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DESCRIPTION (provided by applicant): Bacterial type I modular polyketide synthases (PKSs) are complex, multifunctional enzymes that synthesize structurally diverse and medicinally relevant natural products. Given their modular organization, the manipulation of type I PKSs holds tremendous promise for the generation of novel macrolide antibiotics that are not easily accessible by standard chemical synthetic approaches. To fully harness this potential, however, a thorough evaluation of a variety of PKS systems is needed. To this end, the experiments described within this proposal seek to interface chemical synthesis with rigorous kinetic analysis and structural biology in an effort to enhance our understanding of specificity and catalysis of the pikromycin PKS system. In addition to providing detailed information regarding the kinetics of individual PKS modules, this work will also begin to uncover substrate specificity differences between the pikromycin and erythromycin (DEBS) PKS systems. Furthermore, a detailed understanding of the specificity of the pikromycin thioesterase domain will be achieved via x-ray co-crystallization studies.
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An innovative metabolic engineering strategy for the discovery of novel macrolide antibiotics
  • 批准号:
    9136308
  • 项目类别:
  • 资助金额:
    $22.49万
  • 财政年份:
    2016
  • 负责人:
    Jeffrey David Kittendorf
  • 依托单位:
A genetic engineering strategy for the improved production of the anti-helminthic
  • 批准号:
    8393663
  • 项目类别:
  • 资助金额:
    $17.05万
  • 财政年份:
    2012
  • 负责人:
    Jeffrey David Kittendorf
  • 依托单位:
A novel biosynthetic strategy for the production of a key cryptophycin precursor
  • 批准号:
    7998692
  • 项目类别:
  • 资助金额:
    $11.5万
  • 财政年份:
    2010
  • 负责人:
    Jeffrey David Kittendorf
  • 依托单位:
Specificity of Modular Polyketide Synthases
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