𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Expression of a β-galactosidase gene fromLactobacillus sakeinEscherichia coli

✍ Scribed by Maria J. Torres; Byong H. Lee


Publisher
Springer Netherlands
Year
1995
Tongue
English
Weight
415 KB
Volume
17
Category
Article
ISSN
0141-5492

No coin nor oath required. For personal study only.

✦ Synopsis


A B-galactosidase gene from Lactobacillus sake coding for lactose hydrolysis was cloned and expressed in Escherichia coli. Chromosomal DNA from L. 'sa& was partially digested with the restriction enzyme SaDAI, and the 3-6 Kb fragment was ligated to the cloning vector pSP72 digested with BarnHI. One E. coli transformant expressing B-galactosidase was isolated on X-gal plates. It contained a plasmid with an insertion of approx. 4 Kb. The restriction map of the recombinant plasmid was constructed. The characteristics of the recombinant B-galactosidase were compared with those of the wild type. The optima pH and temperature for both enzymes was 6.5 and 5O"C, respectively. Stability of the enzymes at different temperatures and activity on lactose were determined.


📜 SIMILAR VOLUMES


Cloning and expression of a glucoamylase
✍ Jennylynd A. James; Normand Robert; Byong H. Lee 📂 Article 📅 1996 🏛 Springer Netherlands 🌐 English ⚖ 457 KB

The glucoamylase gene from lactobacillus amylovorus was cloned and expressed in Escherichia coli. A genomic DNA library from Laclobacillus amylovorus was prepared by partially digesting genomic DNA with EC&I and ligating random fragments to the EcoRl digested cloning vector, pZErO-I .I. Three E. co/