The Discovery of New Cyanobactins from Cyanothece PCC 7425 Defines a New Signature for Processing of Patellamides

被引:34
作者
Houssen, Wael E. [2 ,3 ]
Koehnke, Jesko [1 ]
Zollman, David [1 ]
Vendome, Jeremie [4 ,5 ]
Raab, Andrea [2 ]
Smith, Margaret C. M. [3 ]
Naismith, James H. [1 ]
Jaspars, Marcel [2 ]
机构
[1] Univ St Andrews, St Andrews KY16 9ST, Fife, Scotland
[2] Univ Aberdeen, Dept Chem, Marine Biodiscovery Ctr, Aberdeen AB24 3UE, Scotland
[3] Univ Aberdeen, Sch Med Sci, Inst Med Sci, Aberdeen AB25 2ZD, Scotland
[4] Columbia Univ, Dept Biochem & Mol Biophys, New York, NY 10032 USA
[5] Columbia Univ, Howard Hughes Med Inst, New York, NY 10032 USA
基金
英国生物技术与生命科学研究理事会;
关键词
biosynthetic engineering; cyanobactins; natural products; ribosomal peptides; subtilisin proteases; MARINE NATURAL-PRODUCTS; LISSOCLINUM-PATELLA; GENE-CLUSTER; PEPTIDE; SEQUENCE; MACROCYCLIZATION; BIOSYNTHESIS; REFINEMENT; EXPRESSION; SUBTILISIN;
D O I
10.1002/cbic.201200661
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Cyanobactins, including patellamides, are a group of cyanobacterial post-translationally modified ribosomal cyclic peptides. The final product should in theory be predictable from the sequence of the precursor peptide and the associated tailoring enzymes. Understanding the mechanism and recognition requirements of these enzymes will allow their rational engineering. We have identified three new cyanobactins from a Cyanothece PCC 7425 culture subjected to a heat shock. One of these compounds revealed a novel signature signal for ThcA, the subtilisin-like serine protease that is homologous to the patellamide protease PatA. The crystal structure of the latter and modelling studies allow rationalisation of the recognition determinants for both enzymes, consistent with the ribosomal biosynthetic origin of the new compounds.
引用
收藏
页码:2683 / 2689
页数:7
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