Jizanpeptins, Cyanobacterial Protease Inhibitors from a Symploca sp. Cyanobacterium Collected in the Red Sea
Author(s) -
David A. Gallegos,
Josep Saurí,
Ryan D. Cohen,
Xuemei Wan,
Patrick Videau,
Alec VallotaEastman,
Lamiaa A. Shaala,
Diaa T. A. Youssef,
R. Thomas Williamson,
Gary E. Martin,
Benjamin Philmus,
Aleksandra E. Sikora,
Jane E. Ishmael,
Kerry L. McPhail
Publication year - 2018
Publication title -
journal of natural products
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.976
H-Index - 139
eISSN - 1520-6025
pISSN - 0163-3864
DOI - 10.1021/acs.jnatprod.8b00117
Subject(s) - cyanobacteria , protease , biology , chemistry , stereochemistry , botany , bacteria , biochemistry , enzyme , paleontology
Jizanpeptins A-E (1-5) are micropeptin depsipeptides isolated from a Red Sea specimen of a Symploca sp. cyanobacterium. The planar structures of the jizanpeptins were established using NMR spectroscopy and mass spectrometry and contain 3-amino-6-hydroxy-2-piperidone (Ahp) as one of eight residues in a typical micropeptin motif, as well as a side chain terminal glyceric acid sulfate moiety. The absolute configurations of the jizanpeptins were assigned using a combination of Marfey's methodology and chiral-phase HPLC analysis of hydrolysis products compared to commercial and synthesized standards. Jizanpeptins A-E showed specific inhibition of the serine protease trypsin (IC 50 = 72 nM to 1 μM) compared to chymotrypsin (IC 50 = 1.4 to >10 μM) in vitro and were not overtly cytotoxic to HeLa cervical or NCI-H460 lung cancer cell lines at micromolar concentrations.
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