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固定在海藻酸钙凝胶中的谷氨酸棒杆菌T6-13原生质体产生细胞内酶。

Production of intracellular enzyme by Corynebacterium glutamicum T6-13 protoplasts immobilized in Ca-alginate gels.

作者信息

Su Z, Guo Y, Peng Z

机构信息

Institute of Biotechnology, South China University of Technology, Guangzhou.

出版信息

Enzyme Microb Technol. 1993 Sep;15(9):791-5. doi: 10.1016/0141-0229(93)90011-p.

Abstract

The glutamate dehydrogenase (GDH) (EC 1.4.1.4) productivity of the immobilized Corynebacterium glutamicum T6-13 protoplasts in Ca-alginate gels was investigated. GDH in Corynebacterium glutamicum T6-13 cells is an intracellular enzyme. The cells pretreated with 0.5 U/l-1 penicillin G were used for the preparation of protoplasts. Protoplasts were prepared by treating these cells with lysozyme at 30 degrees C for 14 h in 0.5 M NaCl solution and separating the protoplasts. Protoplasts were directly immobilized in 3% Ca-alginate gels (method I). The immobilized protoplasts could be also prepared by treating the immobilized whole cells with lysozyme (method II); this method was more convenient than method I. The GDH productivity of the immobilized protoplasts amounted to 205% of that of the free cells (intracellular). The immobilized protoplasts could be repeatedly used for at least 6 batches (18 days) and had good storage stability.

摘要

研究了固定在海藻酸钙凝胶中的谷氨酸棒杆菌T6-13原生质体的谷氨酸脱氢酶(GDH)(EC 1.4.1.4)生产能力。谷氨酸棒杆菌T6-13细胞中的GDH是一种胞内酶。用0.5 U/l-1青霉素G预处理的细胞用于制备原生质体。通过在0.5 M NaCl溶液中于30℃用溶菌酶处理这些细胞14小时并分离原生质体来制备原生质体。原生质体直接固定在3%海藻酸钙凝胶中(方法I)。固定化原生质体也可以通过用溶菌酶处理固定化的完整细胞来制备(方法II);该方法比方法I更方便。固定化原生质体的GDH生产能力相当于游离细胞(胞内)的205%。固定化原生质体可以重复使用至少6批(18天),并且具有良好的储存稳定性。

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