Abstract
Carbon dioxide fixation is carried out primarily through the Calvin-Benson-Bassham reductive pentose phosphate cycle, in which ribulose-1, 5-bisphosphate carboxylase/oxygenase (RubisCO) is the key enzyme. The primary structure of the large subunit of form I RubisCO is well conserved; however, four distinct types, A, B, C, and D, may be distinguished, with types A and B and types C and D more closely related to one another. To better understand the environmental regulation of RubisCO in Lake Erie phytoplanktonic microorganisms, we have isolated total RNA and DNA from four Lake Erie sampling sites. Probes prepared from RubisCO large-subunit genes (rbcL) of the freshwater cyanobacterium Synechococcus sp. strain PCC6301 (representative of type IB) and the diatom Cylindrotheca sp. strain N1 (representative of type ID) were hybridized to the isolated RNA and DNA. To quantitate rbcL gene expression for each sample, the amount of gene expression per gene dose (i.e., the amount of mRNA divided by the amount of target DNA) was determined. With a limited number of sampling sites, it appeared that type ID (diatom) rbcL gene expression per gene dose decreased as the sampling sites shifted toward open water. By contrast, a similar trend was not observed for cyanobacterial (type IB) rbcL gene expression per gene dose. Complementary DNA specific for rbcL was synthesized from Lake Erie RNA samples and used as a template for PCR amplification of portions of various rbcL genes. Thus far, a total of 21 clones of rbcL genes derived from mRNA have been obtained and completely sequenced from the Ballast Island site. For surface water samples, deduced amino acid sequences of five of six clones appeared to be representative of green algae. In contrast, six of nine sequenced rbcL clones from 10-m-deep samples were of chromophytic and rhodophytic lineages. At 5 m deep, the active CO2-fixing planktonic organisms represented a diverse group, including organisms related to Chlorella ellipsoidea, Cylindrotheca sp. strain N1, and Olisthodiscus luteus. Although many more samplings at diverse sites must be accomplished, the discovery of distinctly different sequences of rbcL mRNA at different water depths suggests that there is a stratification of active CO2-fixing organisms in western Lake Erie.
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Selected References
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- Becker-André M., Hahlbrock K. Absolute mRNA quantification using the polymerase chain reaction (PCR). A novel approach by a PCR aided transcript titration assay (PATTY). Nucleic Acids Res. 1989 Nov 25;17(22):9437–9446. doi: 10.1093/nar/17.22.9437. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Boczar B. A., Delaney T. P., Cattolico R. A. Gene for the ribulose-1,5-bisphosphate carboxylase small subunit protein of the marine chromophyte Olisthodiscus luteus is similar to that of a chemoautotrophic bacterium. Proc Natl Acad Sci U S A. 1989 Jul;86(13):4996–4999. doi: 10.1073/pnas.86.13.4996. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Chen J., Macfarlane S. A., Wilson T. M. An analysis of spontaneous deletion sites in soil-borne wheat mosaic virus RNA2. Virology. 1995 May 10;209(1):213–217. doi: 10.1006/viro.1995.1245. [DOI] [PubMed] [Google Scholar]
- Curtis S. E., Haselkorn R. Isolation and sequence of the gene for the large subunit of ribulose-1,5-bisphosphate carboxylase from the cyanobacterium Anabaena 7120. Proc Natl Acad Sci U S A. 1983 Apr;80(7):1835–1839. doi: 10.1073/pnas.80.7.1835. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dron M., Rahire M., Rochaix J. D. Sequence of the chloroplast DNA region of Chlamydomonas reinhardii containing the gene of the large subunit of ribulose bisphosphate carboxylase and parts of its flanking genes. J Mol Biol. 1982 Dec 25;162(4):775–793. doi: 10.1016/0022-2836(82)90547-2. [DOI] [PubMed] [Google Scholar]
