4.4 Article

Aromatic C-Methyltransferases with Antipodal Stereoselectivity for Structurally Diverse Phenolic Amino Acids Catalyze the Methylation Step in the Biosynthesis of the Actinomycin Chromophore

Journal

BIOCHEMISTRY
Volume 49, Issue 45, Pages 9698-9705

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/bi101422r

Keywords

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Funding

  1. Deutsche Forschungsgemeinschaft [Ke 452/8-4, Ke 452/11-4, SPP1152]
  2. Unicat Center of Excellence of the Deutsche Forschungsgemeinschaft at the Technische Universitat Berlin

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The actinomycin biosynthetic gene cluster of Streptomyces chrysomallus harbors two paralogous genes, acmI and acmL, encoding methyltransferases. To unveil their suspected role in the formation of 3-hydroxy-4-methyl-anthranilic acid (4-MHA), the building block of the actinomycin chromophore, each gene was expressed in Escherichia coli. Testing the resulting similar to 40 kDa His(6)-tagged proteins with compounds of biogenetic relevance as substrates and S-adenosyl-L-methionine revealed that each exclusively methylated 3-hydroxykynurenine (3-HK) with formation of 3-hydroxy-4-methylkynurenine (4-MHK) identified by its in vitro conversion to 4-MHA with hydroxykynureninase. AcmI and AcmL methylate also hydroxyphenylamino propanoic acids such as p-tyrosine, m-tyrosine, or 3,4-dihydroxy-L-phenylalanine (DOPA) but at a lower rate than 3-HK. The presence of the alpha-amino group was necessary for substrate recognition. Phenolic acids with shorter chains such as 4-hydoxyphenyl-L-glycine (HPG), 3-hydroxybenzoic acid (3-HB), or 3-hydroxyanthranilic acid (3-HA) gave no product. Both enzymes were stereospecific for the optical configuration at alpha-C with unprecedented antipodal selectivity for the D-enantiomer of 3-HK and the L-enantiomer of p-tyrosine or m-tyrosine. AcmI and AcmL show sequence similarity to various C- and O-methyltransferases from bacteria. Phylogenetic analysis places them into the clade of C-methyltransferases comprising among others orthologues involved in 4-MHA formation of other biosynthesis systems and methyltransferases putatively involved in the C-methylation of tyrosine. Remarkably, computational remodelling of AcmI and AcmL structures revealed significant similarity with the 3-D structures of type 1 O-methyltransferases from plants such as caffeic acid O-methyltransferase (COMT) and other phenylpro-panoid methyltransferases. The relevance of 3-HK or 3-HA methylation in the actinomycin biosynthesis pathways of different actinomycetes is discussed.

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