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18 - A saltmarsh decomposition system and its ascomycetous laccase genes

from VI - Molecular ecology of fungi in the environment

Published online by Cambridge University Press:  03 November 2009

Steven Y. Newell
Affiliation:
The University of Georgia – Marine Institute
Justine I. Lyons
Affiliation:
The University of Georgia – Marine Institute
Mary Ann Moran
Affiliation:
The University of Georgia – Marine Institute
Geoffrey Gadd
Affiliation:
University of Dundee
Sarah C. Watkinson
Affiliation:
University of Oxford
Paul S. Dyer
Affiliation:
University of Nottingham
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Summary

Introduction

The saltmarshes of the Georgia, USA, Atlantic coast are expansive and highly productive. The marshes form the intertidal ecosystem 5–10 km wide extending from the barrier-island chain to the mainland. The predominant macrophyte of the marshes is smooth cordgrass (Spartina alterniflora Loisel.). Cross-marsh average annual production of smooth cordgrass shoots in Georgia has been measured at approximately 1.3 kg m− 2 of marsh (Newell, 2001a, from Dai & Wiegert, 1996). Like most grasses, smooth cordgrass does not abscise its leaf blades; they remain attached to the leaf sheath after senescence and death (Newell, 1993, and references therein). As new blades are produced at the apex of shoots, the bottom blades senesce and die, until the whole shoot dies after flowering. Therefore, a large crop of standing-dead litter is available to microbes for decomposition for much of the year (for leaf blades alone, up to 538 g dry mass m− 2) (Newell et al., 1998).

Because smooth cordgrass is produced in an intertidal marsh, one might suspect that tidal flooding would be a major wetting phenomenon for the standing-dead cordgrass leaves. However, the grass shoots extend above the flooding-tidal level most of the time: it is estimated that most of the dead-blade mass is wetted by tides only about 10% of the time on an annual-average basis (Newell et al., 1998).

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Publisher: Cambridge University Press
Print publication year: 2007

