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271Use of white rot fungi to improve the feed value of rice strawJ W Cone 1 , J J P Baars 2 , A S M Sonnenberg 21 Animal Nutrition Group, Wageningen University, Wageningen, Netherlands, 2 Plant Sciences Group, Wageningen,NetherlandsEmail: john.cone@wur.nlIntroduction In many countries straw is a main feed for cattle in the winter or in the dry season. However, the feed valueof straw is too low to obtain high production levels. One of the main reason for the low feed value of straw is the highlignin level (for rice straw up to 5 %), preventing microbes to access the valuable carbohydrates and causing a low feedintake. In the past many attempts have been published to increase the feed value, using sodium hydroxide, urea andammonia. Rodrigues et al. (2008) showed that enzymes of fungi are capable of increasing the digestibility of straw inrumen fluid. The aim of the present research was in investigate if growing fungi can be used to unseal the straw and toincrease its feed value. Rice straw samples were incubated for different periods with two strains of white rot fungi beforebeing fermented in rumen fluid, using the gas production technique.Material and methods Rice straw from Thailand was chopped to pieces of 3 cm. The white rot fungi Pleurotus ostreatusand Volvariella volvacea were inoculated for 6 days on 2% malt agar disks (diameter, 7-8 mm) at 24 ºC. Each 20 grams ofchopped rice straw samples were put into 1000 ml Erlenmeyer flasks with 80 ml of distilled water. The flasks wereautoclaved at 121 ºC for 30 min and, aftercooling, three agar disks of each fungus culture 280were added aseptically and incubated at 24 ºC 260for 0 to 35 days. Three replications for eachA240fungus culture of each incubation period were220used. After incubation the rice straw sampleswere freeze dried, ground to 1 mm and analysed 200for fermentability in rumen fluid. Gas production 180incubations were performed as described by160Cone et al. (1996), using rumen fluid from 2 non140lactating Holstein Friesian cows receiving 1 kgof concentrate and ad libitum grass silage.120Results Figure 1a shows the gas production (mlgas/g OM), caused by fermentation of the nonsolublefraction (A2) of the straw samples afterincubation with the white rot fungi P. ostreatusand V. volvacea for different periods (days).Figure 1b shows the half time to reach A2 (B2),which is an indication of the rate of fermentationof the non-soluble fraction, in this case NDF. Alower value of B2 means an increased rate offermentation. The results show that prolongedincubation with V. volvacea results in a lowerfermentation of the NDF (decreased A2) and aslower rate of fermentation (increased B2),indicating that during the incubation of the strawwith the fungus, V. volvacea used the most easilydigestible parts of the straw, remaining less forthe rumen microbes. The same was seen forstraw samples incubated with P. ostreatus up to14 days. Incubating the straw for a prolongedperiod with this fungus resulted in an increasedfermentation of the NDF in rumen fluid with anincreased rate. This indicates that initially P.A2 (ml gas/g OM)B2 (h)100201918171615141312C P7 P14 P21 P28 P35 C V7 V14 V21 V28 V35C P7 P14 P21 P28 P35 C V7 V14 V21 V28 V35Figure 1 (a) Gas production (A2, ml gas/g OM) of the non-solublefraction and (b) time to reach half of A2 (B2, h) of untreated ricestraw (C) and straw incubated for 7 to 35 days with the white rotfungi Pleurotis ostreatis (P) and Volvariella volvacea (V).ostreatus also used easy assessable carbohydrates, but after 2 weeks the fungus used the difficult degradable components,most likely lignin, increasing the degradability of the straw in rumen fluid.Conclusions The results show that a prolonged incubation of rice straw with the white rot fungus P. ostreatus increases itsfeed value for ruminants.ReferencesCone, J.W., Van Gelder, A.H., Visscher, G.J.W. and Oudshoorn, L. 1996. Animal Feed Science and Technology 61, 113-128.Rodrigues, M.A.M., Pinto, P., Bezerra, R.M.F., Dias, A.A., Guedes, C.V.M., Cardoso, V.M.G., Cone, J.W., Ferreira,L.M.M., Colaço, J., Sequeira, C.A. (2008) Animal Feed Science and Technology 141, 326-338.B

