Inactivation of gilGT, encoding a C-glycosyltransferase, and gilOIII, encoding a P450 enzyme, allows the details of the late biosynthetic pathway to gilvocarcin V to be delineated

Tao Liu, Madan Kumar Kharel, Carsten Fischer, Andrew McCormick, Jürgen Rohr

Research output: Contribution to journalArticlepeer-review

33 Scopus citations

Abstract

Resequencing of the gilGT gene, which encodes a putative glycosyltransferase (GT) that is 495 amino acids (aa) long, from the Streptomyces griseoflavus Gö3592 gilvocarcin V (GV) gene cluster, revealed that the previously reported gilGT indeed contains two genes. These are the larger gilGT, which encodes the C-glycosyltransferase GilGT (379 aa), and the smaller gilV gene, which encodes an enzyme of unknown function (116 aa). The gene gilV is located immediately upstream of gilGT in the GV gene cluster. In-frame deletion of gilGT created a mutant that accumulated defucogilvocarcin E (defuco-GE). The result proves the function of GilGT as a C- glycosyltransferase. Deletion of gilOIII, which is located immediately downstream of gilGT, led to a mutant that accumulated gilvocarcin E (GE). This confirms that the corresponding P450 enzyme, GilOIII, is involved in the vinyl-group formation of GV. Cross-feeding experiments in which GE, defuco-GE, and defucogilvocarcin V (defuco-GV) were fed to an early blocked mutant of the GV biosynthetic pathway, showed that neither GE nor any of the defuco- compounds was an intermediate of the pathway.

Original languageEnglish
Pages (from-to)1070-1077
Number of pages8
JournalChemBioChem
Volume7
Issue number7
DOIs
StatePublished - Jul 2006

Funding

FundersFunder number
National Childhood Cancer Registry – National Cancer InstituteR01CA102102
National Childhood Cancer Registry – National Cancer Institute

    Keywords

    • Antitumor agents
    • Biosynthesis
    • Cytochrome P450
    • Gilvocarcin
    • Glycosylation

    ASJC Scopus subject areas

    • Biochemistry
    • Molecular Medicine
    • Molecular Biology
    • Organic Chemistry

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