Rumen Fluids

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H J Yang - One of the best experts on this subject based on the ideXlab platform.

  • effect of urea fertilization on biomass yield chemical composition in vitro Rumen digestibility and fermentation characteristics of forage oat straw in tibet of china
    The Journal of Agricultural Science, 2016
    Co-Authors: J H Cui, H J Yang, S Bai, S S Song, Wei Sun, X M Shao, L S Jiang
    Abstract:

    The present study investigated the effects of different levels of urea nitrogen (N) fertilizer on nutrient accumulation, in vitro Rumen gas production and fermentation characteristics of forage oat straw (FOS) from oats ( Avena sativa L. ‘Qinghai 444’) grown in the Tibet region of China. Fertilizer, applied at seeding (day 1), stem elongation (days 52–54) and heading (days 63–67), increased plant height and prolonged the maturity stage of the plant by 4–11 days compared with the non-fertilized control. Oat plants were harvested at maturity at the node 3–4 cm above ground, and then separated into grains and FOS. Both FOS and grain yields increased quadratically with increasing N fertilization, and their theoretical maximums occurred at the N fertilizing rates of 439 and 385 kg/ha, respectively. Increases in N fertilization did not affect the hemicellulose content of FOS, but substantially promoted the accumulation of crude protein, cellulose and lignin, resulting in a decrease in the energy content available for metabolism. A 72-h incubation of FOS with Rumen Fluids from lactating cows showed that increasing N resulted in FOS that showed a slower fermentation rate, decreased in vitro dry matter disappearance and lower cumulative gas production, but unchanged fermentation gas composition. Nitrogen fertilization increased the final pH in culture Fluids and decreased the microbial volatile fatty acid (VFA) production. The molar proportions of acetate and propionate were not affected, but molar propionate proportion decreased linearly with increasing urea fertilization, and consequently, the ratio of lipogenic (e.g., acetate and butyrate)-to-glucogenic acids (propionate) tended to increase. In brief, increasing urea N fertilization promoted the growth of forage oats and increased the biomass yield as well as the crude protein and cellulose content of FOS. Considering the negative effect of increased lignin content on nutrient digestibility and total VFA production, the suggested range of urea N fertilization is 156–363 kg N/ha for forage oats planted in Tibet to retain the nutritive value of FOS in the Rumen.

  • effect of roughage fibre content on fibrolytic activities and volatile fatty acid profiles of neocallimastix sp yak11 isolated from Rumen Fluids of yak bos grunniens
    Animal Feed Science and Technology, 2011
    Co-Authors: Yunhe Cao, H J Yang
    Abstract:

    A 10-day pure culture of Neocallimastix sp. YAK11, isolated from Rumen Fluids of yak (Bos grunniens) was evaluated for fibrolytic activity, apparent dry matter disappearance (ADMD), ferulic acid, reducing sugars and volatile fatty acids (VFA). The fungus was grown on oat straw (OS), corn stalks (CS), rice straw (RS) and wheat straw (WS). Recovered activity of ferulic acid esterase peaked at day 5 in all roughages, and the lowest activity was found with low fibre OS throughout the incubation (P 0.42, P<0.01). Molar proportions of acetate and valerate did not differ in the roughages. The lowest propionate and branch chained VFA levels occurred in WS (P=0.0115), and the highest butyrate levels occurred in OS throughout the 10-d incubation (P=0.0464). The highest ratio of non-glucogenic to glucogenic acids (NGR) occurred in WS (P=0.0481). NGR peaked for all roughages around day 3 and then slightly declined for the rest of the experiment. In general, the isolate was capable of a pronounced degradation that would depend on the fibre content of the roughages. Screening of fungi from Rumen Fluids of yak would appear to be a useful strategy to obtain highly active esterases and polysaccharide hydrolases.

