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Heparinase production by Flavobacterium heparinum.

机译:肝黄杆菌生产肝素酶。

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Heparinase production by Flavobacterium heparinum in complex protein digest medium, with heparin employed as the inducer, has been studied and improved. The maximum productivity of heparinase has been increased 156-fold over that achieved by previously published methods to 375 U/liter per h in the complex medium. Rapid deactivation of heparinase activity, both specific and total, was observed at the onset of the stationary phase. Nutritional studies on growth and heparinase production showed an obligate requirement for L-histidine and no vitamin requirement. L-Methionine partially relieved the L-histidine requirement. A defined medium containing glucose, ammonium sulfate, basal salts, L-methionine, and L-histidine was developed for growth and heparinase production. The growth rate in this medium was 0.21 h-1, which is 40%, higher than that in complex medium. The maximum volumetric productivity of heparinase in the defined medium was increased to 1,475 U/liter per h, providing a 640-fold increase over that achieved by previously published methods. No rapid deactivation was observed. An examination of alternate inducers for heparinase showed that heparin degradation products, hyaluronic acid, heparin monosulfate, N-acetyl-D-glucosamine, and maltose, induce heparinase in complex medium. An Azure A assay was modified and fully developed to measure the heparin concentration during fermentation and the heparinase specific activity of crude extracts of F. heparinum obtained from sonication, thus negating the need for further purification to measure activity."
机译:已经研究并改进了肝黄杆菌在复杂蛋白消化培养基中以肝素为诱导剂生产肝素酶的方法。在复杂培养基中,肝素酶的最大生产率比以前公布的方法提高了156倍,达到每小时375 U /升。在固定相开始时观察到肝素酶活性的快速失活,无论是特异性的还是全部的。关于生长和肝素酶生产的营养研究表明,对L-组氨酸的需要量是绝对的,而对维生素的需求却不多。 L-蛋氨酸可部分缓解L-组氨酸的需求。开发了包含葡萄糖,硫酸铵,基础盐,L-蛋氨酸和L-组氨酸的确定培养基,用于生长和肝素酶生产。该培养基的生长速率为0.21 h-1,比复合培养基高40%。在定义的培养基中,肝素酶的最大体积生产率提高到每小时1,475 U /升,比以前公布的方法提高了640倍。没有观察到快速失活。对肝素酶替代诱导剂的检查表明,肝素降解产物,透明质酸,肝素单硫酸盐,N-乙酰基-D-葡萄糖胺和麦芽糖可在复杂培养基中诱导肝素酶。修改并充分开发了Azure A测定法,以测量发酵过程中的肝素浓度和超声处理得到的肝炎肝菌粗提物的肝素酶比活性,因此无需进一步纯化以测定活性。”

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