2008
DOI: 10.1016/j.bej.2008.06.006
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Production of lignin modifying enzymes on industrial waste material by solid-state cultivation of fungi

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Cited by 63 publications
(31 citation statements)
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References 35 publications
(37 reference statements)
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“…Solid state cultivation on lignocellulose is often suitable for the production of LiP and MnP [42], but it was not superior in our study. However, the enzyme activities in the extracts are difficult to directly compare with the liquid culture supernatants because the mycelial growth is different in solid medium but also because the activity was calculated on the basis of liquid extracted, here 4 g oat husk medium extracted with 16 ml buffer [35], not on the culture filtrates of liquid cultures, which contain less but more easily digestible carbon sources. The use of more nutrient rich media in screening allowed the expression of lignin-modifying peroxidases in many fungi, but apparently the production of LiP was promoted by nutrient poor medium.…”
Section: Production Of Lignin-modifying Peroxidasesmentioning
confidence: 99%
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“…Solid state cultivation on lignocellulose is often suitable for the production of LiP and MnP [42], but it was not superior in our study. However, the enzyme activities in the extracts are difficult to directly compare with the liquid culture supernatants because the mycelial growth is different in solid medium but also because the activity was calculated on the basis of liquid extracted, here 4 g oat husk medium extracted with 16 ml buffer [35], not on the culture filtrates of liquid cultures, which contain less but more easily digestible carbon sources. The use of more nutrient rich media in screening allowed the expression of lignin-modifying peroxidases in many fungi, but apparently the production of LiP was promoted by nutrient poor medium.…”
Section: Production Of Lignin-modifying Peroxidasesmentioning
confidence: 99%
“…The media were a) low nitrogen (2 mM) asparagine-dimethyl succinate-medium (M), containing 0.5% (w/v) glucose, pH 4.5 [23], b) peptone medium (P) with yeast extract 0.2% (w/v), peptone 0.5% (w/v), glucose 2% (w/v), 7 mM KH2PO4, 2 mM MgSO4 and 100 µM MnSO4, pH 5 (modified from [34]), c) soy medium (S) with 2% (w/v) soy briquettes (Mildola Ltd, Kirkkonummi, Finland), water, pH adjusted to 5, and d) solid oat husk (Rapion Tuote Inc., Finland) medium (O) with water supplementation [35]. For the production of inocula fungi were cultivated in 2% (w/v) malt extract medium and the mycelium with the medium was homogenized in a Waring blender four times 10 sec in 30 sec intervals.…”
Section: Culture Conditionsmentioning
confidence: 99%
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“…evolution from 14 C-[Ring]-labelled synthetic lignin (DHP) (13,35). In order to depolymerize and mineralize lignin, they have developed an oxidative and unspecific system including extracellular enzymes, low molecular weight metabolites and activated oxygen species (28,29).…”
Section: Co2mentioning
confidence: 99%
“…Despite relatively long incubation times, SSF offers an inexpensive and effective means of fungal cultivation that can also be used for the production of potentially valuable fungal enzymes [79][80][81]. Fungal enzymes produced by SSF have been used to enhance methane production by anaerobic digestion [82].…”
Section: Species and Systems Investigatedmentioning
confidence: 99%