271<strong>Use</strong> <strong>of</strong> <strong>white</strong> <strong>rot</strong> <strong>fungi</strong> <strong>to</strong> <strong>improve</strong> <strong>the</strong> <strong>feed</strong> <strong>value</strong> <strong>of</strong> rice strawJ W Cone 1 , J J P Baars 2 , A S M Sonnenberg 21 Animal Nutrition Group, <strong>Wageningen</strong> University, <strong>Wageningen</strong>, Ne<strong>the</strong>rlands, 2 Plant Sciences Group, <strong>Wageningen</strong>,Ne<strong>the</strong>rlandsEmail: john.cone@wur.nlIntroduction In many countries straw is a main <strong>feed</strong> for cattle in <strong>the</strong> winter or in <strong>the</strong> dry season. However, <strong>the</strong> <strong>feed</strong> <strong>value</strong><strong>of</strong> straw is <strong>to</strong>o low <strong>to</strong> obtain high production levels. One <strong>of</strong> <strong>the</strong> main reason for <strong>the</strong> low <strong>feed</strong> <strong>value</strong> <strong>of</strong> straw is <strong>the</strong> highlignin level (for rice straw up <strong>to</strong> 5 %), preventing microbes <strong>to</strong> access <strong>the</strong> valuable carbohydrates and causing a low <strong>feed</strong>intake. In <strong>the</strong> past many attempts have been published <strong>to</strong> increase <strong>the</strong> <strong>feed</strong> <strong>value</strong>, using sodium hydroxide, urea andammonia. Rodrigues et al. (2008) showed that enzymes <strong>of</strong> <strong>fungi</strong> are capable <strong>of</strong> increasing <strong>the</strong> digestibility <strong>of</strong> straw inrumen fluid. The aim <strong>of</strong> <strong>the</strong> present research was in investigate if growing <strong>fungi</strong> can be used <strong>to</strong> unseal <strong>the</strong> straw and <strong>to</strong>increase its <strong>feed</strong> <strong>value</strong>. Rice straw samples were incubated for different periods with two strains <strong>of</strong> <strong>white</strong> <strong>rot</strong> <strong>fungi</strong> beforebeing fermented in rumen fluid, using <strong>the</strong> gas production technique.Material and methods Rice straw from Thailand was chopped <strong>to</strong> pieces <strong>of</strong> 3 cm. The <strong>white</strong> <strong>rot</strong> <strong>fungi</strong> Pleu<strong>rot</strong>us ostreatusand Volvariella volvacea were inoculated for 6 days on 2% malt agar disks (diameter, 7-8 mm) at 24 ºC. Each 20 grams <strong>of</strong>chopped rice straw samples were put in<strong>to</strong> 1000 ml Erlenmeyer flasks with 80 ml <strong>of</strong> distilled water. The flasks wereau<strong>to</strong>claved at 121 ºC for 30 min and, aftercooling, three agar disks <strong>of</strong> each fungus culture 280were added aseptically and incubated at 24 ºC 260for 0 <strong>to</strong> 35 days. Three replications for eachA240fungus culture <strong>of</strong> each incubation period were220used. After incubation <strong>the</strong> rice straw sampleswere freeze dried, ground <strong>to</strong> 1 mm and analysed 200for fermentability in rumen fluid. Gas production 180incubations were performed as described by160Cone et al. (1996), using rumen fluid from 2 non140lactating Holstein Friesian cows receiving 1 kg<strong>of</strong> concentrate and ad libitum grass silage.120Results Figure 1a shows <strong>the</strong> gas production (mlgas/g OM), caused by fermentation <strong>of</strong> <strong>the</strong> nonsolublefraction (A2) <strong>of</strong> <strong>the</strong> straw samples afterincubation with <strong>the</strong> <strong>white</strong> <strong>rot</strong> <strong>fungi</strong> P. ostreatusand V. volvacea for different periods (days).Figure 1b shows <strong>the</strong> half time <strong>to</strong> reach A2 (B2),which is an indication <strong>of</strong> <strong>the</strong> rate <strong>of</strong> fermentation<strong>of</strong> <strong>the</strong> non-soluble fraction, in this case NDF. Alower <strong>value</strong> <strong>of</strong> B2 means an increased rate <strong>of</strong>fermentation. The results show that prolongedincubation with V. volvacea results in a lowerfermentation <strong>of</strong> <strong>the</strong> NDF (decreased A2) and aslower rate <strong>of</strong> fermentation (increased B2),indicating that during <strong>the</strong> incubation <strong>of</strong> <strong>the</strong> strawwith <strong>the</strong> fungus, V. volvacea used <strong>the</strong> most easilydigestible parts <strong>of</strong> <strong>the</strong> straw, remaining less for<strong>the</strong> rumen microbes. The same was seen forstraw samples incubated with P. ostreatus up <strong>to</strong>14 days. Incubating <strong>the</strong> straw for a prolongedperiod with this fungus resulted in an increasedfermentation <strong>of</strong> <strong>the</strong> NDF in rumen fluid with anincreased rate. This indicates that initially P.A2 (ml gas/g OM)B2 (h)100201918171615141312C P7 P14 P21 P28 P35 C V7 V14 V21 V28 V35C P7 P14 P21 P28 P35 C V7 V14 V21 V28 V35Figure 1 (a) Gas production (A2, ml gas/g OM) <strong>of</strong> <strong>the</strong> non-solublefraction and (b) time <strong>to</strong> reach half <strong>of</strong> A2 (B2, h) <strong>of</strong> untreated ricestraw (C) and straw incubated for 7 <strong>to</strong> 35 days with <strong>the</strong> <strong>white</strong> <strong>rot</strong><strong>fungi</strong> Pleu<strong>rot</strong>is ostreatis (P) and Volvariella volvacea (V).ostreatus also used easy assessable carbohydrates, but after 2 weeks <strong>the</strong> fungus used <strong>the</strong> difficult degradable components,most likely lignin, increasing <strong>the</strong> degradability <strong>of</strong> <strong>the</strong> straw in rumen fluid.Conclusions The results show that a prolonged incubation <strong>of</strong> rice straw with <strong>the</strong> <strong>white</strong> <strong>rot</strong> fungus P. ostreatus increases its<strong>feed</strong> <strong>value</strong> for ruminants.ReferencesCone, J.W., Van Gelder, A.H., Visscher, G.J.W. and Oudshoorn, L. 1996. Animal Feed Science and Technology 61, 113-128.Rodrigues, M.A.M., Pin<strong>to</strong>, P., Bezerra, R.M.F., Dias, A.A., Guedes, C.V.M., Cardoso, V.M.G., Cone, J.W., Ferreira,L.M.M., Colaço, J., Sequeira, C.A. (2008) Animal Feed Science and Technology 141, 326-338.B


Proceedings<strong>of</strong> <strong>the</strong> British Society <strong>of</strong> Animal Scienceand <strong>the</strong> Agricultural Research Forum2010Advances in Animal BiosciencesThis book is part <strong>of</strong> a series which is a companion <strong>to</strong> <strong>the</strong> journal ANIMAL


The Proceedings <strong>of</strong> <strong>the</strong> British Society <strong>of</strong> Animal Scienceconstitute summaries <strong>of</strong> papers presented at <strong>the</strong> Society'sAnnual Conference in Belfast, UK, 12-14 April 2010.The meeting was organised jointly with <strong>the</strong> AgriculturalResearch Forum whose papers are incorporated.The summaries have been edited. Views expressed in allcontributions are those <strong>of</strong> <strong>the</strong> authors and not those <strong>of</strong><strong>the</strong> British Society <strong>of</strong> Animal Science or <strong>the</strong> AgriculturalResearch Forum.This publication contains all <strong>the</strong> summaries that wereavailable at <strong>the</strong> time <strong>of</strong> going <strong>to</strong> press.Edi<strong>to</strong>rsS AthanasiadouE M BaxterD P BerryD Bol<strong>to</strong>nA F CarsonM A CroweL DawsonM G DiskinP D ForristalC E HaleJ P HanrahanM HazzledineL HeasmanN M HoldenD A KennyR W MayesT McCabeA P MoloneyD M NashP O’KielyK G RichardsR I RichardsonJ A RookeM RoseC RymerM A SteeleE WallM WallaceB T WolfB Younge© 2010 British Society <strong>of</strong> Animal ScienceISBN 978-0-906562-67-3ISSN 2040-4700

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