Engineering Antibiotic Producers to Overcome the Limitations of Classical Strain Improvement Programs-Reference-Cited by-同舟云学术

Engineering Antibiotic Producers to Overcome the Limitations of Classical Strain Improvement Programs

Published:1996-01 Issue:4 Volume:22 Page:201-255
ISSN:1040-841X
Container-title:Critical Reviews in Microbiology
language:en
Short-container-title:Critical Reviews in Microbiology

Author:

Lal Rup,Khanna Richie,Kaur Hardeep,Khanna Monisha,Dhingra Nidhi,Lal Sukanya,Gartemann Karl-Heinz,Eichenlaub Rudolf,Ghosh P. K.

Publisher

Informa UK Limited

Subject

Applied Microbiology and Biotechnology,General Medicine,Microbiology

Link

http://www.tandfonline.com/doi/pdf/10.3109/10408419609105481

Reference218 articles.

1. Ghosh P. K. Biotechnology Industries in India: Investment Opportunities, Industrial Biotechnology, V. S. Malick, P. Sridhar. Oxford IBT, New Delhi 1992; 71

2. Ghisalba Auden O., Schupp J. A. L.T., Nusch J. The rifamycins: properties, biosynthesis and fermentation. Biotechnology of Industrial Antibiotics. 1984; 282

3. A genetic approach to the biosynthesis of the Rifamycin-chromophore in Nocardia mediterranei. III. Isolation and identification of an early aromatic ansamycin-precursor containing the seven-carbon amino starter-unit and three initial acetate/propionate-units of the ansa chain.

4. Transformation of rifamycin S into rifamycins B and L. A revision of the current biosynthetic hypothesis.

5. Early intermediates in the biosynthesis of ansamycins. II. Isolation and identification of proasamycin B-M1 and protorifamycin I-M1.

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