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Science 9 January 1998: Vol. 279. no. 5348, pp. 199 - 202 DOI: 10.1126/science.279.5348.199
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Reports
Engineering Broader Specificity into an Antibiotic-Producing Polyketide Synthase
Andrew F. A. Marsden,
Barrie Wilkinson,
Jesús Cortés,
Nicholas J. Dunster,
James Staunton,
Peter F. Leadlay
*
The wide-specificity loading module for the avermectin-producing
polyketide synthase was grafted onto the first multienzyme component
(DEBS1) of the erythromycin-producing polyketide synthase in place of
the normal loading module. Expression of this hybrid enzyme in the
erythromycin producer Saccharopolyspora erythraea produced
several novel antibiotic erythromycins derived from endogenous branched-chain acid starter units typical of natural avermectins. Because the avermectin polyketide synthase is known to accept more than
40 alternative carboxylic acids as starter units, this approach opens
the way to facile production of novel analogs of antibiotic macrolides.
A. F. A. Marsden, J. Cortés, N. J. Dunster,
P. F. Leadlay, Cambridge Centre for Molecular Recognition and
Department of Biochemistry, University of Cambridge, Tennis Court Road,
Cambridge, CB2 1QW, UK.
B. Wilkinson and J. Staunton, Cambridge Centre for Molecular
Recognition and University Chemical Laboratory, University of
Cambridge, Lensfield Road, Cambridge, CB2 1EW, UK.
*
To whom correspondence should be addressed. E-mail:
pfl10{at}mole.bio.cam.ac.uk
Read the Full Text
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- S. Murli, K. S. MacMillan, Z. Hu, G. W. Ashley, S. D. Dong, J. T. Kealey, C. D. Reeves, and J. Kennedy (2005)
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- An efficient method for creation and functional analysis of libraries of hybrid type I polyketide synthases.
- B. S. Kim, D. H. Sherman, and K. A. Reynolds (2004)
Protein Eng. Des. Sel.
17, 277-284
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- A specific role of the Saccharopolyspora erythraea thioesterase II gene in the function of modular polyketide synthases.
- Z. Hu, B. A. Pfeifer, E. Chao, S. Murli, J. Kealey, J. R. Carney, G. Ashley, C. Khosla, and C. R. Hutchinson (2003)
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- Microbial Relatives of the Seed Storage Proteins of Higher Plants: Conservation of Structure and Diversification of Function during Evolution of the Cupin Superfamily.
- J. M. Dunwell, S. Khuri, and P. J. Gane (2000)
Microbiol. Mol. Biol. Rev.
64, 153-179
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- New Lessons for Combinatorial Biosynthesis from Myxobacteria. THE MYXOTHIAZOL BIOSYNTHETIC GENE CLUSTER OF Stigmatella aurantiaca DW4/3-1.
- B. Silakowski, H. U. Schairer, H. Ehret, B. Kunze, S. Weinig, G. Nordsiek, P. Brandt, H. Blocker, G. Hofle, S. Beyer, et al. (1999)
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- Interactions among enzymes of the Arabidopsis flavonoid biosynthetic pathway.
- I. E. Burbulis and B. Winkel-Shirley (1999)
PNAS
96, 12929-12934
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- A multiplasmid approach to preparing large libraries of polyketides.
- Q. Xue, G. Ashley, C. R. Hutchinson, and D. V. Santi (1999)
PNAS
96, 11740-11745
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- A host-vector system for analysis and manipulation of rifamycin polyketide biosynthesis in Amycolatopsis mediterranei.
- Z. Hu, D. Hunziker, C. R. Hutchinson, and C. Khosla (1999)
Microbiology
145, 2335-2341
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- Pseudomonas syringae Phytotoxins: Mode of Action, Regulation, and Biosynthesis by Peptide and Polyketide Synthetases.
- C. L. Bender, F. Alarcon-Chaidez, and D. C. Gross (1999)
Microbiol. Mol. Biol. Rev.
63, 266-292
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- Microbial polyketide synthases: More and more prolific.
- C. R. Hutchinson (1999)
PNAS
96, 3336-3338
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- Engineering precision RNA molecular switches.
- G. A. Soukup and R. R. Breaker (1999)
PNAS
96, 3584-3589
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- Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products.
- R. McDaniel, A. Thamchaipenet, C. Gustafsson, H. Fu, M. Betlach, M. Betlach, and G. Ashley (1999)
PNAS
96, 1846-1851
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- Combinatorial biosynthesis: Lesson learned from nature.
- K. A. Reynolds (1998)
PNAS
95, 12744-12746
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- Harnessing the Biosynthetic Code: Combinations, Permutations, and Mutations.
- D. E. Cane, C. T. Walsh, and C. Khosla (1998)
Science
282, 63-68
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- beta -Lactam synthetase: A new biosynthetic enzyme.
- B. O. Bachmann, R. Li, and C. A. Townsend (1998)
PNAS
95, 9082-9086
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- Ethyl-substituted erythromycin derivatives produced by directed metabolic engineering.
- D. L. Stassi, S. J. Kakavas, K. A. Reynolds, G. Gunawardana, S. Swanson, D. Zeidner, M. Jackson, H. Liu, A. Buko, and L. Katz (1998)
PNAS
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