SBIR-STTR Award

Modification of daptomycin by combinatorial biosynthesis
Award last edited on: 11/22/05

Sponsored Program
SBIR
Awarding Agency
NIH : NIGMS
Total Award Amount
$1,158,205
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Paul Brian

Company Information

Cubist Pharmaceuticals Inc

65 Hayden Avenue
Lexington, MA 02421
   (781) 860-8660
   N/A
   www.cubist.com
Location: Single
Congr. District: 05
County: Middlesex

Phase I

Contract Number: 1R43GM068173-01
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2003
Phase I Amount
$258,205
The antibiotic daptomycin is produced by the Gram-positive bacterium Streptomyces roseosporus and is the first in a new class of investigational drugs called lipopeptides that is being developed by Cubist for the treatment of serious and life-threatening infections caused by Gram-positive pathogens. The goal of this phase I application is to develop a system that will allow the rapid manipulation of the daptomycin biosynthetic gene cluster. These tools would then be used in phase II of the application to elucidate the structure-activity realtionships (SAR) of daptomycin and use this information to create derivatives of daptomycin with increased potency against vancomycin resistant pathogens.

Thesaurus Terms:
Streptomyces, antibiotic, chemical structure function, combinatorial chemistry, cyclic peptide, drug design /synthesis /production, molecular cloning biotherapeutic agent, stereochemistry biotechnology, plasmid

Phase II

Contract Number: 2R44GM068173-02
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2004
(last award dollars: 2005)
Phase II Amount
$900,000

The antibiotic daptomycin is produced by the Gram-positive bacterium Streptomyces roseosporus and is the first in a new class of investigational drugs called lipopeptides that is being developed by Cubist for the treatment of serious and life-threatening infections caused by Gram-positive pathogens. The goal of this phase I application is to develop a system that will allow the rapid manipulation of the daptomycin biosynthetic gene cluster. These tools would then be used in phase II of the application to elucidate the structure activity realtionships (SAR) of daptomycin and use this information to create derivatives of daptomycin with increased potency against vancomycin resistant pathogens.

Thesaurus Terms:
antibiotic, chemical structure function, combinatorial chemistry, cyclic peptide, drug design /synthesis /production microorganism metabolism Escherichia coli, Streptomyces, artificial chromosome, laboratory mouse, microorganism mass culture, plasmid, transfection