  • effects of crude feruloyl and acetyl esterase solutions of neocallimastix sp yq1 and anaeromyces sp yq3 isolated from holstein steers on hydrolysis of chinese wildrye grass hay wheat bran maize bran wheat straw and corn stalks
    Animal Feed Science and Technology, 2009
    Co-Authors: H J Yang, D F Zhang, J Q Wang
    Abstract:

    Abstract Neocallimastix sp. YQ1 and Anaeromyces sp. YQ3 were isolated from Rumen Fluids of Holstein steers using a modification of the roll-tube technique of Hungate (1969) . After a 9-day incubation for YQ1, and a 4-day incubation for YQ3, with optimal carbon and N supply in cultures, crude enzyme solutions of both fungi were prepared by centrifuging cultures for 10 min at 1000 ×  g at 4 °C. Enzymological characteristics of ferulic acid esterase and acetyl esterase were measured in the crude enzyme solution. The Michaelis constants ( K m ) and maximum velocities ( V max ) of ferulic acid esterase against methyl ferulate at pH 6.0 and 39 °C were 30 μM and 8.05 mU for YQ1 and 129 μM and 3.15 mU for YQ3, respectively. With substrate of p -nitrophenyl acetate, the K m and V max of AE at pH 6.0 and 39 °C were 0.21 mM and 336 mU for YQ1 and 5.26 mM and 854 mU for YQ3. Enzymatic release of reducing sugar, ferulic acid, and p -coumaric acid from complex fibre-rich feedstuffs was evaluated, and YQ3 released more reducing sugars from wheat straw, but less from the other plant materials especially maize bran and corn stalks. YQ3 liberated much more hydroxycinnamic acids from corn stalks, and YQ1 liberated much more hydroxycinnamic acids from maize bran. Anaerobic Rumen fungi showed species diversity of enzymological characteristics of ferulic acid esterase and acetyl ester esterase, and exhibited a strong capability to release ferulic acid and p -coumaric acid from complex fibre-rich feedstuffs. Therefore anaerobic fungi, especially their FAE, should not be neglected in studies on biodegradation of plant cell walls in the Rumen as well as on industrial processes developed to release ferulic acid and p -coumaric acid from agricultural by-products with potential commercial industrial applications, such as precursors of natural vanillin, natural antioxidants, food preservative agents, anti-inflammatory agents and photoprotectants.

Retno Iswarin Pujaningsih - One of the best experts on this subject based on the ideXlab platform.

  • Perlindungan Protein Menggunakan Tanin dan Saponin Terhadap Daya Fermentasi Rumen dan Sintesis Protein Mikrob (PROTECTION OFPROTEINUSINGTANNINS AND SAPONINS OF Rumen DIGESTIBILITYAND MICROBESSYNTHESISPROTEIN)
    Universitas Udayana, 2015
    Co-Authors: Ana Shofi Ani, Retno Iswarin Pujaningsih
    Abstract:

    The objective of this experiment was to examine protection of protein using tannins and saponins toimprove Rumen digestibility and microb-mediated protein synthesis in vitro. Rumen Fluids used as inoculumwas collected from a composite of two female adult fistulatedongole cattle weighed of ±300 kg with theage of five years old. The experimental design used in this study was a completely randomized design withsix treatments and three replication of each treatment. The six treatments consisted of T0: Proteinconcentrates without protection, T1: protein concentrates protected with 1.2% saponin, T2: proteinconcentrates protected with 0.5% tannin and 0.9% saponin , T3: protein concentrates protected with 1.0%tannin and 0.6% saponin, T4: protein concentrates protected with 1.5 % tannin and 0.3% saponin and T5:protein concentrates protected with 2.0% tannins. The result showed that treatment with tannin, saponinand their combination had a significantly affect (P

  • Pengaruh Suplementasi dan Proteksi Minyak Biji Kapuk Terhadap Fermentabilitas Ruminal Rumput Gajah pada Sapi Secara In Vitro
    Syiah Kuala University, 2015
    Co-Authors: D. D. Dinata, Widiyanto Widiyanto, Retno Iswarin Pujaningsih
    Abstract:

