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J. Bacteriol. doi:10.1128/JB.00519-07
Copyright (c) 2007, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.

Bacteriochlorophyllide c C-8² and C-12¹ methyltransferases are essential for adaptation to low light in Chlorobaculum tepidum

Department of Biochemistry and Molecular Biology, The Pennsylvania State University, University Park, PA 16802; Copenhagen Biocenter, Department of Molecular Biology, University of Copenhagen, Copenhagen, Denmark

^* To whom correspondence should be addressed. Email: dab14{at}psu.edu.

	Abstract

Bacteriochlorophyll (BChl) c is the major photosynthetic pigment in the green sulfur bacterium Chlorobaculum tepidum, in which it forms protein-independant aggregates that function in light harvesting. BChls c, d and e are only found in chlorosome-producing bacteria and are unique among chlorophylls because of methylations that occur at the C-8² and C-12¹ carbons. Two genes required for these methylation reactions were identified and designated bchQ (CT1777) and bchR (CT1320). BchQ and BchR are members of the radical-SAM protein superfamily, each has sequence motifs to ligate a [4Fe-4S] cluster, and we propose that they catalyze the methyl-group transfers. bchQ, bchR, and bchQ bchR mutants of C. tepidum were constructed and characterized. The bchQ mutant produced BChl c that was not methylated at C-8², the bchR mutant produced BChl c that was not methylated at C-12¹, and the double mutant produced [8-ethyl, 12-methyl]-BChl c that lacked methylation at both the C-8² and C12¹ positions. Compared to the wild type, the Q_y absorption bands for BChl c in the mutant cells were narrower and blue-shifted to varying extents. All three mutants grew slower and had a lower cellular BChl c content than wild type, an effect that was especially pronounced at low light intensities. These observations show that the C-8² and C-12¹ methylations of BChl c play important roles in the adaptation of C. tepidum to low light intensity. The data additionally suggest that these methylations also directly or indirectly affect the regulation of the BChl c biosynthetic pathway.