원문정보
Improvement of Insoluble B-Glucosidase Activity by Molecular Chaperonin GroEL/ES
초록
영어
B-Glucosidaes from Cellvibrio gilvus(CG) was successfully overproduced in soluble form in E. coli with the coexpression of GroEL/ES/. Without the GroEL/ES protein, the B-glucosidase overexpressed in E. coli constituted a huge amount(80%) of total cellular protein, but was localized in the insoluble fraction, and little activity was detected in the soluble fraction. Coexpression of the E. coli GroEL/ES had a drastic impact on the proper folding of the B-glucosidase; 20% of the overexpressed enzyme was recovered in the soluble fraction in active form. Similar effects of GroEL/ES were also observed on the overexpressed -glucosidase from Agrobacterium tumefaciens(AT). And pET28(a)-RGRAR, partially deleted mutant lacking 5-amino acid residues at carboxy teminus also could be folded into an active form when expressed with the molecular chaperonin GroEL/ES, and its activity was higher than that of the without GroEL/ES system, In addition, the synergistic effect of GroEL/ES and the low induction temperature were important factors for solubilization of the inclusion body from overproduced -glucosidases.
목차
재료 및 방법
Bacterial strain and vectors
배지
GroEL/ES system
균체의 배양
SDS-PAGE
결과 및 고찰
균주의 성장
E. coli 내에서의 B-glucosidase의 과잉 생산
단백질의 과잉생산 및 chaperonin에 의한 가용화
Chaperonin에 의한 B-glucosidase의 총 활성의 향상
저온 배양에 따른 B -glucosidase의 가용성 향상
Coexpression과 저온 배양의 synergic effect
Deleted mutant의 chaperonin에 의한 총 활성의 향상
결론
참고문헌