    (The effect of supplementation and protection of kapok seed oil on in vitro ruminal fermentability of elephant grass)  ABSTRACT. The purpose of this research was to study the interaction between supplementation and protection of kapok seed oil (KSO) influence on in vitro digestibility and ruminal fermentability products of elephant grass.  Material used were elephant grass, kapok seed oil, KOH and CaCl2 reagens and cattle Rumen Fluids.  Completely randomized design (CRD) was used with two factorial pattern 3 x 5 with 2 replications, first factor was supplementation of KSO consist of 3 levels: 5% (S1); 10% (S2); and 15% (S3), respectively.  Second factor was protection consist of 5 levels: 0% (P0); 25% (P1); 50% (P2); 75% (P3) and 100% (P4); also control treatment without supplementation and protection of KSO (S0P0).  The result of this research showed there was no interaction between supplementation and protection of KSO on digestibility of elephant grass.  The highest In vitro Dry Matter Digestibility (IVDMD) and In vitro Digestibility of Organic Material (IVDOM) reached by control treatment, 55,17% and 54,27%, respectively.  The results of this research showed influence of interaction between supplementation and protection of KSO on VFA and NH3 production (P

  • Perlindungan Protein Menggunakan Tanin dan Saponin Terhadap Daya Fermentasi Rumen dan Sintesis Protein Mikrob (PROTECTION OFPROTEINUSINGTANNINS AND SAPONINS OF Rumen DIGESTIBILITYAND MICROBESSYNTHESISPROTEIN)
    Universitas Udayana, 2015
    Co-Authors: Ana Shofi Ani, Retno Iswarin Pujaningsih
    Abstract:

    The objective of this experiment was to examine protection of protein using tannins and saponins toimprove Rumen digestibility and microb-mediated protein synthesis in vitro. Rumen Fluids used as inoculumwas collected from a composite of two female adult fistulatedongole cattle weighed of ±300 kg with theage of five years old. The experimental design used in this study was a completely randomized design withsix treatments and three replication of each treatment. The six treatments consisted of T0: Proteinconcentrates without protection, T1: protein concentrates protected with 1.2% saponin, T2: proteinconcentrates protected with 0.5% tannin and 0.9% saponin , T3: protein concentrates protected with 1.0%tannin and 0.6% saponin, T4: protein concentrates protected with 1.5 % tannin and 0.3% saponin and T5:protein concentrates protected with 2.0% tannins. The result showed that treatment with tannin, saponinand their combination had a significantly affect (P<0,05) on the level of ammonia (NH3), the total volatilefatty acids (VFA), and total protein. Protection of proteins with combination of 1,0% tannin and 0.6%saponin resulted in best effect on feed protein as shown by its NH3 concentration, total VFA and totalprotein. This indicates the level of protection of feed protein can improve Rumen digestibility and microbesmediatedprotein synthesis, as showed in the concentration of N-NH3, total VFA and total protein

L S Jiang - One of the best experts on this subject based on the ideXlab platform.

  • effect of urea fertilization on biomass yield chemical composition in vitro Rumen digestibility and fermentation characteristics of forage oat straw in tibet of china
    The Journal of Agricultural Science, 2016
    Co-Authors: J H Cui, H J Yang, S Bai, S S Song, Wei Sun, X M Shao, L S Jiang
    Abstract:

    The present study investigated the effects of different levels of urea nitrogen (N) fertilizer on nutrient accumulation, in vitro Rumen gas production and fermentation characteristics of forage oat straw (FOS) from oats ( Avena sativa L. ‘Qinghai 444’) grown in the Tibet region of China. Fertilizer, applied at seeding (day 1), stem elongation (days 52–54) and heading (days 63–67), increased plant height and prolonged the maturity stage of the plant by 4–11 days compared with the non-fertilized control. Oat plants were harvested at maturity at the node 3–4 cm above ground, and then separated into grains and FOS. Both FOS and grain yields increased quadratically with increasing N fertilization, and their theoretical maximums occurred at the N fertilizing rates of 439 and 385 kg/ha, respectively. Increases in N fertilization did not affect the hemicellulose content of FOS, but substantially promoted the accumulation of crude protein, cellulose and lignin, resulting in a decrease in the energy content available for metabolism. A 72-h incubation of FOS with Rumen Fluids from lactating cows showed that increasing N resulted in FOS that showed a slower fermentation rate, decreased in vitro dry matter disappearance and lower cumulative gas production, but unchanged fermentation gas composition. Nitrogen fertilization increased the final pH in culture Fluids and decreased the microbial volatile fatty acid (VFA) production. The molar proportions of acetate and propionate were not affected, but molar propionate proportion decreased linearly with increasing urea fertilization, and consequently, the ratio of lipogenic (e.g., acetate and butyrate)-to-glucogenic acids (propionate) tended to increase. In brief, increasing urea N fertilization promoted the growth of forage oats and increased the biomass yield as well as the crude protein and cellulose content of FOS. Considering the negative effect of increased lignin content on nutrient digestibility and total VFA production, the suggested range of urea N fertilization is 156–363 kg N/ha for forage oats planted in Tibet to retain the nutritive value of FOS in the Rumen.

