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Philosophical Transactions of the Royal Society B: Biological Sciences logoLink to Philosophical Transactions of the Royal Society B: Biological Sciences
. 2000 Jun 29;355(1398):833–846. doi: 10.1098/rstb.2000.0618

Land plant biochemistry.

J A Raven 1
PMCID: PMC1692786  PMID: 10905612

Abstract

Biochemical studies have complemented ultrastructural and, subsequently molecular genetic evidence consistent with the Charophyceae being the closest extant algal relatives of the embryophytes. Among the genes used in such molecular phylogenetic studies is that rbcL) for the large subunit of ribulose bisphosphate carboxylase-oxygenase (RUBISCO). The RUBISCO of the embryophytes is derived, via the Chlorophyta. from that of the cyanobacteria. This clade of the molecular phylogeny of RUBISCO shows a range of kinetic characteristics, especially of CO2 affinities and of CO2/O2 selectivities. The range of these kinetic values within the bryophytes is no greater than in the rest of the embryophytes; this has implications for the evolution of the embryophytes in the high atmospheric CO2 environment of the late Lower Palaeozoic. The differences in biochemistry between charophycean algae and embryophytes can to some extent be related functionally to the structure and physiology of embryophytes. Examples of components of embryophytes, which are qualitatively or quantitatively different from those of charophytes, are the water repellent/water resistant extracellular lipids, the rigid phenolic polymers functional in water-conducting elements and mechanical support in air, and in UV-B absorption, flavonoid phenolics involved in UV-B absorption and in interactions with other organisms, and the greater emphasis on low Mr organic acids. retained in the plant as free acids or salts, or secreted to the rhizosphere. The roles of these components are discussed in relation to the environmental conditions at the time of evolution of the terrestrial embryophytes. A significant point about embryophytes is the predominance of nitrogen-free extracellular structural material (a trait shared by most algae) and UV-B screening components, by contrast with analogous components in many other organisms. An important question, which has thus far been incompletely addressed, is the extent to which the absence from bryophytes of the biochemical pathways which produce components found only in tracheophytes is the result of evolutionary loss of these functions.

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Selected References

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  1. Berner R. A., Canfield D. E. A new model for atmospheric oxygen over Phanerozoic time. Am J Sci. 1989 Apr;289(4):333–361. doi: 10.2475/ajs.289.4.333. [DOI] [PubMed] [Google Scholar]
  2. Lindahl T. The Croonian Lecture, 1996: endogenous damage to DNA. Philos Trans R Soc Lond B Biol Sci. 1996 Nov 29;351(1347):1529–1538. doi: 10.1098/rstb.1996.0139. [DOI] [PubMed] [Google Scholar]
  3. Logan G. A., Boon J. J., Eglinton G. Structural biopolymer preservation in Miocene leaf fossils from the Clarkia site, northern Idaho. Proc Natl Acad Sci U S A. 1993 Mar 15;90(6):2246–2250. doi: 10.1073/pnas.90.6.2246. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Lorimer G. H., Chen Y. R., Hartman F. C. A role for the epsilon-amino group of lysine-334 of ribulose-1,5-bisphosphate carboxylase in the addition of carbon dioxide to the 2,3-enediol(ate) of ribulose 1,5-bisphosphate. Biochemistry. 1993 Sep 7;32(35):9018–9024. doi: 10.1021/bi00086a006. [DOI] [PubMed] [Google Scholar]
  5. Ludwig M, von Caemmerer S, Dean Price G, Badger MR, Furbank RT. Expression of tobacco carbonic anhydrase in the C4 dicot flaveria bidentis leads to increased leakiness of the bundle sheath and a defective CO2-concentrating mechanism . Plant Physiol. 1998 Jul;117(3):1071–1081. doi: 10.1104/pp.117.3.1071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Maathuis F. J., Sanders D. Mechanism of high-affinity potassium uptake in roots of Arabidopsis thaliana. Proc Natl Acad Sci U S A. 1994 Sep 27;91(20):9272–9276. doi: 10.1073/pnas.91.20.9272. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. doi: 10.1098/rstb.1998.0197. [DOI] [PMC free article] [Google Scholar]
  8. doi: 10.1098/rstb.1998.0187. [DOI] [PMC free article] [Google Scholar]
  9. doi: 10.1098/rstb.1998.0192. [DOI] [PMC free article] [Google Scholar]
  10. Pearson PN, Palmer MR. Middle eocene seawater pH and atmospheric carbon dioxide concentrations . Science. 1999 Jun 11;284(5421):1824–1826. doi: 10.1126/science.284.5421.1824. [DOI] [PubMed] [Google Scholar]
  11. Watson G. M., Tabita F. R. Microbial ribulose 1,5-bisphosphate carboxylase/oxygenase: a molecule for phylogenetic and enzymological investigation. FEMS Microbiol Lett. 1997 Jan 1;146(1):13–22. doi: 10.1111/j.1574-6968.1997.tb10165.x. [DOI] [PubMed] [Google Scholar]
  12. Yeoh H. H., Badger M. R., Watson L. Variations in Kinetic Properties of Ribulose-1,5-bisphosphate Carboxylases among Plants. Plant Physiol. 1981 Jun;67(6):1151–1155. doi: 10.1104/pp.67.6.1151. [DOI] [PMC free article] [PubMed] [Google Scholar]

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