- Freshwater D. W., Fredericq S., Butler B. S., Hommersand M. H., Chase M. W. A gene phylogeny of the red algae (Rhodophyta) based on plastid rbcL. Proc Natl Acad Sci U S A. 1994 Jul 19;91(15):7281–7285. doi: 10.1073/pnas.91.15.7281. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gibson J. L., Falcone D. L., Tabita F. R. Nucleotide sequence, transcriptional analysis, and expression of genes encoded within the form I CO2 fixation operon of Rhodobacter sphaeroides. J Biol Chem. 1991 Aug 5;266(22):14646–14653. [PubMed] [Google Scholar]
- Hartman F. C., Lee E. H. Examination of the function of active site lysine 329 of ribulose-bisphosphate carboxylase/oxygenase as revealed by the proton exchange reaction. J Biol Chem. 1989 Jul 15;264(20):11784–11789. [PubMed] [Google Scholar]
- Hwang S. R., Tabita F. R. Cloning and expression of the chloroplast-encoded rbcL and rbcS genes from the marine diatom Cylindrotheca sp. strain N1. Plant Mol Biol. 1989 Jul;13(1):69–79. doi: 10.1007/BF00027336. [DOI] [PubMed] [Google Scholar]
- Hwang S. R., Tabita F. R. Cotranscription, deduced primary structure, and expression of the chloroplast-encoded rbcL and rbcS genes of the marine diatom Cylindrotheca sp. strain N1. J Biol Chem. 1991 Apr 5;266(10):6271–6279. [PubMed] [Google Scholar]
- Igarashi Y., McFadden B. A., el-Gul T. Active site histidine in spinach ribulosebisphosphate carboxylase/oxygenase modified by diethyl pyrocarbonate. Biochemistry. 1985 Jul 16;24(15):3957–3962. doi: 10.1021/bi00336a024. [DOI] [PubMed] [Google Scholar]
- Jacobs J. D., Ludwig J. R., Hildebrand M., Kukel A., Feng T. Y., Ord R. W., Volcani B. E. Characterization of two circular plasmids from the marine diatom Cylindrotheca fusiformis: plasmids hybridize to chloroplast and nuclear DNA. Mol Gen Genet. 1992 May;233(1-2):302–310. doi: 10.1007/BF00587592. [DOI] [PubMed] [Google Scholar]
- Kariwa H., Kamimura M., Arikawa J., Yoshimatsu K., Takashima I., Hashimoto N. Characterization of the mode of Hantaan virus infection in adult mice using a nested reverse transcriptase polymerase chain reaction: transient virus replication in adult mice. Microbiol Immunol. 1995;39(1):35–41. doi: 10.1111/j.1348-0421.1995.tb02165.x. [DOI] [PubMed] [Google Scholar]
- Kostrzewa M., Valentin K., Maid U., Radetzky R., Zetsche K. Structure of the rubisco operon from the multicellular red alga Antithamnion spec. Curr Genet. 1990 Dec;18(5):465–469. doi: 10.1007/BF00309918. [DOI] [PubMed] [Google Scholar]
- Kusano T., Takeshima T., Inoue C., Sugawara K. Evidence for two sets of structural genes coding for ribulose bisphosphate carboxylase in Thiobacillus ferrooxidans. J Bacteriol. 1991 Nov;173(22):7313–7323. doi: 10.1128/jb.173.22.7313-7323.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lamar R. T., Schoenike B., Vanden Wymelenberg A., Stewart P., Dietrich D. M., Cullen D. Quantitation of fungal mRNAs in complex substrates by reverse transcription PCR and its application to Phanerochaete chrysosporium-colonized soil. Appl Environ Microbiol. 1995 Jun;61(6):2122–2126. doi: 10.1128/aem.61.6.2122-2126.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Le Guyader F., Dubois E., Menard D., Pommepuy M. Detection of hepatitis A virus, rotavirus, and enterovirus in naturally contaminated shellfish and sediment by reverse transcription-seminested PCR. Appl Environ Microbiol. 1994 Oct;60(10):3665–3671. doi: 10.1128/aem.60.10.3665-3671.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Lorimer G. H. Ribulosebisphosphate carboxylase: amino acid sequence of a peptide bearing the activator carbon dioxide. Biochemistry. 1981 Mar 3;20(5):1236–1240. doi: 10.1021/bi00508a028. [DOI] [PubMed] [Google Scholar]
