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用于产谷氨酸细菌乳酸发酵短杆菌和谷氨酸棒杆菌的新型穿梭载体和黏粒载体的构建。

Construction of novel shuttle vectors and a cosmid vector for the glutamic acid-producing bacteria Brevibacterium lactofermentum and Corynebacterium glutamicum.

作者信息

Miwa K, Matsui K, Terabe M, Ito K, Ishida M, Takagi H, Nakamori S, Sano K

出版信息

Gene. 1985;39(2-3):281-6. doi: 10.1016/0378-1119(85)90324-5.

Abstract

Novel cloning vectors for glutamic acid-producing bacteria have been constructed. Two cryptic plasmids, pAM330 from Brevibacterium lactofermentum and pHM1519 from Corynebacterium glutamicum, were used as precursors, and recombined with pBR325 or pUB110. Resultant composite plasmids were able to propagate and to express the CmR or KmR phenotype in B. lactofermentum and C. glutamicum. A smaller, high-copy-number plasmid, pAJ43, was also isolated following deletion of a part of the pAM330-pBR325 composite plasmid. Furthermore, a cosmid vector, which can be packaged and transduced through phage infection, has been developed using a cohesive-end fragment of the f1A phage and plasmid pAJ43. These plasmids are suitable for use as cloning vectors in the glutamic acid-producing bacteria.

摘要

已构建出用于谷氨酸生产菌的新型克隆载体。使用了两种隐蔽质粒,来自乳酸发酵短杆菌的pAM330和来自谷氨酸棒杆菌的pHM1519作为前体,并与pBR325或pUB110进行重组。所得的复合质粒能够在乳酸发酵短杆菌和谷氨酸棒杆菌中复制并表达CmR或KmR表型。在删除部分pAM330 - pBR325复合质粒后,还分离出了一个较小的高拷贝数质粒pAJ43。此外,利用f1A噬菌体的粘性末端片段和质粒pAJ43开发了一种可通过噬菌体感染进行包装和转导的粘粒载体。这些质粒适合用作谷氨酸生产菌中的克隆载体。

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