Process for producing high purity 6, 12-dideoxyerythromycin A by

Chemistry: molecular biology and microbiology – Micro-organism – tissue cell culture or enzyme using process... – Preparing compound containing saccharide radical

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4351721, 4351723, 4352523, 43525233, 43525411, 43525421, 4353201, 514 29, 536 72, 536 231, C12P 1962

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057861811

ABSTRACT:
A process for producing high purity 6,12-dideoxyerythromycin A using recombinant DNA technology is disclosed. The erythromycin producing strain, Saccharopolyspora erythraea, lacking the erythromycin C-12 and C-6 hydroxylases produces a mixture of 6,12-dideoxyerythromycin A and the precursor molecule, 6-deoxyerythromycin D. To achieve conversion of the precursor to the final product, a second copy of eryG is inserted into a non-essential region of the Sac. erythraea chromosome resulting in high purity 6,12-dideoxyerythromycin A.

REFERENCES:
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Gene, vol. 75 (1989), pp. 235-241, J. M. Weber, et al., "Identification of a Gene Required for the Terminal Step in Erythromycin A Biosynthesis in Saccharopolyspora Erythraea (Streptomyces erythreus)".
Journal of Bacteriology, vol. 175, No. 1, (Jan. 1993), pp. 182-189, D. Stassi, et al., "Identification of a Saccharopolyspora erythraea Gene Required for the Final Hydroxylation Step in Erythromycin Biosynthesis".
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