Characterization of the Gene Cluster Responsible for Cylindrospermopsin Biosynthesis
Author(s) -
Troco Kaan Mihali,
Ralf Kellmann,
Julia Muenchhoff,
Kevin D. Barrow,
Brett A. Neilan
Publication year - 2007
Publication title -
applied and environmental microbiology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.552
H-Index - 324
eISSN - 1070-6291
pISSN - 0099-2240
DOI - 10.1128/aem.01988-07
Subject(s) - cylindrospermopsin , gene cluster , biosynthesis , biology , biochemistry , hydroxylation , gene , polyketide , cyanobacteria , genetics , enzyme , bacteria
Toxic cyanobacterial blooms cause economic losses and pose significant public health threats on a global scale. Characterization of the gene cluster for the biosynthesis of the cyanobacterial toxin cylindrospermopsin (cyr ) inCylindrospermopsis raciborskii AWT205 is described, and the complete biosynthetic pathway is proposed. Thecyr gene cluster spans 43 kb and is comprised of 15 open reading frames containing genes required for the biosynthesis, regulation, and export of the toxin. Biosynthesis is initiated via an amidinotransfer onto glycine followed by five polyketide extensions and subsequent reductions, and rings are formed via Michael additions in a stepwise manner. The uracil ring is formed by a novel pyrimidine biosynthesis mechanism and tailoring reactions, including sulfation and hydroxylation that complete biosynthesis. These findings enable the design of toxic strain-specific probes and allow the future study of the regulation and biological role of cylindrospermopsin.
Accelerating Research
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom
Address
John Eccles HouseRobert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom