CN114223793B - 提高母猪繁殖性能的组合物及饲料 - Google Patents
提高母猪繁殖性能的组合物及饲料 Download PDFInfo
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- CN114223793B CN114223793B CN202111284574.2A CN202111284574A CN114223793B CN 114223793 B CN114223793 B CN 114223793B CN 202111284574 A CN202111284574 A CN 202111284574A CN 114223793 B CN114223793 B CN 114223793B
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Abstract
本发明涉及动物养殖领域,特别涉及提高母猪繁殖性能的组合物及饲料。本发明提供了提高母猪繁殖性能的饲喂组合物,包括两种日粮,其一为发情期日粮,包括甜菜粕、L赖氨酸盐酸盐、L‑苏氨酸、缬氨酸、DL‑蛋氨酸、L‑色氨酸、丁酸钠、辛酸、月桂酸。其二为妊娠早期日粮,其特征在于包括甜菜粕、L赖氨酸盐酸盐、L‑苏氨酸、缬氨酸、DL‑蛋氨酸、丁酸钠、辛酸、月桂酸。本发明配制发情期日粮并添加中短链脂肪酸组合、配制妊娠早期低蛋白质日粮,主要调整赖氨酸、苏氨酸、缬氨酸、蛋氨酸的比例和数量,并添加中短链脂肪酸组合,能提高母猪妊娠早期血液中雌激素的水平,能提高母猪窝产活仔数,降低直肠中有害菌的丰度,保障阴道菌群平衡的能力。
Description
技术领域
本发明涉及动物养殖领域,特别涉及提高母猪繁殖性能的组合物及饲料。
背景技术
母猪繁殖性能是影响养猪业生产效率的重要因素,提高母猪的繁殖性能一直是国内外猪营养研究的核心内容之一。猪的胚胎死亡率在所有家畜中是最高的,约为30%-50%。母猪妊娠早期(妊娠的前25天)尤其是胚胎附植期(妊娠13-25天),是早期胚胎存活的敏感时期,死亡率最高可达整个妊娠期胚胎或胎儿死亡率的75%。平衡、精准的营养供应模式和健康的肠道、生殖道微生物环境能有效的改善母胎的健康水平,提高胚胎早期的存活率。因此关注母猪早期胚胎发育的营养水平和母胎生理环境的优劣是降低母猪早期胚胎损失的重要手段。已有研究证实,低蛋白质日粮配制技术能提高母体对日粮氨基酸的利用效率,而中短链脂肪酸则在改善母猪肠道、生殖道健康和提高妊娠早期繁殖性能上均具有显著作用。
目前母猪养殖业中尚无系统针对母猪妊娠早期胚胎损失率高的母猪发情期和妊娠早期营养配方,且无联合添加使用多种中短链脂肪酸组合的营养模式。因此,提供一种提高母猪繁殖性能的饲喂组合物具有重要的生产实践意义。
发明内容
针对母猪妊娠早期胚胎损失率较高,母体肠道、生殖道菌群平衡等问题,本技术发明了母猪发情期和妊娠早期低蛋白质日粮配方,并配合添加功能性理想中短链脂肪酸组合。通过改善母猪发情期及妊娠早期营养水平,添加功能性短中链脂肪酸组合达到提高母猪的繁殖性能的目的。
为了实现上述发明目的,本发明提供以下技术方案:
第一方面,本发明提供了中短链脂肪酸组合,包括如下组分:
丁酸钠 0.1~0.12重量份
辛酸 0.05~0.06重量份
月桂酸 0.1~0.12重量份。
在本发明的一些具体方案中,所述的中短链脂肪酸组合包括如下组分:
丁酸钠 0.1重量份
辛酸 0.05重量份
月桂酸 0.1重量份。
第二方面,本发明还提供了所述的中短链脂肪酸组合在制备母猪发情期和/或母猪妊娠期早期日粮中添加剂中的应用。
第三方面,本发明还提供了所述的中短链脂肪酸组合在制备母猪发情期和/或母猪妊娠期早期日粮中的应用。
第四方面,本发明还提供了母猪发情期和/或母猪妊娠期早期日粮中的添加剂,包括所述的中短链脂肪酸组合以及可接受的辅料。
第五方面,本发明还提供了所述的添加剂在制备母猪发情期和/或母猪妊娠期早期日粮中的应用。
第六方面,本发明还提供了母猪发情期和/或母猪妊娠期早期的日粮,包括所述的中短链脂肪酸组合或所述的添加剂,以及基础日粮;
所述的中短链脂肪酸组合或所述的添加剂中各组分占所述日粮的重量百分含量为:
丁酸钠 0.1%~0.12%
辛酸 0.05%~0.06%
月桂酸 0.1%~0.12%。
在本发明的一些具体实施方案中,所述的中短链脂肪酸组合或所述的添加剂中各组分占所述日粮的重量百分含量为:
丁酸钠 0.1%
辛酸 0.05%
月桂酸 0.1%。
在本发明的一些具体实施方案中,母猪妊娠期早期日粮中,粗蛋白质的重量百分含量为12.49%~12.51%;和/或
母猪发情期日粮中,粗纤维的重量百分含量为:3.49%~3.51%;和/或
母猪妊娠期早期日粮中,粗纤维的重量百分含量为:4.77%~4.79%;和/或
母猪发情期日粮中,L-赖氨酸盐酸盐的重量百分含量为:0.29%~0.30%;和/或
母猪妊娠期早期日粮中,L-赖氨酸盐酸盐的重量百分含量为:0.27%~0.28%;和/或
母猪发情期日粮中,L-苏氨酸的重量百分含量为:0.11%~0.12%;和/或
母猪妊娠期早期日粮中,L-苏氨酸的重量百分含量为:0.09%-0.10%;和/或
母猪发情期日粮中,L-缬氨酸的重量百分含量为:0.09%~0.10%;和/或
母猪妊娠期早期日粮中,L-缬氨酸的重量百分含量为:0.02%~0.03%;和/或
母猪发情期日粮中,DL-蛋氨酸的重量百分含量为:0.05%~0.06%;和/或
母猪妊娠期早期日粮中,DL-蛋氨酸的重量百分含量为:0.02%~0.03%;和/或
母猪发情期日粮中,L-色氨酸的重量百分含量为:0.02%~0.03%;和/或
母猪发情期日粮中,甜菜粕的重量百分含量为:6.3%~6.4%;和/或
母猪妊娠期早期日粮中,甜菜粕的重量百分含量为:8.0%~8.1%。
在本发明的一些具体实施方案中,所述基础日粮包括如下组分:
日粮组成(%,饲喂基础)
1每公斤日粮提供以下营养成分:锌,60mg;铁,95mg;铜,10mg;碘,0.35mg;硒,0.3mg;锰,80mg;维生素A,12,000IU;维生素D3,2,750IU;维生素E,30IU;维生素K3,2mg;维生素B12,12μg;维生素B2,6mg;尼克酸,40mg;泛酸,12mg;维生素B6,3mg;生物素,0.2mg。
本发明提供了提高母猪繁殖性能的饲喂组合物,包括两种日粮,其一发情期日粮,包括甜菜粕、L赖氨酸盐酸盐、L-苏氨酸、缬氨酸、DL-蛋氨酸、L-色氨酸、丁酸钠、辛酸、月桂酸。其二为妊娠早期低蛋白质日粮,其特征在于包括甜菜粕、L赖氨酸盐酸盐、L-苏氨酸、缬氨酸、DL-蛋氨酸、丁酸钠、辛酸、月桂酸。本发明配制发情期日粮并添加中短链脂肪酸组合、配制妊娠早期低蛋白质日粮,主要调整赖氨酸、苏氨酸、缬氨酸、蛋氨酸的比例和数量,并添加中短链脂肪酸组合,能提高母猪妊娠早期血液中雌激素的水平,能提高母猪窝产活仔数,降低直肠中有害菌的丰度,保障阴道菌群健康平衡的能力。
附图说明
为了更清楚地说明本发明实施例或现有技术中的技术方案,下面将对实施例或现有技术描述中所需要使用的附图作简单地介绍。
图1示妊娠14d、28d母猪直肠中微生物门水平组成;注:Con14:对照组妊娠14d样品;Con28:对照组妊娠28d样品;treat14:处理组妊娠14d样品;treat28:处理组妊娠14d样品,下同;
图2示妊娠14d、28d母猪直肠中微生物属水平组成;
图3示妊娠14d、28d母猪直肠微生物组间分布;
图4示妊娠14d、28d母猪直肠中微生物α多样性指数;
图5示妊娠14d、28d母猪直肠微生物主成分分析;
图6示妊娠14d、28d母猪直肠中微生物β多样性指数;
图7示妊娠14d母猪直肠中差异微生物;
图8示妊娠28d母猪直肠中差异微生物;
图9示妊娠14d、28d母猪阴道中微生物门水平组成;
