- About this Journal ·
- Abstracting and Indexing ·
- Advance Access ·
- Aims and Scope ·
- Annual Issues ·
- Article Processing Charges ·
- Articles in Press ·
- Author Guidelines ·
- Bibliographic Information ·
- Citations to this Journal ·
- Contact Information ·
- Editorial Board ·
- Editorial Workflow ·
- Free eTOC Alerts ·
- Publication Ethics ·
- Reviewers Acknowledgment ·
- Submit a Manuscript ·
- Subscription Information ·
- Table of Contents
International Journal of Evolutionary Biology
Volume 2012 (2012), Article ID 324549, 5 pages
Dispensabilities of Carbonic Anhydrase in Proteobacteria
1Life Science Research Center, College of Bioresource Sciences, Nihon University, 1866 Kameino, Fujisawa 252-0880, Japan
2Agricultural Bioinformatics Research Unit, Graduate School of Agriculture and Life Sciences, The University of Tokyo, Bunkyo-ku, Tokyo 113-8657, Japan
Received 10 February 2012; Accepted 14 March 2012
Academic Editor: Hideaki Nojiri
Copyright © 2012 Kenji Ueda et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
Carbonic anhydrase (CA) (E.C. 188.8.131.52) is a ubiquitous enzyme catalysing interconversion between CO2 and bicarbonate. The irregular distribution of the phylogenetically distinct classes of CA in procaryotic genome suggests its complex evolutionary history in procaryotes. Genetic evidence regarding the dispensability of CA under high-CO2 air in some model organisms indicates that CA-deficient microorganisms can persist in the natural environment by choosing high-CO2 niches. In this study, we studied the distribution of CA in the genome of Proteobacteria. While a large majority of the genome-sequenced Proteobacteria retained a CA gene(s), intracellular bacterial genera such as Buchnera and Rickettsia contained CA-defective strains. Comparison between CA-retaining and CA- deficient genomes showed the absence of whole coding sequence in some strains and the presence of frameshifted coding sequence in other strains. The evidence suggests that CA is inactivated and lost in some proteobacteria during the course of evolution based on its dispensability.
Carbonic anhydrase (CA) (EC 184.108.40.206) is a ubiquitous enzyme catalysing interconversion between CO2 and bicarbonate () [1, 2]. CA is fundamental to various biological functions including photosynthesis, respiration, and CO2 transport. To date, the existence of 3 major classes (alpha, beta, and gamma) of this enzyme has been known. Interestingly, no significant structural similarities are observed among these classes. Based on this feature, CA is recognised as an excellent example of convergent evolution [1, 2]. Most of the mammalian and plant CA specifically belong to alpha and beta class, respectively. On the other hand, the distribution of CA in procaryotes is irregular; some retain multiple classes of CA or multiple enzymes from the same class, and others do not retain any class of CA. Hence, it is likely that the evolution of CA function in procaryotes has a complex historical background .
Recently, a significant insight into the role of procaryotic CA has been provided by genetic studies in some model organisms such as Ralstonia eutropha  Escherichia coli , and Saccharomyces cerevisiae . Knockout mutants for CA of these microorganisms are unable to grow under ambient air but normally grow under an atmosphere with high levels (1–5%) of CO2.
This phenomenon is explained by the necessity of bicarbonate in the reaction catalysed by several housekeeping enzymes such as phosphoenolpyruvate carboxylase, carbamoyl phosphate synthase, and acetyl-CoA carboxylase [4, 5]. CA-positive microorganisms can generate bicarbonate from environmental CO2 by the catalytic reaction of CA and supply it to these enzymes, but CA-negative ones cannot. Hence, the former can grow even under ambient air containing a low level of CO2 (0.035%), but the latter cannot initiate growth unless they are supplied with a sufficient concentration of bicarbonate. The latter organisms, however, can grow under a high-CO2 atmosphere since it generates a high concentration of bicarbonate to maintain natural equilibrium. This in turn indicates that CA is not essential for microbial growth under high-CO2 environments, such as in soil, seawater, intestine, and some other syntrophic and commensal situations. Our previous study showed that an E. coli CA mutant was able to grow even under ambient air when it was cocultured with Bacillus subtilis .