Evelyne Forano - One of the best experts on this subject based on the ideXlab platform.

  • DataSheet1.XLSX
    2018
    Co-Authors: Audrey Segura, Pauline Auffret, Delphine Bibbal, Marine Bertoni, Alexandra Durand, Grégory Jubelin, Monique Kérourédan, Hubert Brugère, Yolande Bertin, Evelyne Forano
    Abstract:

    Healthy cattle are the primary reservoir for O157:H7 Shiga toxin-producing E. coli responsible for human food-borne infections. Because farm environment acts as a source of cattle contamination, it is important to better understand the factors controlling the persistence of E. coli O157:H7 outside the bovine gut. The E. coli O157:H7 strain MC2, identified as a persistent strain in French farms, possessed the characteristics required to cause human infections and genetic markers associated with clinical O157:H7 isolates. Therefore, the capacity of E. coli MC2 to survive during its transit through the bovine gastro-intestinal tract (GIT) and to respond to stresses potentially encountered in extra-intestinal environments was analyzed. E. coli MC2 survived in Rumen Fluids, grew in the content of posterior digestive compartments and survived in bovine feces at 15°C predicting a successful transit of the bacteria along the bovine GIT and its persistence outside the bovine intestine. E. coli MC2 possessed the genetic information encoding 14 adherence systems including adhesins with properties related to colonization of the bovine intestine (F9 fimbriae, EhaA and EspP autotransporters, HCP pilus, FdeC adhesin) reflecting the capacity of the bacteria to colonize different segments of the bovine GIT. E. coli MC2 was also a strong biofilm producer when incubated in fecal samples at low temperature and had a greater ability to form biofilms than the bovine commensal E. coli strain BG1. Furthermore, in contrast to BG1, E. coli MC2 responded to temperature stresses by inducing the genes cspA and htrA during its survival in bovine feces at 15°C. E. coli MC2 also activated genes that are part of the GhoT/GhoS, HicA/HicB and EcnB/EcnA toxin/antitoxin systems involved in the response of E. coli to nutrient starvation and chemical stresses. In summary, the large number of colonization factors known to bind to intestinal epithelium and to biotic or abiotic surfaces, the capacity to produce biofilms and to activate stress fitness genes in bovine feces could explain the persistence of E. coli MC2 in the farm environment.

  • Factors Involved in the Persistence of a Shiga Toxin-Producing Escherichia coli O157:H7 Strain in Bovine Feces and Gastro-Intestinal Content
    Frontiers Media S.A., 2018
    Co-Authors: Audrey Segura, Pauline Auffret, Delphine Bibbal, Marine Bertoni, Alexandra Durand, Grégory Jubelin, Monique Kérourédan, Hubert Brugère, Yolande Bertin, Evelyne Forano
    Abstract:

    Healthy cattle are the primary reservoir for O157:H7 Shiga toxin-producing E. coli responsible for human food-borne infections. Because farm environment acts as a source of cattle contamination, it is important to better understand the factors controlling the persistence of E. coli O157:H7 outside the bovine gut. The E. coli O157:H7 strain MC2, identified as a persistent strain in French farms, possessed the characteristics required to cause human infections and genetic markers associated with clinical O157:H7 isolates. Therefore, the capacity of E. coli MC2 to survive during its transit through the bovine gastro-intestinal tract (GIT) and to respond to stresses potentially encountered in extra-intestinal environments was analyzed. E. coli MC2 survived in Rumen Fluids, grew in the content of posterior digestive compartments and survived in bovine feces at 15°C predicting a successful transit of the bacteria along the bovine GIT and its persistence outside the bovine intestine. E. coli MC2 possessed the genetic information encoding 14 adherence systems including adhesins with properties related to colonization of the bovine intestine (F9 fimbriae, EhaA and EspP autotransporters, HCP pilus, FdeC adhesin) reflecting the capacity of the bacteria to colonize different segments of the bovine GIT. E. coli MC2 was also a strong biofilm producer when incubated in fecal samples at low temperature and had a greater ability to form biofilms than the bovine commensal E. coli strain BG1. Furthermore, in contrast to BG1, E. coli MC2 responded to temperature stresses by inducing the genes cspA and htrA during its survival in bovine feces at 15°C. E. coli MC2 also activated genes that are part of the GhoT/GhoS, HicA/HicB and EcnB/EcnA toxin/antitoxin systems involved in the response of E. coli to nutrient starvation and chemical stresses. In summary, the large number of colonization factors known to bind to intestinal epithelium and to biotic or abiotic surfaces, the capacity to produce biofilms and to activate stress fitness genes in bovine feces could explain the persistence of E. coli MC2 in the farm environment

  • Table1.DOCX
    2018
    Co-Authors: Audrey Segura, Pauline Auffret, Delphine Bibbal, Marine Bertoni, Alexandra Durand, Grégory Jubelin, Monique Kérourédan, Hubert Brugère, Yolande Bertin, Evelyne Forano
    Abstract:

    Healthy cattle are the primary reservoir for O157:H7 Shiga toxin-producing E. coli responsible for human food-borne infections. Because farm environment acts as a source of cattle contamination, it is important to better understand the factors controlling the persistence of E. coli O157:H7 outside the bovine gut. The E. coli O157:H7 strain MC2, identified as a persistent strain in French farms, possessed the characteristics required to cause human infections and genetic markers associated with clinical O157:H7 isolates. Therefore, the capacity of E. coli MC2 to survive during its transit through the bovine gastro-intestinal tract (GIT) and to respond to stresses potentially encountered in extra-intestinal environments was analyzed. E. coli MC2 survived in Rumen Fluids, grew in the content of posterior digestive compartments and survived in bovine feces at 15°C predicting a successful transit of the bacteria along the bovine GIT and its persistence outside the bovine intestine. E. coli MC2 possessed the genetic information encoding 14 adherence systems including adhesins with properties related to colonization of the bovine intestine (F9 fimbriae, EhaA and EspP autotransporters, HCP pilus, FdeC adhesin) reflecting the capacity of the bacteria to colonize different segments of the bovine GIT. E. coli MC2 was also a strong biofilm producer when incubated in fecal samples at low temperature and had a greater ability to form biofilms than the bovine commensal E. coli strain BG1. Furthermore, in contrast to BG1, E. coli MC2 responded to temperature stresses by inducing the genes cspA and htrA during its survival in bovine feces at 15°C. E. coli MC2 also activated genes that are part of the GhoT/GhoS, HicA/HicB and EcnB/EcnA toxin/antitoxin systems involved in the response of E. coli to nutrient starvation and chemical stresses. In summary, the large number of colonization factors known to bind to intestinal epithelium and to biotic or abiotic surfaces, the capacity to produce biofilms and to activate stress fitness genes in bovine feces could explain the persistence of E. coli MC2 in the farm environment.