- Meijer W. G., Arnberg A. C., Enequist H. G., Terpstra P., Lidstrom M. E., Dijkhuizen L. Identification and organization of carbon dioxide fixation genes in Xanthobacter flavus H4-14. Mol Gen Genet. 1991 Feb;225(2):320–330. doi: 10.1007/BF00269865. [DOI] [PubMed] [Google Scholar]
- Monceyron C., Grinde B. Detection of hepatitis A virus in clinical and environmental samples by immunomagnetic separation and PCR. J Virol Methods. 1994 Feb;46(2):157–166. doi: 10.1016/0166-0934(94)90100-7. [DOI] [PubMed] [Google Scholar]
- Ogihara Y., Terachi T., Sasakuma T. Molecular analysis of the hot spot region related to length mutations in wheat chloroplast DNAs. I. Nucleotide divergence of genes and intergenic spacer regions located in the hot spot region. Genetics. 1991 Nov;129(3):873–884. doi: 10.1093/genetics/129.3.873. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pichard S. L., Paul J. H. Gene expression per gene dose, a specific measure of gene expression in aquatic microorganisms. Appl Environ Microbiol. 1993 Feb;59(2):451–457. doi: 10.1128/aem.59.2.451-457.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pichard Scott L., Paul John H. Detection of Gene Expression in Genetically Engineered Microorganisms and Natural Phytoplankton Populations in the Marine Environment by mRNA Analysis. Appl Environ Microbiol. 1991 Jun;57(6):1721–1727. doi: 10.1128/aem.57.6.1721-1727.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Pridmore R. D. New and versatile cloning vectors with kanamycin-resistance marker. Gene. 1987;56(2-3):309–312. doi: 10.1016/0378-1119(87)90149-1. [DOI] [PubMed] [Google Scholar]
- Reichelt B. Y., Delaney S. F. The nucleotide sequence for the large subunit of ribulose 1,5-bisphosphate carboxylase from a unicellular cyanobacterium, Synechococcus PCC6301. DNA. 1983;2(2):121–129. doi: 10.1089/dna.1983.2.121. [DOI] [PubMed] [Google Scholar]
- Song K., Osborn T. C. A method for examining expression of homologous genes in plant polyploids. Plant Mol Biol. 1994 Nov;26(4):1065–1071. doi: 10.1007/BF00040689. [DOI] [PubMed] [Google Scholar]
- Tabita F. R. Molecular and cellular regulation of autotrophic carbon dioxide fixation in microorganisms. Microbiol Rev. 1988 Jun;52(2):155–189. doi: 10.1128/mr.52.2.155-189.1988. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsai Y. L., Sobsey M. D., Sangermano L. R., Palmer C. J. Simple method of concentrating enteroviruses and hepatitis A virus from sewage and ocean water for rapid detection by reverse transcriptase-polymerase chain reaction. Appl Environ Microbiol. 1993 Oct;59(10):3488–3491. doi: 10.1128/aem.59.10.3488-3491.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsai Y. L., Tran B., Palmer C. J. Analysis of viral RNA persistence in seawater by reverse transcriptase-PCR. Appl Environ Microbiol. 1995 Jan;61(1):363–366. doi: 10.1128/aem.61.1.363-366.1995. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Tsai Y. L., Tran B., Sangermano L. R., Palmer C. J. Detection of poliovirus, hepatitis A virus, and rotavirus from sewage and ocean water by triplex reverse transcriptase PCR. Appl Environ Microbiol. 1994 Jul;60(7):2400–2407. doi: 10.1128/aem.60.7.2400-2407.1994. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Valentin K., Zetsche K. Nucleotide sequence of the gene for the large subunit of Rubisco from Cyanophora paradoxa--phylogenetic implications. Curr Genet. 1990 Oct;18(3):199–202. doi: 10.1007/BF00318380. [DOI] [PubMed] [Google Scholar]
- Zurawski G., Perrot B., Bottomley W., Whitfeld P. R. The structure of the gene for the large subunit of ribulose 1,5-bisphosphate carboxylase from spinach chloroplast DNA. Nucleic Acids Res. 1981 Jul 24;9(14):3251–3270. doi: 10.1093/nar/9.14.3251. [DOI] [PMC free article] [PubMed] [Google Scholar]
