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1.
添加剂对羊草青贮发酵品质和体外消化率的影响   总被引:9,自引:6,他引:3  
研究乳酸菌制剂、纤维素酶和甲酸对羊草(Leymus chinensis)青贮发酵品质和体外消化率的影响。结果表明:添加乳酸菌制剂、纤维素酶、乳酸菌制剂+纤维素酶均显著降低了青贮饲料pH值,提高了乳酸含量(P<0.05);添加甲酸显著降低了青贮料pH值、乳酸和氨态氮含量(P<0.05);添加乳酸菌制剂或甲酸显著提高了干物质体外消化率(P<0.05),乳酸菌制剂与纤维素酶混合添加显著提高了干物质和粗蛋白质体外消化率(P<0.05)。  相似文献   

2.
本试验旨在探究添加外源纤维酶制剂对青贮玉米体外(瘤胃)发酵的影响。试验采用单因素试验设计,利用压力读取式体外产气系统,添加11种纤维酶制剂,包括5种纤维素酶(CEL-1、CEL-2、CEL-3、CEL-4、CEL-5)和6种木聚糖酶(XYL-1、XYL-2、XYL-3、XYL-4、XYL-5、XYL-6),对照组不添加酶制剂,纤维素酶组添加水平为30 U/g,木聚糖酶组添加水平为40 U/g。结果表明:与对照组相比,添加纤维素酶显著降低了底物的潜在产气量(P<0.05),但是显著提高了产气速率(P<0.05),其中添加CEL-1提升产气速率达82.5%;但除XYL-3显著降低了潜在产气量(P<0.05)外,添加木聚糖酶对其他产气参数均无显著影响(P>0.05)。除了XYL-4对酸性洗涤纤维降解率效果不显著(P>0.05)外,酶制剂组的干物质、中性洗涤纤维和酸性洗涤纤维降解率都显著提高(P<0.05)。添加XYL-1、XYL-4和CEL-5显著提高了总挥发性脂肪酸的产量(P<0.05),XYL-3和XYL-4均显著降低了乙酸摩尔比和乙酸∶丙酸(P<0.05),显著提高了丙酸摩尔比(P<0.05),但仅XYL-4显著提高了丁酸摩尔比(P<0.05)。体外培养6和12h时,不同酶制剂对甲烷生成的影响呈现较大的变异性,培养到24 h时,酶制剂对甲烷生成的影响变得不显著(P>0.05)。由此可知,添加外源纤维酶制剂可提高青贮玉米的干物质、中性洗涤纤维和酸性洗涤纤维的降解率,并可在培养前期改变甲烷的生成量。  相似文献   

3.
本试验旨在探究不同酶制剂组合对水稻秸秆青贮品质和体外瘤胃发酵特性的影响。试验以水稻秸秆为青贮原料,添加不同酶制剂组合,共设4个组:对照组(CK组,不添加任何酶制剂)、C组(添加1.0 g/kg纤维素酶、木聚糖酶、β-葡聚糖酶复合酶制剂)、PL组(添加0.5 g/kg果胶酶+1.0 g/kg漆酶)、CPL组(添加1.0 g/kg纤维素酶、木聚糖酶、β-葡聚糖酶复合酶制剂+0.5 g/kg果胶酶+1.0 g/kg漆酶),每组5个重复。青贮60 d后开包取样,分析其青贮品质和体外瘤胃发酵特性。结果表明:1)水稻秸秆青贮后,PL组的干物质含量显著高于CK、C、CPL组(P<0.05);CPL组的粗脂肪含量、相对饲用价值、总可消化养分显著高于CK组(P<0.05),中性洗涤纤维和酸性洗涤纤维含量显著低于CK组(P<0.05)。2)体外发酵24 h后,C、PL、CPL组24 h累积产气量、慢速降解部分产气量和潜在产气量显著高于CK组(P<0.05),快速部分产气量显著低于CK组(P<0.05);PL、CPL组的慢速降解部分的产气速率显著高于CK、C组(P<0.0...  相似文献   

4.
为探讨延胡索酸二钠对瘤胃甲烷产量及瘤胃微生物发酵活力的影响,本研究共设计了3个试验来阐明该问题。试验1采用体外批次培养,研究了不同日粮条件下(高牧草日粮、中等水平牧草的日粮和低牧草日粮)添加延胡索酸二钠(0,4和7mmol/L)对山羊瘤胃微生物发酵及甲烷产量的影响。结果表明,较对照相比,添加延胡索酸二钠显著提高了累积产气量、pH值和TVFA产量(P<0.05),降低了甲烷产量(P<0.05),其中高牧草日粮组下降幅度最大。试验2探讨了延胡索酸二钠对黄化瘤胃球菌发酵粗饲料活力的影响。结果表明,与对照组相比;添加延胡索酸二钠显著提高了黄化瘤胃球菌数量及其对黑麦草的降解率(P<0.05);试验3探讨了延胡索酸二钠对瘤胃真菌发酵粗饲料活力的影响,结果显示,延胡索酸二钠显著降低了厌氧真菌发酵的总产气量、干物质消失率及羧甲基纤维素酶酶活(P<0.05)。结果说明,延胡索酸二钠在降低甲烷产量方面与发酵底物的天然特性有关,其中对高牧草日粮的作用效应最为显著;延胡索酸二钠可提高瘤胃混合微生物与瘤胃纤维降解菌发酵粗饲料的能力,但对瘤胃真菌的发酵活力具有抑制效应。  相似文献   

5.
本研究旨在探讨添加不同酶制剂对全株玉米青贮发酵品质的影响,以蜡熟期刈割的全株玉米为材料,设对照组和6个处理组,处理组分别添加5 g/kg纤维素酶、木聚糖酶、果胶酶、α-半乳糖苷酶、β-甘露聚糖酶和β-葡聚糖酶,每组3个重复,青贮56 d后对全株玉米青贮饲料的感官评定、发酵品质、营养成分进行比较分析。结果显示:纤维素酶组、木聚糖酶组和β-葡聚糖酶组全株玉米青贮饲料的青贮效果较好;与对照组相比,纤维素酶组、木聚糖酶组和β-葡聚糖酶组可显著提高青贮饲料碳水化合物(WSC)和乳酸的含量(P>0.05),同时使青贮氨态氮/总氮显著降低(P<0.05),青贮发酵品质较好;添加纤维素酶的全株玉米青贮中干物质(DM)含量高于对照组和其他处理组,添加纤维素酶和α-半乳糖苷酶处理的粗蛋白质(CP)含量较高;添加纤维素酶的酸性洗涤纤维(ADF)和β-葡聚糖酶组青贮中性洗涤纤维(NDF)、ADF均显著低于对照组(P<0.05)。综上表明:纤维素酶、木聚糖酶和β-葡聚糖酶更适于用作全株玉米青贮饲料的添加剂。  相似文献   

6.
本研究旨在探讨添加不同酶制剂对全株玉米青贮发酵品质的影响,以蜡熟期刈割的全株玉米为材料,设对照组和6个处理组,处理组分别添加5 g/kg纤维素酶、木聚糖酶、果胶酶、α-半乳糖苷酶、β-甘露聚糖酶和β-葡聚糖酶,每组3个重复,青贮56 d后对全株玉米青贮饲料的感官评定、发酵品质、营养成分进行比较分析。结果显示:纤维素酶组、木聚糖酶组和β-葡聚糖酶组全株玉米青贮饲料的青贮效果较好;与对照组相比,纤维素酶组、木聚糖酶组和β-葡聚糖酶组可显著提高青贮饲料碳水化合物(WSC)和乳酸的含量(P0.05),同时使青贮氨态氮/总氮显著降低(P0.05),青贮发酵品质较好;添加纤维素酶的全株玉米青贮中干物质(DM)含量高于对照组和其他处理组,添加纤维素酶和α-半乳糖苷酶处理的粗蛋白质(CP)含量较高;添加纤维素酶的酸性洗涤纤维(ADF)和β-葡聚糖酶组青贮中性洗涤纤维(NDF)、ADF均显著低于对照组(P0.05)。综上表明:纤维素酶、木聚糖酶和β-葡聚糖酶更适于用作全株玉米青贮饲料的添加剂。  相似文献   

7.
为探讨纤维素酶和木聚糖酶对象草(Pennisetum purpureum Schumach)青贮发酵品质与体外消化率的影响,试验设对照组(CK)、添加纤维素酶组(CE)、添加木聚糖酶组(XE)和组合添加酶组(CX,纤维素酶+木聚糖酶)。青贮7,30,60,90 d后开窖取样,测定相关指标。结果表明:与对照组相比,CE,XE和CX组显著提高了乳酸含量(P<0.05),降低了pH、氨态氮/总氮和干物质损失;添加酶处理组中性洗涤纤维(Neutral detergent fiber,NDF)、酸性洗涤纤维(Acid detergent fiber,ADF)、纤维素、半纤维素含量均低于对照,并且水溶性碳水化合物、葡萄糖、果糖和蔗糖含量增加;体外发酵试验中,CE,XE和CX组青贮饲料干物质消化率、中性洗涤纤维消化率、酸性洗涤消化率和体外产气均显著高于CK(P<0.05),且CX组体外产气量最高,而CE与XE之间差异不显著。综上,添加纤维素酶、木聚糖酶提高了象草青贮发酵品质与体外消化率,组合添加酶效果更好。  相似文献   

8.
酵母膏不同添加量对瘤胃真菌体外培养的影响   总被引:1,自引:0,他引:1  
通过体外培养,研究酵母膏的不同添加量对瘤胃真菌体外培养的影响。培养底物中分别添加0,5%,15%酵母膏,在39℃恒温培养,分别测定0,24,48,72和96 h 6个培养时间点的羧甲基纤维素酶、木聚糖酶、微晶纤维素酶活性,并分析培养96 h真菌培养底物中的粗蛋白,真蛋白和粗纤维含量。结果表明,酵母膏添加量显著影响纤维素酶活(P<0.05),纤维素酶活在24、48 h时最高,随酵母添加量增大,培养底物的粗蛋白和真蛋白含量也明显增大,粗纤维含量各组差异不显著(P>0.05)。  相似文献   

9.
外源多糖降解酶对纯底物发酵动力学及消失率影响   总被引:1,自引:0,他引:1  
采用活体外产气量法测定外源添加的纤维素酶、木聚糖酶和β-葡聚糖酶对绵羊瘤胃发酵动力学及消失率的影响。以木聚糖和微晶纤维素为底物,选用木聚糖?微晶纤维素和木聚糖与微晶纤维素的等量混合物0.2g,酶添加水平分别为:纤维素酶为0,5000,10000和15000U/mL;木聚糖酶为0,360,3600和36000U/mL;β-葡聚糖酶为0,320,3200,和32000U/mL,每个组设3个重复,来测定3种酶对瘤胃降解微晶纤维素和木聚糖及二者混合物的产气速率、延滞期和最大产气量的影响。试验结果显示,利用体外产气量法测定外源多糖降解酶对以纯微晶纤维素和木聚糖为底物96h的消失率影响不显著(P>0.05),对底物的发酵动力学的影响,不同处理、不同酶及底物之间也不相同,木聚糖酶试验中,2种底物在消失率方面有相互促进作用。  相似文献   

10.
绞股蓝皂甙对体外瘤胃微生物甲烷产量及发酵特性的影响   总被引:1,自引:1,他引:0  
利用体外产气量法研究绞股蓝皂甙对山羊瘤胃微生物体外甲烷产量及发酵特性的影响。试验包括2个部分,试验一研究了绞股蓝皂甙对瘤胃微生物甲烷产量及发酵特性的影响,试验二分析绞股蓝皂甙对瘤胃微生物发酵动力学参数的影响。试验以0.42 g羊草+0.126 g玉米+0.054 g豆粕为发酵底物,60 mL培养基中的绞股蓝皂甙添加量分别为0(对照),5,10,20和40 mg,发酵24 h。与对照组比较,发酵8 h,各处理组甲烷浓度显著下降(P<0.05),分别下降30.20%,43.49%,44.67%和75.8%;12 h,20 mg组显著下降(P<0.05),40 mg组极显著下降(P<0.01),处理组甲烷浓度分别下降6.97%,9.63%,18.90%和61.82%;24 h,10 mg组显著下降(P<0.05),40 mg组极显著下降(P<0.01),处理组甲烷浓度分别下降2.34%,9.39%,6.90%和20.73%,甲烷浓度与皂甙剂量之间有极显著的线性效应(P<0.01)。10 mg组的氢利用率极显著低于对照组,其他试验组无显著变化。10 mg组显著提高了TVFA及乙酸、丙酸、异丁酸、戊酸、异戊酸和支链脂肪酸浓度(P<0.05),40 mg组丁酸的浓度极显著下降(P<0.01)。10 mg组和20 mg组乙丙比显著高于对照组(P<0.05)。随着皂甙剂量增加,乙酸、丁酸、异丁酸、戊酸、异戊酸、支链脂肪酸、总挥发性脂肪酸浓度及乙丙比呈显著或极显著的二次方效应,丁酸同时具有极显著的线性效应。处理组原虫数量显著(P<0.05)或极显著下降(P<0.01)(40 mg组),且与皂甙剂量间存在极显著的线性和二次方效应(P<0.01)。微生物蛋白含量没有显著变化,但呈上升趋势。10 mg组和40 mg组的氨态氮浓度显著升高(P<0.05),氨态氮浓度与皂甙剂量之间有显著的线性效应(P<0.05)。高剂量绞股蓝皂甙降低了微生物发酵的理论与实际产气量,并呈显著的线性和二次方效应,产气速率与皂甙剂量之间有着显著的线性效应。以上结果表明绞股蓝皂甙能改变瘤胃微生物发酵模式,降低瘤胃微生物的甲烷产量,提高VFA的产量,有利于饲料能量的利用,同时缓解甲烷对大气环境的污染。  相似文献   

11.
为探讨纤维素酶、木聚糖酶及两种酶组合添加对水稻秸秆青贮过程中结构性、水溶性碳水化合物组分含量及体外消化特性和发酵品质的影响,试验设4个处理组:1)0.3%蒸馏水(对照组,CO);2)0.3%纤维素酶(CE);3)0.3%木聚糖酶(XE);4)0.15%纤维素酶+0.15%木聚糖酶(组合酶组,CX),分别于青贮3、7、14、30 d后取样分析。结果表明,与CO相比,CE、XE和CX组显著提高了乳酸、葡萄糖、果糖和蔗糖含量,显著降低了pH值、氨态氮、总挥发性脂肪酸、酸性洗涤纤维、中性洗涤纤维、纤维素和半纤维素含量,减少了干物质损失(P<0.05)。酶制剂显著提高了水稻秸秆青贮饲料24、48和72 h时的累积产气量和干物质体外消化率(P<0.05)。青贮末期CX组有最高的乳酸含量(34.13 g·kg-1DM)、体外产气量(68.27 mL)、干物质体外消化率(61.31%)和最低的pH值(4.36)。与CE和XE相比,CX组水溶性碳水化合物(葡萄糖、果糖和蔗糖)含量更高。综上所述,添加酶制剂可促进结构性碳水化合物的降解,提高水溶性碳水化合物的含量,改善水稻...  相似文献   

12.
Two experiments were conducted to evaluate the effect of four enzyme additives on ruminal fermentation of corn silage using a 48 h batch culture in vitro assay with buffer and ruminal fluid. Experiment 1 (Exp. 1) and Experiment 2 (Exp. 2) were conducted as completely randomized designs each with two runs and four replicates. The enzyme additives (E1, E2, E3, and E4) were commercial products that provided a range in endoglucanase, exoglucanase, and xylanase activities. For both xylanase (birch wood and oat spelt substrate) and endoglucanase (carboxymethylcellulose substrate), the enzyme products (per ml) were ranked E4>E1>E2>E3. In Exp. 1, the four enzymes were added at 0, 2, 4, and 8 μl/g of corn silage dry matter (DM), whereas in Exp. 2 enzymes were added at 0, 0.5, 1, 2, and 4 μl/g DM. Gas production (GP) was measured at 3, 6, 12, 18, 24, and 48 h after incubation. Disappearance of DM (DMD), neutral detergent fiber (NDFD), and acid detergent fiber (ADFD), and volatile fatty acid concentrations (VFA; total and individual molar proportions) were determined after 24 and 48 h. In Exp. 1, E1 and E2 had higher NDFD and ADFD at 24 and 48 h of incubation (P<0.001) compared with E3 and E4. Increasing dose rate increased NDFD and ADFD for all enzymes (except ADFD for E4 at 48 h), with the optimum dose rate dependant on the enzyme additive (dose×enzyme; P<0.01). There were some treatment effects on DMD and total GP at 24 and 48 h, but these responses were not consistent with responses in NDFD and ADFD. Experiment 2 was conducted to confirm the effects and optimum dose rate of each enzyme additive. In Exp. 2, DMD was not affected by enzyme after 24 and 48 h incubation. There were no enzyme×dose interactions for DMD, NDFD, or ADFD after 24 or 48 h of incubation (except for ADFD at 48 h). After 24 h, DMD, NDFD, and ADFD increased linearly with increasing dose (P<0.05); after 48 h DMD increased linearly, whereas NDFD increased quadratically with increasing enzyme dose (P<0.05). The ADFD increased linearly after 48 h for E3 and E4, but after 48 h ADFD increased quadratically for E1 and E2. Total GP was consistently lowest for E4 at both incubation times (P<0.05). There were no enzyme×dose interactions (P>0.05) for any of the fermentation variables at either 24 or 48 h of incubation in Exp. 2. There were differences amongst the additives for total VFA at 24 and 48 h (P≤0.05); increasing enzyme dose decreased total VFA after 24 h but increased total VFA at 48 h, such that all doses were higher than the control (P<0.001). Overall, the enzyme additives increased NDFD and ADFD of corn silage in vitro; however, E1 and E2 were more effective than E3 or E4. Responses to increasing dose of enzyme were generally linear or curvilinear, and the optimum dose rate differed amongst the products evaluated. Evaluation of the enzymes at 24 and 48 h generally led to the same ranking of the additives, and the degradation of NDF and ADF was more useful in differentiating the enzymes compared with DM and total GP.  相似文献   

13.
试验旨在利用Box-Behnken响应面法优化蒸汽爆破预处理小麦秸秆最佳条件,从而解决小麦秸秆营养成分利用率较低的问题。选取蒸汽压强(1.5~2.5 MPa)、水分含量(10%~50%)和维压时间(90~210 s)为自变量,瘤胃体外发酵产气速率为响应值,利用响应面建立回归模型并进行回归方程拟合,预测最佳工艺参数。结果显示:维压时间对瘤胃体外发酵产气速率的影响极显著(P<0.01),蒸汽压强和水分含量对瘤胃体外发酵产气速率无显著影响(P>0.05)。由F值可知:3个自变量对瘤胃体外发酵产气速率的影响大小依次为维压时间、蒸汽压强和水分含量。Box-Behnken响应面法优化蒸汽爆破预处理小麦秸秆的最优工艺参数为蒸汽压强1.77 MPa、水分含量49.91%和维压时间209.98 s。此条件下瘤胃体外发酵产气速率可达0.0794 mL/h。3次平行试验验证的体外发酵产气速率为0.0786 mL/h,与理论预测值误差仅为1.02%。将小麦秸秆在最佳爆破条件下重新爆破并进行体外发酵试验,与未蒸汽爆破的小麦秸秆相比,蒸汽爆破极显著降低了小麦秸秆中中性洗涤纤维(NDF)、酸性洗涤纤维(ADF)和半纤维素的含量(P<0.01),同时极显著提高了体外发酵液中挥发性脂肪酸(VFA)和NH3-N的含量(P<0.01)。综上,采用响应面法优化蒸汽爆破小麦秸秆的条件合理可行,优化的蒸汽爆破参数可用于提高小麦秸秆营养价值的蒸汽爆破工艺中。  相似文献   

14.
马大川  武杰  李娟  单春乔 《中国畜牧兽医》2020,47(12):3917-3925
本试验旨在研究复合酶及复合酶菌制剂对奶牛日粮体外降解率及不同阶段奶牛产奶性能的影响。在体外试验中,分别以基础日粮(Ⅰ组)及基础日粮中分别添加复合酶制剂(Ⅱ组)、复合酶菌制剂(Ⅲ组)的日粮作为发酵底物,体外培养72 h,测定不同时间点(6、12、24、36、48、72 h)日粮干物质降解率(DMD)和粗蛋白质降解率(CPD)。在饲养试验中,分别选取体重、胎次、体况相近的泌乳前期(30 d±5 d)、泌乳中期(100 d±5 d)和泌乳后期(250 d±5 d)奶牛各24头,平均分成3组,其中对照组(Ⅰ组)奶牛饲喂全混合日粮(TMR),复合酶制剂组(Ⅱ组)和复合酶菌制剂组(Ⅲ组)奶牛在TMR中分别添加1 kg/t的复合酶制剂和复合酶菌制剂。每期试验持续74 d,其中预试期14 d,正试期60 d,每天记录产奶量。结果显示:①体外试验中,Ⅱ、Ⅲ组的DMD、CPD均随处理时间的延长而增加。在各个时间点,Ⅲ组的DMD、CPD均高于Ⅱ组,其中DMD在6、72 h时差异显著(P<0.05),CPD在36、72 h时差异显著(P<0.05),在其他时间点差异均不显著(P>0.05)。②在泌乳前期,Ⅱ、Ⅲ组的平均日产奶量与Ⅰ组相比分别提高了3.68%和4.10%,差异显著(P<0.05),Ⅱ、Ⅲ组之间差异不显著(P>0.05);泌乳中期,Ⅱ、Ⅲ组的平均日产奶量与Ⅰ组相比分别提高了7.53%和10.66%,差异显著(P<0.05),Ⅱ、Ⅲ组之间差异不显著(P>0.05);泌乳后期,Ⅱ、Ⅲ组的平均日产奶量与Ⅰ组相比分别提高了7.06%和5.16%,差异显著(P<0.05),Ⅱ组、Ⅲ组之间差异不显著(P>0.05)。综上,复合酶与复合酶菌制剂均能在一定程度上提高日粮体外DMD和CPD以及奶牛在不同时期的产奶量,其中,复合酶制剂对提高泌乳后期奶牛产奶量效果更好,复合酶菌制剂对提高泌乳中期奶牛产奶量效果更好。  相似文献   

15.
The purpose of this experiment was to study the effect of compound enzyme and compound enzyme bacteria preparation on the degradation rate of diet in vitro and milk production performance of dairy cows at different lactation stages.In in vitro experiment,the basic diet (group Ⅰ) and the basic diet added with compound enzyme (group Ⅱ) and compound enzyme probiotics preparation (group Ⅲ) were used as fermentation substrate respectively.After 72 h of culture in vitro,the dry matter degradation rate (DMD) and crude protein degradation rate (CPD) of the diet were measured at different time (6,12,24,36,48 and 72 h).In feeding experiment,24 dairy cows with similar body weight,parity and condition were divided into three groups at early lactation (30 d±5 d),middle lactation (100 d±5 d) and late lactation (250 d±5 d),respectively.The cows in control group (group Ⅰ) were fed with TMR,in compound enzyme group (group Ⅱ) and the compound enzyme probiotics group (group Ⅲ) were fed with the TMR added with 1 kg/t compound enzyme and compound enzyme probiotics respectively.The trial period was 74 days,including 14 days of pre trial period and 60 days of normal trial period.`The results showed that:①In vitro DMD and CPD of the two groups increased with the prolongation of treatment time.At each time point,the values of DMD and CPD in group Ⅲ were higher than those in group Ⅱ,the difference of DMD was significant at 6 and 72 h (P<0.05),CPD was significant at 36 and 72 h (P<0.05),and there was no significant difference at other time points (P>0.05).②In the early stage of lactation,the average daily milk production of groups Ⅱ and Ⅲ increased by 3.68% and 4.10% respectively compared with group Ⅰ,the difference was significant (P<0.05),and the difference between groups Ⅱ and Ⅲ was not significant (P>0.05).In mid-lactation,the average daily milk production of groups Ⅱ and Ⅲ increased by 7.53% and 10.66% respectively compared with group Ⅰ (P<0.05),and the difference between groups Ⅱ and Ⅲ was not significant (P>0.05).In the later stage,the average daily milk production of groups Ⅱ and Ⅲ increased by 7.06% and 5.16% respectively compared with group Ⅰ (P<0.05),and the difference between group Ⅱ and Ⅲ was not significant (P>0.05).In conclusion,both compound enzymes and compound enzyme probiotics preparations could improve the in vitro DMD and CPD of the diet and the milk production of dairy cows in different periods to a certain extent.Among them,the compound enzyme preparation had a better effect on increasing milk production of dairy cows in the late lactation,while the compound enzyme probiotics preparation has a better effect on increasing milk production in mid-lactating dairy cows.  相似文献   

16.
本试验以精料、青干草和单宁酸作为发酵底物,研究添加不同水平单宁酸对绵羊体外发酵参数和甲烷产量、干物质和粗蛋白质降解率的影响,以期为体内试验筛选适宜的单宁酸浓度,为富含单宁的粗饲料资源应用于反刍动物日粮配制及减少反刍动物养殖过程种甲烷排放提供科学依据。采用体外批次培养法开展研究,发酵底物为精料、青干草和单宁酸,设置底物的精粗比为3∶7。根据单宁酸添加量分为6组,单宁酸添加量分别为0、0.5%、1.0%、1.5%、2.0%、3.0%,发酵时间设置为3、6、12和24 h,每个处理3个重复,测定各培养时间pH、氨氮(NH3-N)浓度、挥发性脂肪酸(VFA)浓度、总产气量、甲烷产量、干物质和粗蛋白质降解率。结果显示,培养至3 h时,1.0%和2.0%单宁酸添加组pH显著高于对照组(P<0.05),其他时间点各组pH无显著差异(P>0.05);1.0%、2.0%和3.0%单宁酸添加组NH3-N浓度显著低于对照组(P<0.05);培养至6和24 h时,各处理组NH3-N浓度均显著低于对照组(P<0.05)。培养至6 h时,2.0%单宁酸添加组乙酸、丙酸、丁酸和总VFA浓度均显著低于对照组(P<0.05);培养至24 h时,1.0%、1.5%和3.0%单宁酸添加组的丙酸、丁酸和总VFA浓度均显著低于对照组(P<0.05);各单宁酸添加组4个时间点丙酸、丁酸、总VFA浓度的平均值均显著低于对照组(P<0.05)。培养至12、24 h时,各处理组总产气量与对照组差异不显著(P>0.05);培养至12 h时,2.0%组甲烷产量显著低于对照组、0.5%组和1.0%组(P<0.05);培养至24 h时,2.0%和3.0%组的甲烷产量显著低于对照组(P<0.05)。因此,添加单宁酸会显著降低体外发酵的NH3-N浓度,抑制VFA的产量,添加1.5%、2.0%的单宁酸能够显著降低瘤胃发酵甲烷产量,添加单宁酸的处理组粗蛋白质降解率显著低于对照组。  相似文献   

17.
【目的】研究柠檬苦素(limonin,Lim)对小鼠卵母细胞体外成熟(IVM)及后续体外受精(IVF)胚胎发育潜能的影响,旨在为体外成熟培养系统的优化提供参考。【方法】在小鼠体外成熟培养液中添加不同浓度的Lim(0、10、20、50 μmol/L),成熟培养12 h后统计小鼠卵母细胞第一极体(PBI)排出率,筛选体外成熟培养液中添加Lim的最适浓度;在体外成熟培养液中添加最适浓度的Lim,以0 μmol/L Lim为对照组,成熟培养12 h,通过免疫荧光染色检测活性氧(ROS)、谷胱甘肽(GSH)以及线粒体膜电位(MMP)水平;通过实时荧光定量PCR检测卵母细胞抗氧化及凋亡相关基因的mRNA表达水平。将最适Lim组及对照组卵母细胞体外成熟24 h后进行体外受精,于体外受精24 h和3.5 d分别统计胚胎卵裂率和囊胚率,并用Fluorescein-dUTP和Hoechst 33342染色分别检测囊胚总细胞数及囊胚内凋亡细胞比率。【结果】与0 μmol/L Lim组相比,20 μmol/L Lim组小鼠卵母细胞PBI排出率显著升高(P<0.05),后续试验均用20 μmol/L Lim进行处理。与对照组组相比,20 μmol/L Lim组小鼠卵母细胞内ROS水平显著降低(P<0.05),GSH、MMP水平均显著增加(P<0.05),抗氧化相关基因(GPx3、CAT和Prdx3)、抗凋亡相关基因(Bcl-2、Bcl-xl)表达水平均显著上调(P<0.05),促凋亡相关基因(Caspase-3)表达水平显著下调(P<0.05);体外受精胚胎的卵裂率、囊胚率、囊胚总细胞数均显著增加(P<0.05),囊胚内细胞凋亡比率显著下降(P<0.05)。【结论】在体外成熟培养液中添加20 μmol/L Lim可以通过抑制氧化应激和细胞凋亡、增加MMP水平提高小鼠卵母细胞质量,从而提高体外受精胚胎的发育潜力。  相似文献   

18.
The test was aimed at determining the effects of adding MOS to diets with different concentrate to forage ratios on ruminal fermentation of sheep in vitro.The 4×6 two-factor experimental design was chosen.There were 4 diets with different concentrate to forage ratios(20:80, 30:70, 40:60 and 50:50) and added to 6 dosages MOS(0, 0.4%, 0.8%, 1.2%, 1.6% and 2.0%), respectively.The method of gas production in vitro was used to measure the total gas and CH4 production, IVDMD, IVCPD and IVOMD after cultured for 3, 6, 9, 12 and 24 h.The results showed that the gas(except 12 and 24 h) and CH4 production(except 9 h) were not impacted by the two factors(P>0.05).The IVDMD, IVCPD and IVOMD were significantly affected by concentrate to forage ratios(P<0.05), while the IVCPD at 24 h was significantly affected by MOS(P<0.05).Meanwhile, all the indexes were not influenced by the interaction of two factors(P>0.05).The IVDMD and IVOMD increased with the rising of concentrate approximately, while the IVCPD decreased with the rising of MOS roughly.The biggest associative effect was gained in 30:70 concentrate to forage diet when adding 1.2% MOS.  相似文献   

19.
为了探究添加亚油酸条件下不同剂量硝酸钠对水牛瘤胃体外发酵脂肪酸组成及相关微生物数量的影响,本试验选用3头装有永久性瘤胃瘘管的母水牛,以精粗比40∶60为底物进行瘤胃液体外发酵试验。试验组硝酸钠的浓度分别为1、2、3 mg·mL-1,对照组不加硝酸钠,每组均添加0.25 mg·mL-1的亚油酸,每组各5个重复。在体外培养3、6、9、12、24 h时测定产气量和甲烷产量,24 h结束培养,测定瘤胃体外发酵参数、脂肪酸含量及瘤胃微生物数量。结果表明:1)添加硝酸钠显著降低了总产气量和甲烷产量(P<0.05);2)添加硝酸钠pH值和氨态氮(NH3-N)含量显著升高(P<0.05),异丁酸和异戊酸含量显著降低(P<0.05),而对总挥发性脂肪酸(TVFA)含量无显著性影响(P>0.05);3)添加1 mg·mL-1硝酸钠,C18:2cis-9,trans-11、C18:2trans-10,cis-12含量和不饱和脂肪酸/饱和脂肪酸(UFA/SFA)显著高于其他组(P<0.05),且C20:5n3 (EPA)含量显著高于添加3 mg·mL-1硝酸钠组(P<0.05),添加2 mg·mL-1硝酸钠C22:6n3 (DHA)含量显著高于其他组(P<0.05);4)添加硝酸钠组原虫数量显著低于对照组(P<0.05),添加2、3 mg·mL-1硝酸钠产甲烷菌数量显著低于添加1 mg·mL-1硝酸钠组(P<0.05),添加1 mg·mL-1硝酸钠总细菌、真菌、溶纤维丁酸弧菌、蛋白分解丁酸弧菌、非典型丁酸弧菌、亨氏丁酸弧菌数量显著高于其他组(P<0.05)。由此可得,体外法添加1~3 mg·mL-1硝酸钠和0.25 mg·mL-1亚油酸在维持水牛TVFA含量不变的情况下显著降低了甲烷含量,且1 mg·mL-1硝酸钠能促进亚油酸生成共轭亚油酸(CLA),优化脂肪酸组成,并能增加大多数瘤胃微生物的数量。  相似文献   

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