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References

Bergbauer, M. & Newell, S. Y. (1992). Contribution to lignocellulose degradation and DOC formation from a salt marsh macrophyte by the ascomycete Phaeosphaeria spartinicola. FEMS Microbiology Ecology 86, 341–8.CrossRefGoogle Scholar
Buchan, A., Newell, S. Y., Moreta, J. I. L. & Moran, M. A. (2002). Analysis of internal transcribed spacer (ITS) regions of rRNA genes in fungal communities in a southeastern U.S. salt marsh. Microbial Ecology 43, 329–40.CrossRefGoogle Scholar
Buchan, A., Newell, S. Y., Butler, M., Biers, E. J., Hollibaugh, J. T. & Moran, M. A. (2003). Dynamics of bacterial and fungal communities on decaying salt marsh grass. Applied and Environmental Microbiology 69, 6676–87.CrossRefGoogle ScholarPubMed
Dai, T. & Wiegert, R. G. (1996). Ramet population dynamics and net aerial primary productivity of Spartina alterniflora. Ecology 77, 276–88.CrossRefGoogle Scholar
Daniel, G., Volc, J., Kubatova, E. & Nilsson, T. (1992). Ultrastructural and immunocytochemical studies of the H2O2-producing enzyme pyranose oxidase in Phanerochaete chrysosporium grown under liquid culture conditions. Applied and Environmental Microbiology 58, 3667–76.Google Scholar
Eggert, C.Temp, U. & Eriksson, K.-E. (1997). Laccase is essential for lignin degradation by the white-rot fungus Pycnoporus cinnabarinus. FEBS Letters 407, 89–92.CrossRefGoogle ScholarPubMed
Graça, M. A., Newell, S. Y. & Kneib, R. T. (2000). Grazing rates of organic matter and living fungal biomass of decaying Spartina alterniflora by three species of salt-marsh invertebrates. Marine Biology 136, 281–9.Google Scholar
Hodson, R. E., Christian, R. R. & Maccubbin, A. E. (1984). Lignocellulose and lignin in the salt marsh grass Spartina alterniflora: initial concentrations and short-term, post-depositional changes in detrital matter. Marine Biology 81, 1–7.CrossRefGoogle Scholar
Johannes, C. & Majcherczyk, A. (2000). Natural mediators in the oxidation of polycyclic aromatic hydrocarbons by laccase mediator systems. Applied and Environmental Microbiology 66, 524–8.CrossRefGoogle ScholarPubMed
Kohlmeyer, J.& Kohlmeyer, E. (1979). Marine Mycology. The Higher Fungi. New York: Academic Press.Google Scholar
Kohlmeyer, J. & Volkmann-Kohlmeyer, B. (2003). Octopodotus stupendus gen. & sp. nov. and Phyllachora paludicola sp. nov., two marine fungi from Spartina alterniflora. Mycologia 95, 117–23.CrossRefGoogle ScholarPubMed
Lyons, J. I. (2002). Diversity of ascomycete laccase sequences and contributions of bacteria and ascomycetous fungi to lignocellulose degradation in a southeastern U.S. salt marsh. Master's Thesis, University of Georgia, Athens, GA, USA.
Lyons, J. I., Newell, S. Y., Buchan, A. & Moran, M. A. (2003). Diversity of ascomycete laccase gene sequences in a southeastern US salt marsh. Microbial Ecology 45, 207–81.CrossRefGoogle Scholar
Newell, S. Y. (1993). Decomposition of shoots of a saltmarsh grass. Advances in Microbial Ecology 13, 301–26.CrossRefGoogle Scholar
Newell, S. Y. (1995). Minimizing ergosterol loss during preanalytical handling and shipping of samples of plant litter. Applied and Environmental Microbiology 61, 2794–7.Google ScholarPubMed
Newell, S. Y. (1996). Established and potential impacts of eukaryotic mycelial decomposers in marine/terrestrial ecotones. Journal of Experimental Marine Biology and Ecology 200, 187–206.CrossRefGoogle Scholar
Newell, S. Y. (2001a). Multiyear patterns of fungal biomass dynamics and productivity within naturally decaying smooth cordgrass shoots. Limnology and Oceanography 46, 573–83.CrossRefGoogle Scholar
Newell, S. Y. (2001b). Spore-expulsion rates and extents of blade occupation by ascomycetes of the smooth-cordgrass standing-decay system. Botanica Marina 44, 277–85.CrossRefGoogle Scholar
Newell, S. Y. (2002). Fungi in marine/estuarine waters. In The Encyclopedia of Environmental Microbiology, ed. Bitton, G., pp. 1394–400. New York: Wiley.Google Scholar
Newell, S. Y. (2007). Evolution at the Marine Institute of the story of the fate of smooth cordgrass shoots, 1979–2002. In The University of Georgia Marine Institute – Five Decades of Research on Georgia's Coast, ed. Kneib, R. T., in press. Athens, GA: University of Georgia Press.Google Scholar
Newell, S. Y. & Porter, D. (2000). Microbial secondary production from saltmarsh-grass shoots, and its known and potential fates. In Concepts and Controversies in Tidal Marsh Ecology, ed. Weinstein, M. P. & Kreeger, D. A., pp. 159–85. Dordrecht: Kluwer Academic.CrossRefGoogle Scholar
Newell, S. Y., Fallon, R. D. & Miller, J. D. (1989). Decomposition and microbial dynamics for standing, naturally positioned leaves of the salt-marsh grass Spartina alterniflora. Marine Biology 101, 471–81.CrossRefGoogle Scholar
Newell, S. Y., Porter, D. & Lingle, W. L. (1996). Lignocellulolysis by ascomycetes (fungi) of a saltmarsh grass (smooth cordgrass). Microscopy Research and Technique 33, 32–46.3.0.CO;2-2>CrossRefGoogle Scholar
Newell, S. Y., Arsuffi, T. L. & Palm, L. A. (1998). Seasonal and vertical demography of dead portions of shoots of smooth cordgrass in a south-temperate saltmarsh. Aquatic Botany 60, 325–35.CrossRefGoogle Scholar
Nilsson, T., Daniel, G., Kirk, T. K. & Obst, J. R. (1989). Chemistry and microscopy of wood decay by some higher ascomycetes. Holzforschung 43, 11–18.CrossRefGoogle Scholar
Sarma, V. V., Newell, S. Y. & Hyde, K. D. (2001). Koorchaloma spartinicola sp. nov., a new sporodochial fungus from Spartina alterniflora. Botanica Marina 44, 321–6.CrossRefGoogle Scholar
Sinsabaugh, R. L. & Liptak, M. A. (1997). Enzymatic conversion of plant biomass. In The Mycota, vol. IV, Environmental and Microbial Relationships, ed. Wicklow, D. T. & Söderström, B., pp. 347–57. Berlin: Springer-Verlag.Google Scholar
Temp, U. & Eggert, C. (1999). Novel interaction between laccase and cellobiose dehydrogenase during pigment synthesis in the white rot fungus Pycnoporus cinnabarinus. Applied and Environmental Microbiology 65, 389–95.Google ScholarPubMed
Thurston, C. F. (1994). The structure and function of fungal laccases. Microbiology 140, 19–26.CrossRefGoogle Scholar
White, D. S. & Howes, B. L. (1994). Nitrogen incorporation into decomposing litter of Spartina alterniflora. Limnology and Oceanography 39, 133–40.CrossRefGoogle Scholar

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