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Journal of Bacteriology, August 2004, p. 5187-5188, Vol. 186, No. 16
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.16.5187-5188.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.

Identification of a Key Step in the Biosynthetic Pathway of Bacteriochlorophyll c and Its Implications for Other Known and Unknown Green Sulfur Bacteria

Robert E. Blankenship*

Department of Chemistry and Biochemistry, Arizona State University, Tempe, Arizona 85287-1604


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INTRODUCTION
 
The enzyme responsible for the methylation at the C-20 methine position of the bacteriochlorophylls c and e found in green sulfur photosynthetic bacteria has been identified by genomics and knockout mutagenesis. The distribution of this enzyme in other green sulfur bacteria is surprising.


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ULTRAWEAK LIGHT COLLECTION BY GREEN PHOTOSYNTHETIC BACTERIAL ANTENNAS
 
The green photosynthetic bacteria are the world champions of doing photosynthesis at low light intensities (7). They accomplish this by using a unique antenna complex known as a chlorosome, which is packed with specialized photopigments, bacteriochlorophylls c, d, and e (1). These unusual chlorophylls are not found in any other organisms, and they self-assemble into large pigment oligomers with almost no involvement of protein. This biosynthetically "cheap" antenna complex has an enormous absorption cross-section and permits certain of these organisms to live at the lowest light intensities known to support photosynthesis, up to a million times lower light than normal sunlight (8). At these low intensities, each bacteriochlorophyll absorbs a photon approximately once every 8 h! A key step in the biosynthesis of bacteriochlorophylls c and e (but not d) is the methylation at the C-20 position of the chlorin macrocycle (Fig. 1). The enzyme that carries out this methylation (BchU) has previously not been identified. However, in a recently published paper, Maresca et al. (4) identify the methyltransferase enzyme in Chlorobium tepidum by using a combination of comparative genomics and knockout mutagenesis.



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  		FIG. 1. Chemical structures of bacteriochlorophylls c, d, e, and f. The structural features that differentiate these four pigments are circled. The C-20 methine position (solid circle) is methyl in bacteriochlorophylls c and e and hydrogen in bacteriochlorophylls d and f. The C-7 position (dashed circle) is methyl in bacteriochlorophylls c and d and formyl in bacteriochlorophylls e and f. R1 can be ethyl, n-propyl, iso-butyl, or neo-pentyl; R2 is methyl or ethyl; and R3 is, in most cases, farnesyl.

The investigators did some clever detective work to identify the gene that codes for the C-20 methyltransferase. The complete Chlorobium tepidum genome sequence has been determined (3), but the genome contains many potential methyltransferase genes and initial guesses were not correct. The identification was made by comparative genomics with the filamentous anoxygenic phototrophic (FAP) bacteria, also often called the green nonsulfur bacteria. These organisms are the only other major group of bacteria that contain the chlorosome antenna complex, although overall they are not close relatives of the green sulfur bacteria, and a draft genome is available for one member of this group, Chloroflexus aurantiacus. Fortunately, genes that code for chlorosome components are clustered in the FAP bacteria, while they are not in the green sulfur bacteria, and this clustering suggested a methyltransferase gene as a good candidate for the C-20 methylase. A knockout mutation in Chlorobium tepidum had the expected phenotype of containing bacteriochlorophyll d, which lacks the C-20 methyl group, instead of bacteriochlorophyll c. This established the identity of the gene, which was named bchU (4).


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A SURPRISE FINDING AND SOME PREDICTIONS
 
Other groups of green photosynthetic bacteria contain functional chlorosomes that contain only bacteriochlorophyll d. Maresca et al. (4) examined some of these strains. A surprise in their findings is that at least one "wild-type" bacteriochlorophyll d-containing organism also contains a bchU gene, but with a frameshift mutation that leads to premature termination and an inactive enzyme. Certain bacteriochlorophyll d-containing strains have long been known to be prone to reversion to making bacteriochlorophyll c when grown for extended periods at low light intensities (2). In some of these strains, Maresca et al. (4) found that a second mutation restores the original reading frame and results in an active methyltransferase enzyme. Interesting questions remain about the observed distribution of these bacteriochlorophyll d-containing organisms in nature and how the C-20 methyl group affects the efficiency of light collection. In laboratory growth competition experiments, Maresca et al. (4) found that the bacteriochlorophyll d-containing Chlorobium tepidum bchU mutant cells did not grow as rapidly as the bacteriochlorophyll c-containing wild type under low light conditions but grew at the same rate at higher light intensity.

Can it be that all bacteriochlorophyll d-containing strains (which are often dominant isolates at somewhat higher positions in the water column and therefore higher light intensities) really contain a bchU gene that is inactivated by a frameshift and susceptible to reversion? This seems unlikely, but this question could be easily resolved by analysis of a series of bacteriochlorophyll d-containing strains. It may be that some of the common laboratory bacteriochlorophyll d-containing strains have arisen in the laboratory by selective pressure due to culturing at higher light intensities and that newly isolated bacteriochlorophyll d-containing strains will lack the gene entirely.

There is one additional pigment in the series of pigments that comprise the chlorobium chlorophylls, bacteriochlorophyll f (Fig. 1). This pigment has never been observed in nature, but it is the logical final member of this series of pigments, in that it contains hydrogen at C-20 and formyl at C-7. According to the progression of in vivo absorption maxima, in which bacteriochlorophyll c typically absorbs at 750 to 760 nm, bacteriochlorophyll d at 725 to 735 nm, and bacteriochlorophyll e at 710 to 720 nm, bacteriochlorophyll f should absorb at about 690 to 710 nm. It is a bit of a mystery why bacteriochlorophyll f-containing organisms have never been found, as both of the enzymes that make the two functional groups are clearly present in closely related species. The predicted 690- to 710-nm spectral window would appear to be a niche that is not well exploited, as it is just to the red of the chlorophyll a absorption band that is usually dominant. The only other known organisms that absorb in this spectral region are the chlorophyll d-containing cyanobacteria, which are not widely distributed (5).

