.

摘要