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[从一株高产糖化酶菌株中分离和测序糖化酶基因]

[Isolation and sequencing of glucoamylase gene from a glucoamylase over producing strain].

作者信息

Zhong L, Tang G, Yang K

机构信息

Institute of Microbiology Academia Sinica, Beijing.

出版信息

Wei Sheng Wu Xue Bao. 1994 Jun;34(3):184-90.

PMID:7975554
Abstract

Chromosomal DNA was isolated from the mycelia of Aspergillus niger T21, a strain producing glucoamylase at a high level. Southern blot analysis indicated that the glucoamylase gene is situated on a 2.5kb EcoR I -EcoR V fragment. Chromosomal DNA was digested completely with EcoR I, EcoR V. The fragments in the range of 2.0-3.0kb were isolated through electrophoresis in agarose gel. The pooled fragments were ligated onto pBR322 vector prior to transformation into E. coli DH5. Four glucoamylase-specific recombinants were screened by in situ hybridization from the transformants. Restriction mapping and sequencing for one of the four were performed. Data show that the glucoamylase gene from A. niger T21 is a 2.3kb fragment containing four intervening sequences in the coding region.

摘要

从高产糖化酶的黑曲霉T21菌株的菌丝体中分离出染色体DNA。Southern杂交分析表明,糖化酶基因位于一个2.5kb的EcoR I -EcoR V片段上。用EcoR I和EcoR V完全消化染色体DNA。通过琼脂糖凝胶电泳分离出2.0 - 3.0kb范围内的片段。在转化到大肠杆菌DH5之前,将合并的片段连接到pBR322载体上。通过原位杂交从转化体中筛选出四个糖化酶特异性重组体。对这四个重组体中的一个进行了限制性图谱分析和测序。数据表明,黑曲霉T21的糖化酶基因是一个2.3kb的片段,在编码区含有四个间隔序列。

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