It should be possible to produce an organism that contains bacteriochlorophyll f, simply by knocking out the C-20 methyltransferase enzyme in a bacteriochlorophyll e-containing strain. While none of the bacteriochlorophyll e-containing strains have genetic systems yet available, this should still be relatively straightforward.

A final puzzle yet to be solved is the identification of the enzyme that makes the formyl group at the C-7 position in bacteriochlorophyll e. This is the same position and functional group that is found in chlorophyll b. However, the enzymes are almost certainly not homologous, as the enzyme that makes chlorophyll b is a mixed-function oxidase that relies on O2 as a substrate (9) and the bacteriochlorophyll e-containing bacteria are strict anaerobes. This is almost certainly another in a growing group of cases of gene replacement, in which the same biosynthetic steps are carried out by entirely different enzymes in anaerobic and aerobic organisms, with only the aerobic enzymes using O2 as a substrate. Other examples include the coproporphyrinogen oxidase involved in heme and chlorophyll biosynthesis (HemN versus HemF), the oxidative cyclase that makes the isocyclic ring in chlorophylls (BchE versus AcsF), and ribonucleotide reductase (NrdG versus NrdB) (6). The anaerobic versions are probably the more ancient enzymes, dating to a time more than 2.2 billion years ago when the earth was largely anaerobic, and the more efficient aerobic versions that use the powerful oxidant O2 have replaced the older ones whenever possible.


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FOOTNOTES
 
* Mailing address: Department of Chemistry and Biochemistry, Arizona State University, Tempe, AZ 85287-1604. Phone: (480) 965-4430. Fax: (480) 965-2747. E-mail: Blankenship{at}asu.edu. Back

The views expressed in this Commentary do not necessarily reflect the views of the journal or of ASM.


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REFERENCES
 
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  1. Blankenship, R. E., and K. Matsuura. 2003. Antenna complexes from green photosynthetic bacteria, p. 195-217. In B. R. Green and W. W. Parson (ed.), Light harvesting antennas. Kluwer Academic Publishing, Dordrecht, The Netherlands.
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  2. Bobe, F. W., N. Pfennig, K. L. Swanson, and K. M. Smith. 1990. Red shift of absorption maxima in Chlorobiineae through enzymic methylation of their antenna bacteriochlorophylls. Biochemistry 29:4340-4348.[CrossRef][Medline]
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  3. Eisen, J. A., K. E. Nelson, I. T. Paulsen, J. F. Heidelberg, M. Wu, R. J. Dodson, R. Deboy, M. L. Gwinn, W. C. Nelson, D. H. Haft, E. K. Hickey, J. D. Peterson, A. S. Durkin, J. L. Kolonay, F. Yang, I. Holt, L. A. Umayam, T. Mason, M. Brenner, T. P. Shea, D. Parksey, W. C. Nierman, T. V. Feldblyum, C. L. Hansen, M. B. Craven, D. Radune, J. Vamathevan, H. Khouri, O. White, T. M. Gruber, K. A. Ketchum, J. C. Venter, H. Tettelin, D. A. Bryant, and C. M. Fraser. 2002. The complete genome sequence of Chlorobium tepidum TLS, a photosynthetic, anaerobic, green-sulfur bacterium. Proc. Natl. Acad. Sci. USA 99:9509-9514.[Abstract/Free Full Text]
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  4. Maresca, J. A., A. G. M. Chew, M. R. Ponsati, N.-U. Frigaard, J. G. Ormerod, and D. A. Bryant. 2004. The bchU gene of Chlorobium tepidum encodes the C-20 methyltransferase in bacteriochlorophyll c biosynthesis. J. Bacteriol. 186:2558-2566.[Abstract/Free Full Text]
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  5. Miyashita, H., H. Ikemoto, N. Kurano, K. Adachi, M. Chihara, and S. Miyachi. 1996. Chlorophyll d as a major pigment. Nature 383:402.[CrossRef]
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  6. Ouchane, S., A. S. Steunou, M. Picaud, and C. Astier. 2004. Aerobic and anaerobic Mg-protoporphyrin monomethyl ester cyclases in purple bacteria—a strategy adopted to bypass the repressive oxygen control system. J. Biol. Chem. 279:6385-6394.[Abstract/Free Full Text]
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  7. Overmann, J. 2001. Green sulfur bacteria, p. 601-605. In D. R. Boone and R. W. Castenholz (ed.), Bergey's manual of systematic bacteriology, 2nd ed. Springer, New York, N.Y.
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  8. Overmann, J., H. Cypionka, and N. Pfennig. 1992. An extremely low light adapted phototrophic sulfur bacterium from the Black Sea. Limnol. Oceanogr. 37:150-155.
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  9. Tanaka, A., H. Ito, R. Tanaka, N. K. Tanaka, K. Yoshida, and K. Okada. 1998. Chlorophyll a oxygenase (CAO) is involved in chlorophyll b formation from chlorophyll a. Proc. Natl. Acad. Sci. USA 95:12719-12723.[Abstract/Free Full Text]

Journal of Bacteriology, August 2004, p. 5187-5188, Vol. 186, No. 16
0021-9193/04/$08.00+0     DOI: 10.1128/JB.186.16.5187-5188.2004
Copyright © 2004, American Society for Microbiology. All Rights Reserved.




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