Notice Number (NOT-OD-09-058) NIH Announces the Availability of Recovery Act Funds for Competitive Revision Applications Natural products are still the majority of therapeutic agents. However, they suffer from a difficulty in the creation of derivatives, and they can also be hard to supply. Derivatives are extremely important in the optimization of properties, such as toxicity or solubility that are critical to development of therapeutics. Recently, it has become increasingly popular to create libraries of derivatives using genetic engineering of natural product biosynthetic genes. Even in the best libraries, the numbers of derivatives are in the hundreds or low thousands. Recently, we discovered an evolutionary pathway that could potentially be harvested to generate tens of billions of derivatives. The compounds can be """"""""evolved"""""""" by directly challenging producing E. coli with different new environments. We hope to develop a system in which new activities can be pharmacologically optimized in a matter of days to weeks, exploring a huge diversity of unnatural natural products. To fully harness this unusual evolutionary property for application to human health needs, in this revision we propose to: 1) Characterize the chemical output of the ~8 million-scale library. We will determine whether there are any limits on the chemical output of this natural products biosynthetic pathway. 2) Apply assays that explore protein-protein interactions, antibiotic activity, and diagnostic capability of this library. We will test the suitability of these """"""""evolving"""""""" systems for broad and otherwise difficult target areas of therapeutic interest. 3) Optimize library compound expression and diversification. We will explore renewable expression and improve stable yields in E. coli. 4) Provide further pathway tools to add other post-translational modifications to the compounds. The suitability of new enzymes to library development will be explored.

Public Health Relevance

We will harness recent scientific discoveries to therapeutic areas including antibiotics, protein interaction diseases, and diagnostics (such as for cancers and immune diseases). Compounds discovered will be rapidly optimized to advance drug leads for preclinical testing.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
3R01GM071425-04S1
Application #
7815436
Study Section
Special Emphasis Panel (ZRG1-BCMB-H (95))
Program Officer
Jones, Warren
Project Start
2009-09-30
Project End
2010-12-31
Budget Start
2009-09-30
Budget End
2010-12-31
Support Year
4
Fiscal Year
2009
Total Cost
$397,047
Indirect Cost
Name
University of Utah
Department
Pharmacology
Type
Schools of Pharmacy
DUNS #
009095365
City
Salt Lake City
State
UT
Country
United States
Zip Code
84112
Ruffner, Duane E; Schmidt, Eric W; Heemstra, John R (2015) Assessing the combinatorial potential of the RiPP cyanobactin tru pathway. ACS Synth Biol 4:482-92
McIntosh, John A; Lin, Zhenjian; Tianero, Ma Diarey B et al. (2013) Aestuaramides, a natural library of cyanobactin cyclic peptides resulting from isoprene-derived Claisen rearrangements. ACS Chem Biol 8:877-83
Schmidt, Eric W; Donia, Mohamed S; McIntosh, John A et al. (2012) Origin and variation of tunicate secondary metabolites. J Nat Prod 75:295-304
Tianero, Ma Diarey B; Donia, Mohamed S; Young, Travis S et al. (2012) Ribosomal route to small-molecule diversity. J Am Chem Soc 134:418-25
Agarwal, Vinayak; Pierce, Elizabeth; McIntosh, John et al. (2012) Structures of cyanobactin maturation enzymes define a family of transamidating proteases. Chem Biol 19:1411-22
Donia, Mohamed S; Fricke, W Florian; Partensky, Frederic et al. (2011) Complex microbiome underlying secondary and primary metabolism in the tunicate-Prochloron symbiosis. Proc Natl Acad Sci U S A 108:E1423-32
Donia, Mohamed S; Schmidt, Eric W (2011) Linking chemistry and genetics in the growing cyanobactin natural products family. Chem Biol 18:508-19
Donia, Mohamed S; Fricke, W Florian; Ravel, Jacques et al. (2011) Variation in tropical reef symbiont metagenomes defined by secondary metabolism. PLoS One 6:e17897
McIntosh, John A; Donia, Mohamed S; Nair, Satish K et al. (2011) Enzymatic basis of ribosomal peptide prenylation in cyanobacteria. J Am Chem Soc 133:13698-705
Donia, Mohamed S; Ruffner, Duane E; Cao, Sheng et al. (2011) Accessing the hidden majority of marine natural products through metagenomics. Chembiochem 12:1230-6

Showing the most recent 10 out of 23 publications