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Updated: Apr 16, 2026

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A Facile Protocol to Generate Site-Specifically Acetylated Proteins in Escherichia Coli
Published on: December 9, 2017
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[Expression of acylamidase gene in Rhodococcus erythropolis strains]
Genetika
|March 5, 2015
Summary
Researchers developed a novel expression system for Rhodococcus erythropolis, enhancing acylamidase production. This system significantly boosts acylamidase activity in recombinant strains for improved industrial applications.
Area of Science:
- Microbiology and Molecular Biology
- Enzyme Engineering
- Biotechnology
Context:
- Studying acylamidase gene expression in Rhodococcus erythropolis strains.
- Characterizing a novel acylamidase with unique substrate specificity for N-substituted amides.
- Developing efficient expression systems for microbial hosts.
Purpose:
- To create a novel expression system for constitutive acylamidase synthesis in R. erythropolis.
- To enhance the production of a specific acylamidase enzyme.
- To improve the efficiency of biocatalysis using recombinant microorganisms.
Summary:
- A new expression system utilizing the promoter region of nitrilhydratase genes from R. rhodochrous M8 was constructed for R. erythropolis.
- This system enabled constitutive synthesis of a novel acylamidase from R. erythropolis 37.
- Recombinant R. erythropolis cells exhibited a fourfold increase in acylamidase activity compared to the wild-type strain.
Impact:
- Facilitates enhanced production of acylamidase for potential industrial biocatalysis.
- Demonstrates a successful strategy for improving enzyme expression in Rhodococcus species.
- Opens avenues for metabolic engineering of R. erythropolis for specific enzymatic applications.

