Rumen Microbial Tolerance to The Use of Jatropha curcas Meal

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    RUMEN MICROBIAL

    TOLERANCE TO THE USEOF Jatropha curcasMEAL

    Ir. Anita S. Tjakradidjaja, MRur.Sc.Dr. Ir. Komang G. Wiryawan

    Azimatul Ulya, SPt.

    Faculty of Animal Science

    Bogor Agricultural University

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    INTRODUCTION

    1. Limitation in availability of fossil fuel searching other

    sources : oil produced from non-edible plants

    JatrophacurcasL. = biodiesel

    2. Byproducts of oil extraction seed meal (seed cake)

    1 ton/ha byproduct from 5 ton seed/ha = potential in its

    production (Makkar & Becker, 2000)3. Nutrient content : depend on inclusion of seed coat during

    oil extraction

    1. without seed coat high CP & EE contents, low CF content

    2. with seed coat lower CP & EE contents, higher CF content

    = potential use as protein supplement

    4. Limitations : antinutrients/toxins : curcin & phorbolester

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    Table 1. Nutrient composition J. curcas

    Nutrient Without

    seed coat

    With

    seed coat

    Seed coat

    Dry matter (%) 86.26 89.71 88.31

    Ash (%) 7.71 5.20 4.22

    Crude prot. (%) 37.56 24.28 10.21

    Ether extrt. (%) 35.02 15.99 5.71

    Crude fibr. (%) 7.23 38.49 59.62

    N free extr. (%) 12.47 16.06 20.24

    NDF (%) 16.30 57.64 93.40ADF (%) 15.86 46.78 80.90

    Lignin (%) 4.51 23.98 46.00

    Tjakradidjaja et al. (2007)

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    Table 2. Antinutrients in J. curcas

    Antinutrients Toxic variety Non toxic variety

    Phorbolester (mg/g kernel) 2.79 0.11

    Total phenols

    (% tannic acid equiv)

    0.36 0.22

    Tannin (% tannic acid equiv) 0.04 0.02

    Phytat (% DM) 9.40 8.90

    Saponin (% diosgenin equiv) 2.60 3.40

    Trypsin inhibtr (mg trpsininhibited/g sample)

    21.3 26.5

    Lektin (1/mg substance causinghemaglutination/ml mediumassay)

    102 51

    Makkar et al. (1998)

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    5. Ruminants :

    1. microbes in rumen able to degrade CF bacteria & fungi

    2. ability to degrade CF varies among microbes & ruminantsadaptation to feed

    6. Also differ in degrading antinutrients/toxins presence in feed1. mimosine S. jonesii rumen bacterium degrading mimosine

    - overcoming problem of mimosine toxicity

    2. other antinutrients : tannin & DABA3. adaptation to feed - important

    4. possible also occur to antinutrients/toxins from J. curcasmeal

    Aim of experimentTo study tolerance of rumen microbes from differentruminants to J. curcas antinutrients/toxins

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    MATERIALS & METHODS

    Treatments :

    1. Faktor A : Rumen fluid sources - 4Cattle, Buffalo, Goat & Sheep

    2. Faktor B : Incubation period 50, 3, 6, 9, & 12

    Experimental design :

    Factorial randomised block design 4 x 5Rumen fluids from 3 animals for each species = block

    Data analysis : Anova & Contrast Orthogonal Variables

    1. Fermentability Tilley & Terry method (1963) Sutardi (1979)

    [NH3] microdiffusion Conway; [VFA] steam distillation2. Bacterial & protozoal populations Ogimoto & Imai (1981)

    3. DM & OM degradabilities Tilley & Terry method (1963) Sutardi (1979) proximate analysis DM & OM content

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    Prosedur :

    - Fermentability study

    1. mix ground feed sample (1 g) + buffer soln (12 ml) + RF (8 ml)2. put in fermentor tube & gas with CO2 (anerob)

    3. incubate in shaker bath at 39 oC 0, 3, 6, 9 & 12 h

    4. take sample for bacterial & protozoal population

    5. stop fermentation (+ HgCl2)

    6. centrifuge 3 000 rpm 10 min

    7. take supernatant for determining [NH3] & [VFA]

    1. [NH3] microdiffusion Conway

    2. [VFA] steam distillation

    8. use residue for analysing DM and OM contents1. DM content oven 105 oC 24 h

    2. OM content ash content furnace oven 600 oC 6 8 h

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    RESULTS & DISCUSSION

    Effects of treatment factors :

    1. Rumen fluid sources

    1. Highly significant (P

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    Table 3. Effects of rumen fluid source

    Variable Cattle Buffalo Goat Sheep Anova

    [NH3] mM 10.58B 13.77B 27.11A 12.74B (P

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    Table 4. Effects of incubation period

    Variable 0 h 3 h 6 h 9 h 12 h

    [NH3] mM 10.21Bc 15.74Bb 16.91Aa 17.46Aa 20.27Aa

    [VFA] mM 119.47 122.59 107.48 111.39 118.90

    Bac. No.x 1012 CFU/ml

    Amylolytc 2.05 1.57 1.24 1.10 1.42

    Cellolytc 1.07 0.88 0.93 1.75 1.09

    Prteolytc 2.88 4.00 3.76 3.82 4.04

    Prto. No.

    x 104 sel/ml

    0.68 0.62 0.44 0.57 0.49

    DM deg(%)

    8.87B 9.03B 11.54A 11.40A 13.73A

    OM deg(%)

    11.41B 10.34B 15.11A 13.74A 16.84A

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    CONCLUSION

    Use of J. curcasmeal affected [NH3

    ] & [VFA],proteolytic bacterial & protozoal populations

    The highest rslts obtained from degradation of J.curcas meal with rumen fluids of goat

    No different among rumen fluids of cattle, bufallo &sheep in all variables

    Microbes from rumen fluids of goats = moretolerant to antinutrients of J. curcasmeal

    Optimum degradation of J. curcasmeal = 6 hincubation period the highest [NH3] & DM & OMdegradability