The above-mentioned knowledge makes us speculate that the study of CA distribution in microbial genome will provide an insight into the history of adaptation of microorganisms to environment. Recently, we described that Symbiobacterium thermophilum, a unique syntrophic bacterium that effectively grows in coculture with a cognate Geobacillus stearothermophilus , lost CA in the course of evolution . Our studies have shown that S. thermophilum grows on high CO2 supply from environment and that this could be the reason for the absence of CA from its genome . The phylogeny of CA distributed in Clostridia to which S. thermophilum belongs indicated that the common ancestor of this group of bacteria retained a CA gene and that S. thermophilum lost CA in the course of its adaptation to high CO2 environments .
To deepen our insight into the correlation between CA deficiency and adaptation to high CO2 environments, we studied the distribution of CA in the phylum Proteobacteria. Proteobacteria consists of five distinctive classes (alpha, beta, gamma, delta, and epsilon) and unclassified classes including the genus Magnetococcus (http://www.ncbi.nlm.nih.gov/genome/). To date (February 1, 2012), complete genome sequence information is available with regard to 649 strains of 249 genera (supplementary Table S1 in Supplementary Material available online at doi:http://dx.doi.org/10.1155/2012/324549). Our search for the presence of CA by using the pathway database available at GenomeNet (http://www.genome.jp/) and BLAST searches (protein-protein searches based on BLOSUM62 scoring matrix) using known protein sequences annotated to be CA (corresponding to the protein encoded by the intact CA coding sequences shown in Figure 1) as queries showed that 39 strains of 20 genera (Table 1) of the genome-sequenced Proteobacteria do not retain any gene encoding CA.
Among the CA-deficient 20 genera, 4 genera (Buchnera, Blochmannia, Rickettsia, and Orientia) contained multiple CA-deficient strains (Table 1). These were obligate intracellular bacteria. It is known that endosymbionts lack genes involved in primary metabolism. For example, Buchnera sp. lacks amino acid biosynthesis genes, which are compensated for by the activity of the host organism . Such genetic defects in symbionts genome have probably occurred after establishing a tight, symbiotic relationship with the host organism. Presumably, the intracellular environments contain a high level of CO2; hence the catalytic function of CA is not necessary for the bacteria habituating in such environments. On the other hand, some intracellular bacteria such as Wolbachia retain a putative CA gene (supplementary Table S1). This suggests that intracellular environment does not always compensate for CA deficiency.
13 out of the 20 CA-deficient genera contained only a single genome-sequenced strain (supplementary Table S1). They include intracellular Candidatus bacteria and lithoautotrophic and sulfate-reducing bacteria. It is not yet known whether the defect is a common feature of the genus or not, but it is possible that the CA deficiency is widespread among those intracellular bacteria as in the abovementioned genera.
Contrasting to the genuswide deficiency, the other 3 genera (Actinobacillus, Acidithiobacillus, and Bartonella) harboured strain-specific defect of CA (supplementary Table S1). In Acidithiobacillus, all strains except for Acidithiobacillus caldus retained the CA gene in the conserved gene cluster (the corresponding region of Acidithiobacillus ferrooxidans ATCC 23270 is shown in Figure 1(a)). Contrasting to this, A. caldus partially retained the conserved genes. While the genes upstream of CA were conserved, those downstream of CA including CA gene were not (Figure 1(a)). This makes us think of the possibility that the CA deficiency in A. caldus is due not to simple deletion but to a genetic rearrangement that has occurred in a relatively large scale.
Lack of CA gene in a conserved gene cluster was also observed with respect to the two species of Helicobacter, Helicobacter felis and Helicobacter bizzozeronii. All the genome-sequenced Helicobacter strains except for the two species contained the conserved gene cluster consisting of 6 coding sequences including CA gene (the corresponding region of Helicobacter pylori 26695 is shown in Figure 1(a)). Contrasting to this, the genome of the two Helicobacter spp. retained the conserved cluster lacking the coding region for CA (the corresponding region of H. felis is shown in Figure 1(a)). H. felis and H. bizzozeronii retained a CA gene in a different locus (corresponding to HFELIS_06160 and HBZC1_14670, resp.).
