Degradation of low rank coal by Trichoderma atroviride ES11

A new isolate of Trichoderma atroviride has been shown to grow on low rank coal as the sole carbon source. T. atroviride ES11 degrades ~82% of particulate coal (10 g l-¹) over a period of 21 days with 50% reduction in 6 days. Glucose (5 g l-¹) as a supplemented carbon source enhanced the coal solubi...

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Veröffentlicht in:Journal of industrial microbiology & biotechnology 2007-09, Vol.34 (9), p.625-631
Hauptverfasser: Silva-Stenico, M. Estela, Vengadajellum, Caryn J, Janjua, Hussnain A, Harrison, Sue T. L, Burton, Stephanie G, Cowan, Don A
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Sprache:eng
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Zusammenfassung:A new isolate of Trichoderma atroviride has been shown to grow on low rank coal as the sole carbon source. T. atroviride ES11 degrades ~82% of particulate coal (10 g l-¹) over a period of 21 days with 50% reduction in 6 days. Glucose (5 g l-¹) as a supplemented carbon source enhanced the coal solubilisation efficiency of T. atroviride ES11, while 10 and 20 g l-¹ glucose decrease coal solubilisation efficiency. Addition of nitrogen [1 g l-¹ (NH₄)₂SO₄] to the medium also increased the coal solubilisation efficiency of T. atroviride ES11. Assay results from coal-free and coal-supplemented cultures suggested that several intracellular enzymes are possibly involved in coal depolymerisation processes some of which are constitutive (phenol hydroxylase) and others that were activated or induced in the presence of coal (2,3-dihydrobiphenyl-2,3-diol dehydrogenase, 3,4-dihydro phenanthrene-3,4-diol dehydrogenase, 1,2-dihydro-1,2-dihydroxynaphthalene dehydrogenase, 1,2-dihydro-1,2-dihydroxyanthracene dehydrogenase). GC-MS analysis of chloroform extracts obtained from coal degrading T. atroviride ES11 cultures showed the formation of only a limited number of specific compounds (4-hydroxyphenylethanol, 1,2-benzenediol, 2-octenoic acid), strongly suggesting that the intimate association between coal particles and fungal mycelia results in rapid and near-quantitative transfer of coal depolymerisation products into the cell.
ISSN:1367-5435
1476-5535
DOI:10.1007/s10295-007-0223-7