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Genetic dissection of the biosynthetic route to gentamicin A2 by heterologous expression of its minimal gene set

Genetic dissection of the biosynthetic route to gentamicin A2 by heterologous expression of its minimal gene set
Je W.P.Hong J.S.J.Parajuli N.Won S.J.Sung R.P.Lim S.-K.Jae K.S.Yeo J.Y.
Ewha Authors
Issue Date
Journal Title
Proceedings of the National Academy of Sciences of the United States of America
0027-8424JCR Link
vol. 105, no. 24, pp. 8399 - 8404
Since the first use of streptomycin as an effective antibiotic drug in the treatment of tuberculosis, aminoglycoside antibiotics have been widely used against a variety of bacterial infections for over six decades. However, the pathways for aminoglycoside biosynthesis still remain unclear, mainly because of difficulty in genetic manipulation of actinomycetes producing this class of antibiotics. Gentamicin belongs to the group of 4,6-disubstituted aminoglycosides containing a characteristic core aminocyclitol moiety, 2-deoxystreptamine (2-DOS), and the recent discovery of its biosynthetic gene cluster in Micromonospora echinospora has enabled us to decipher its biosynthetic pathway. To determine the minimal set of genes and their functions for the generation of gentamicin A2, the first pseudotrisaccharide intermediate in the biosynthetic pathway for the gentamicin complex, various sets of candidate genes from M. echinospora and other related aminoglycoside-producing strains were introduced into a nonaminoglycoside producing strain of Streptomyces venezuelae. Heterologous expression of different combinations of putative 2-DOS biosynthetic genes revealed that a subset, gtmB-gtmA-gacH, is responsible for the biosynthesis of this core aminocyclitol moiety of gentamicin. Expression of gtmG together with gtmB-gtmA-gacH led to production of 2′-N-acetylparomamine, demonstrating that GtmG acts as a glycosyltransferase that adds N-acetyl-D-glucosamine (GLcNA) to 2-DOS. Expression of gtmM in a 2′-N-acetylparomamine-producing recombinant S. venezuelae strain generated paromamine. Expression of gtmE in an engineered paromamine-producing strain of S. venezuelae successfully generated gentamicin A2, indicating that GtmE is another glycosyltransferase that attaches D-xylose to paromamine. These results represent in vivo evidence elucidating the complete biosynthetic pathway of the pseudotrisaccharide aminoglycoside. © 2008 by The National Academy of Sciences of the USA.
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