The other case of strain-specific CA deficiency was based on mutations in the coding sequence. Frameshift mutations inactivating CA gene were identified with respect to the four strains, Actinobacillus pleuropneumoniae JL03, Rickettsia heilongjiangensis, Rickettsia japonica, and Bartonella quintana (Figure 1(b)). These organisms retained a frame-shifted coding sequence exactly at the position corresponding to the locus where the intact CA ortholog is located in related strains (Figure 1(b)). The coding region of A. pleuropneumoniae JL03 and R. japonica contained a single-base deletion in the middle part (supplementary Figures S1 and S2). The coding region of R. heilongjiangensis lacked 95 bp corresponding to the N-terminal part of CA (supplementary Figure S2). B. quintana contained multiple mutations including two single-base deletions, one 8-base insertion, two single-base insertions, and one non-sense (ochre) mutation (supplementary Figure S3).
It is most likely that the abovementioned mutations inactivating the CA gene have been introduced into the ancestral intact coding sequence during the course of evolution. The diverged mode of mutation may reflect the process of how dispensable genes are lost from the bacterial genome. The existence of the strains carrying the inactivated coding sequence strongly suggests that the CA gene is not necessary for their persistency. It is not yet known how these mutant strains compensate for their CA deficiency, but we may reasonably speculate that it is correlated with the environmental CO2 content.
The CA-deficient genera described in this paper are usually handled under a microaerobic or anaerobic atmosphere containing 1–5% CO2 . Hence, the conventional isolation method for these organisms has made possible isolation of strains requiring high CO2. On the other hand, the standard isolation procedure for aerobic proteobacteria using ambient air prevents isolation of CO2-requiring strains. This makes us think of the possibility that the very high proportion of CA-positive strains (610 out of 649 strains) (supplementary Table S1) is due to the limitation of isolation condition and is not appropriately reflecting the true distribution of CA in Proteobacteria.
The evolution of microbial genome reflects the history of environmental change. We expect that comprehensive analyses regarding the distribution of specific adaptive functions in microbial genome will provide deep insights into the constitution of the ecosystem.
This study was supported by the High-Tech Research Center Project of the Ministry of Education, Culture, Sports, Science and Technology, Japan.
- L. S. Smith and J. G. Ferry, “Prokaryotic carbonic anhydrases,” FEMS Microbiology Reviews, vol. 24, no. 4, pp. 335–366, 2000.
- B. C. Tripp, K. Smith, and J. G. Ferry, “Carbonic anhydrase: new insights for an ancient enzyme,” The Journal of Biological Chemistry, vol. 276, no. 52, pp. 48615–48618, 2001.
- B. Kusian, D. Sultemeyer, and B. Bowien, “Carbonic anhydrase is essential for growth of Ralstonia eutropha at ambient CO2 concentrations,” Journal of Bacteriology, vol. 184, no. 18, pp. 5018–5026, 2002.
- C. Merlin, M. Masters, S. McAteer, and A. Coulson, “Why is carbonic anhydrase essential to Escherichia coli?” Journal of Bacteriology, vol. 185, no. 21, pp. 6415–6424, 2003.
- J. Aguilera, J. P. van Dijken, J. H. de Winde, and J. T. Pronk, “Carbonic anhydrase (Nce103p): an essential biosynthetic enzyme for growth of Saccharomyces cerevisiae at atmospheric carbon dioxide pressure,” Biochemical Journal, vol. 391, no. 2, pp. 311–316, 2005.
- T. O. Watsuji, T. Kato, K. Ueda, and T. Beppu, “CO2 supply induces the growth of Symbiobacterium thermophilum, a syntrophic bacterium,” Bioscience, Biotechnology, and Biochemistry, vol. 70, no. 3, pp. 753–756, 2006.
- K. Ueda and T. Beppu, “Lessons from studies of Symbiobacterium thermophilum, a unique syntrophic bacterium,” Bioscience, Biotechnology and Biochemistry, vol. 71, no. 5, pp. 1115–1121, 2007.
- H. Nishida, T. Beppu, and K. Ueda, “Symbiobacterium lost carbonic anhydrase in the course of evolution,” Journal of Molecular Evolution, vol. 68, no. 1, pp. 90–96, 2009.
- S. Shigenobu, H. Watanabe, M. Hattori, Y. Sakaki, and H. Ishikawa, “Genome sequence of the endocellular bacterial symbiont of aphids Buchnera sp. APS,” Nature, vol. 407, no. 6800, pp. 81–86, 2000.
- “The proteobacteria,” in Bergey's Manual of Systematic Bacteriology, D. J. Brenner, N. R. Krieg, J. T. Staley, and G. M. Garrity, Eds., vol. 2, Springer, New York, NY, USA, 2nd edition, 2005.