黄色短杆菌

大肠杆菌pheA基因在黄色短杆菌中的克隆与表达

Cloning and Expressing of Escherichia coli Gene pheA in Brevibacterium flavum

大肠杆菌磷酸丝氨酸转氨酶基因的克隆和在黄色短杆菌中的表达

Cloning of Phosphoserine Aminotransferase Gene of Escherichia Coli and Expression in Brevibacterium Flavum

研究了用聚乙烯醇（PVA）包埋黄色短杆菌的固定化成型技术。

Shaping technique of immobilization was studied by using B.flavum cells entrapped in-to PVA .

絮凝方法收集产氨短杆菌MA-2、黄色短杆菌MA-3条件的优化

Optimization of flocculation conditions for collecting B. ammoniagenes MA-2 and B.flavum MA-3

提高黄色短杆菌C-11电转化效率的方法

Methods of increasing efficiency of electrotransformation of B.flavum C-11

黄色短杆菌GDK-9谷氨酸脱氢酶基因的克隆、序列分析及表达

Cloning , Sequence Analysis and Expression of Glutamate Dehydrogenase in Brevibacterium flavum GDK-9

采用壳聚糖作絮凝剂收集富含延胡索酸酶活力的产氨短杆菌MA2、黄色短杆菌MA3。

B. ammoniagenes MA 2 and B. flavum MA 3 were collected by using chitosan as flocculant .

无机凝聚剂氯化钙和高分子絮凝剂壳聚糖分别对富含延胡索酸酶的产氨短杆菌MA-2、黄色短杆菌MA-3进行凝聚和絮凝实验，两菌酶活回收率达959%～987%

The fumarase producing cells such as B.ammoniagenes MA-2 and B. flavum MA-3 were treated with inorganic coagulating reagent calcium chloride and high polymeric flocculating reagent chitosan respectively , and the recovery of the enzyme activity reached 95 9 % ~ 98 7 % .