Engineered biosynthesis of gilvocarcin analogues with altered deoxyhexopyranose moieties.

Abstract

A combinatorial biosynthetic approach was used to interrogate the donor substrate flexibility of GilGT, the glycosyltransferase involved in C-glycosylation during gilvocarcin biosynthesis. Complementation of gilvocarcin mutant Streptomyces lividans TK24 (cosG9B3-U(-)), in which the biosynthesis of the natural sugar donor substrate was compromised, with various deoxysugar plasmids led to the generation of six gilvocarcin analogues with altered saccharide moieties. Characterization of the isolated gilvocarcin derivatives revealed five new compounds, including 4-β-C-D-olivosyl-gilvocarcin V (D-olivosyl GV), 4-β-C-D-olivosyl-gilvocarcin M (D-olivosyl GM), 4-β-C-D-olivosyl-gilvocarcin E (D-olivosyl GE), 4-α-C-L-rhamnosyl-gilvocarcin M (polycarcin M), 4-α-C-L-rhamnosyl-gilvocarcin E (polycarcin E), and the recently characterized 4-α-C-L-rhamnosyl-gilvocarcin V (polycarcin V). Preliminary anticancer assays showed that D-olivosyl-gilvocarcin and polycarcin V exhibit antitumor activities comparable to that of their parent drug congener, gilvocarcin V, against human lung cancer (H460), murine lung cancer (LL/2), and breast cancer (MCF-7) cell lines. Our findings demonstrate GilGT to be a moderately flexible C-glycosyltransferase able to transfer both D- and L-hexopyranose moieties to the unique angucyclinone-derived benzo[D]naphtho[1,2b]pyran-6-one backbone of the gilvocarcins.

• Authors: Micah D Shepherd, Tao Liu, Carmen Méndez, Jose A Salas, Jürgen Rohr
• Journal: Applied and environmental microbiology (Appl Environ Microbiol) Vol. 77 Issue 2 Pg. 435-41 (Jan 2011) ISSN: 1098-5336 [Electronic] United States
• PMID: 21075894 (Publication Type: Journal Article, Research Support, N.I.H., Extramural)

Chemical References

• Aminoglycosides
• Antineoplastic Agents
• Coumarins
• Deoxy Sugars
• 2,4-dideoxyhexopyranose
• coumarin

Topics

• Aminoglycosides (metabolism)
• Animals
• Antineoplastic Agents (metabolism)
• Biosynthetic Pathways (genetics)
• Cell Line, Tumor
• Cell Survival (drug effects)
• Coumarins (chemistry, metabolism)
• Deoxy Sugars (metabolism)
• Humans
• Mice
• Streptomyces lividans (enzymology, genetics, metabolism)