  • Factors involved in the persistence of a shiga toxin-producing escherichia coil O157:H7 strain in bovine feces and gastro-intestinal content
    Frontiers in Microbiology, 2018
    Co-Authors: Audrey Segura, Pauline Auffret, Delphine Bibbal, Marine Bertoni, Alexandra Durand, Grégory Jubelin, Monique Kérourédan, Hubert Brugère, Yolande Bertin, Evelyne Forano
    Abstract:

    Healthy cattle are the primary reservoir for O157:H7 Shiga toxin-producing E coil responsible for human food-borne infections. Because farm environment acts as a source of cattle contamination, it is important to better understand the factors controlling the persistence of E. coil O157:H7 outside the bovine gut. The E. coil O157:H7 strain MC2, identified as a persistent strain in French farms, possessed the characteristics required to cause human infections and genetic markers associated with clinical O157:H7 isolates. Therefore, the capacity of E. coil MC2 to survive during its transit through the bovine gastro-intestinal tract (GIT) and to respond to stresses potentially encountered in extra intestinal environments was analyzed. E. coil MC2 survived in Rumen Fluids, grew in the content of posterior digestive compartments and survived in bovine feces at 151 degrees C predicting a successful transit of the bacteria along the bovine GIT and its persistence outside the bovine intestine. E coli MC2 possessed the genetic information encoding 14 adherence systems including adhesins with properties related to colonization of the bovine intestine (F9 fimbriae, EhaA and EspP autotransporters, HOP pilus, FdeC adhesin) reflecting the capacity of the bacteria to colonize different segments of the bovine GIT. E coil MC2 was also a strong biofilm producer when incubated in fecal samples at low temperature and had a greater ability to form biofilms than the bovine commensal E. coil strain BG1. Furthermore, in contrast to BG1, E. coli MC2 responded to temperature stresses by inducing the genes cspA and htrA during its survival in bovine feces at 15 degrees C. E coil MC2 also activated genes that are part of the GhoT/GhoS, HicA/HicB and EcnB/EcnA toxin/antitoxin systems involved in the response of E. coil to nutrient starvation and chemical stresses. In summary, the large number of colonization factors known to bind to intestinal epithelium and to biotic or abiotic surfaces, the capacity to produce biofilms and to activate stress fitness genes in bovine feces could explain the persistence of E. coil MC2 in the farm environment.

J H Cui - One of the best experts on this subject based on the ideXlab platform.

  • effect of urea fertilization on biomass yield chemical composition in vitro Rumen digestibility and fermentation characteristics of forage oat straw in tibet of china
    The Journal of Agricultural Science, 2016
    Co-Authors: J H Cui, H J Yang, S Bai, S S Song, Wei Sun, X M Shao, L S Jiang
    Abstract:

    The present study investigated the effects of different levels of urea nitrogen (N) fertilizer on nutrient accumulation, in vitro Rumen gas production and fermentation characteristics of forage oat straw (FOS) from oats ( Avena sativa L. ‘Qinghai 444’) grown in the Tibet region of China. Fertilizer, applied at seeding (day 1), stem elongation (days 52–54) and heading (days 63–67), increased plant height and prolonged the maturity stage of the plant by 4–11 days compared with the non-fertilized control. Oat plants were harvested at maturity at the node 3–4 cm above ground, and then separated into grains and FOS. Both FOS and grain yields increased quadratically with increasing N fertilization, and their theoretical maximums occurred at the N fertilizing rates of 439 and 385 kg/ha, respectively. Increases in N fertilization did not affect the hemicellulose content of FOS, but substantially promoted the accumulation of crude protein, cellulose and lignin, resulting in a decrease in the energy content available for metabolism. A 72-h incubation of FOS with Rumen Fluids from lactating cows showed that increasing N resulted in FOS that showed a slower fermentation rate, decreased in vitro dry matter disappearance and lower cumulative gas production, but unchanged fermentation gas composition. Nitrogen fertilization increased the final pH in culture Fluids and decreased the microbial volatile fatty acid (VFA) production. The molar proportions of acetate and propionate were not affected, but molar propionate proportion decreased linearly with increasing urea fertilization, and consequently, the ratio of lipogenic (e.g., acetate and butyrate)-to-glucogenic acids (propionate) tended to increase. In brief, increasing urea N fertilization promoted the growth of forage oats and increased the biomass yield as well as the crude protein and cellulose content of FOS. Considering the negative effect of increased lignin content on nutrient digestibility and total VFA production, the suggested range of urea N fertilization is 156–363 kg N/ha for forage oats planted in Tibet to retain the nutritive value of FOS in the Rumen.