Document Detail


Engineered biosynthesis of novel polyketides: regiospecific methylation of an unnatural substrate by the tcmO O-methyltransferase.
MedLine Citation:
PMID:  8639600     Owner:  NLM     Status:  MEDLINE    
Abstract/OtherAbstract:
TcmO is an O-methyltransferase that methylates the C-8 hydroxyl to Tcm B3, a four-ring aromatic intermediate in the tetracenomycin biosynthetic pathway of Streptomyces glaucescens. The gene encoding this enzyme was expressed in Streptomyces coelicolor CH999 together with the actinorhodin polyketide synthase (PKS) gene cluster, which is responsible for the biosynthesis of 3,8-dihydroxy-methylanthraquinone carboxylic acid (DMAC) and its decarboxylated analog, aloesaponarin. The resulting recombinant strain produced approximately equal quantities of aloesaponarin and a new product but no DMAC. Spectroscopic analysis revealed that the novel polyketide was the 3-O-methylated analog of DMAC. An in vitro radioisotopic assay was developed for tcmO. The enzyme requires S-adenosylmethionine as a co-substrate. It has a Km of 3 microM and a kcat of 2.7 min-1 for DMAC. A series of monocyclic, bicyclic, and tricyclic aromatic compounds were also tested as candidate substrates in vitro. Remarkably, none was modified by tcmO within detectable limits of the assay. Together, these results highlight the interesting molecular recognition features of this enzyme. On one hand, there appears to be some flexibility in the number and structures of unreactive rings, since both Tcm and B3 and DMAC are good substrates. However, 6-methylsalicylic acid, a monocyclic analog of the reactive ring, is not recognized by the enzyme. Likewise, neither aloesaponarin (which only differs from DMAC in the reactive ring) nor carminic acid (which only differs in the distal nonreactive ring) is modified. Thus, the binding energy for the tcmO-catalyzed methyl transfer appears to involve significant contributions from both the aromaticity and the functionality of polycyclic substrates.
Authors:
H Fu; M A Alvarez; C Khosla; J E Bailey
Publication Detail:
Type:  Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, Non-P.H.S.    
Journal Detail:
Title:  Biochemistry     Volume:  35     ISSN:  0006-2960     ISO Abbreviation:  Biochemistry     Publication Date:  1996 May 
Date Detail:
Created Date:  1996-07-17     Completed Date:  1996-07-17     Revised Date:  2006-11-15    
Medline Journal Info:
Nlm Unique ID:  0370623     Medline TA:  Biochemistry     Country:  UNITED STATES    
Other Details:
Languages:  eng     Pagination:  6527-32     Citation Subset:  IM    
Affiliation:
Department of Chemical Engineering, Stanford University, California 94305-5025, USA.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:
Anthraquinones / chemistry,  metabolism*
Bacterial Proteins / genetics,  metabolism*
Cell-Free System
Cloning, Molecular
Genes, Bacterial
Kinetics
Methylation
Methyltransferases / genetics,  metabolism*
Multienzyme Complexes / biosynthesis,  genetics
Multigene Family
Naphthacenes / metabolism*
Recombinant Proteins / biosynthesis
Streptomyces / enzymology*,  genetics
Substrate Specificity
Chemical
Reg. No./Substance:
0/3,8-dihydroxy-1-methylanthraquinone-2-carboxylic acid; 0/Anthraquinones; 0/Bacterial Proteins; 0/Multienzyme Complexes; 0/Naphthacenes; 0/Recombinant Proteins; 146864-75-7/5838 DNI; EC 2.1.1.-/Methyltransferases; EC 2.1.1.-/TcmO protein, Streptomyces glaucescens

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Design challenges for hemoproteins: the solution structure of apocytochrome b5.
Next Document:  NMR studies of the effects of the 5'-phosphate group on conformational properties of 5-methylaminome...