图10示妊娠14d、28d母猪阴道中微生物属水平组成;
图11示妊娠14d、28d母猪阴道微生物组间分布;
图12示妊娠14d、28d母猪阴道中微生物α多样性指数;
图13示妊娠14d、28d母猪阴道微生物主成分分析;
图14示妊娠14d、28d母猪阴道中微生物β多样性指数;
图15示妊娠14d母猪阴道中差异微生物组成;
图16示妊娠28d母猪阴道中差异微生物组成。
具体实施方式
本发明公开了提高母猪繁殖性能的组合物及饲料,本领域技术人员可以借鉴本文内容,适当改进工艺参数实现。特别需要指出的是,所有类似的替换和改动对本领域技术人员来说是显而易见的,它们都被视为包括在本发明。本发明的方法及应用已经通过较佳实施例进行了描述,相关人员明显能在不脱离本发明内容、精神和范围内对本文所述的方法和应用进行改动或适当变更与组合,来实现和应用本发明技术。
本发明提供的提高母猪繁殖性能的组合物及饲料中,所用原料及试剂均可有市场购得。
下面结合实施例,进一步阐述本发明:
实施例1试验设计与日粮
试验选取60头刚结束哺乳期的长×大二元经产母猪(长白猪和大白猪杂交而得到的母猪),按照体重、胎次和背膘随机分为2个处理组(详细信息见表2),每个处理30头母猪。对照组母猪发情期及妊娠早期饲喂日粮根据表1日粮配方配制,试验组母猪发情期及妊娠早期日粮以表1为基础日粮,并额外添加0.1%丁酸钠钠、0.05%辛酸、0.1%月桂酸。
表1日粮组成(%,饲喂基础)
注:1每公斤日粮提供以下营养成分:锌,60mg;铁,95mg;铜,10mg;碘,0.35mg;硒,0.3mg;锰,80mg;维生素A,12,000IU;维生素D3,2,750IU;维生素E,30IU;维生素K3,2mg;维生素B12,12μg;维生素B2,6mg;尼克酸,40mg;泛酸,12mg;维生素B6,3mg;生物素,0.2mg。
实施例2饲养管理
试验在中国农业大学河北丰宁动物试验基地进行。待母猪断奶后,在发情期集中于配种舍进行饲喂,为期6-7天,每头母猪单栏饲养,每天饲喂两次(早上6:00,下午15.30),配种前,每次1.5kg日粮,配种后进行限饲,每次饲喂1.25kg日粮,自由饮水。配种为期2天,采用静立试情,人工授精精的方法,在确认发情后的第一天上午、下午,第二天上午各人工授精1次。配种完成后,母猪集中转移至妊娠舍饲养,每头母猪单栏饲养,每天饲喂两次(早上6:00,下午15.30),每次饲喂1.25kg,自由饮水。在妊娠舍饲养28天,妊娠中期之后所有处理组统一采用试验基地同一种母猪普通妊娠日粮饲喂至分娩。
实施例3样品采集
3.1血液样品
每个处理随机选取5头母猪,于妊娠28d当天清晨空腹采集前腔静脉血5mL,放入不含抗凝剂的采血管中,室温静置1小时后3500r/min离心10分钟,收集血清后于-20℃保存,待测。
3.2直肠微生物
每个处理的所有母猪妊娠14d、28d上午,用15cm无菌棉签从母猪肛门处擦拭直肠部位微生物,随即将棉签头部折断于1.5mL冻存管内,并立即于液氮中快速冷冻,之后冻存于-80℃,待测。
3.3阴道微生物
每个处理的所有母猪14d、28d上午,用15cm无菌棉签从母猪阴道处擦拭直肠部位微生物,随即将棉签头部折断于1.5mL冻存管内,并立即于液氮中快速冷冻,之后冻存于-80℃,待测。
实施例4指标测定与方法
4.1母猪繁殖性能记录
4.1.1母猪体重及背膘的测定
分别于母猪配种、妊娠0d、妊娠28d当天清晨空腹称重,采用超声波背膘仪测量母猪P2点背膘厚度。
4.1.2母猪产仔性能的测定和计算
母猪分娩24h内记录每头母猪产仔数、产活仔数、死胎数、弱仔数(体重小于0.4kg以下)、木乃伊数、总活仔窝重。其中:
总产仔数=产活仔猪数+死胎数+木乃伊数+畸形数
4.2母猪血清激素及胆固醇测定
母猪血清中雌二醇、孕酮及胆固醇的激素含量由北方生物技术有限公司测定。
4.3母猪直肠微生物多样性测定
直肠样品DNA提取、16S rRNA基因的扩增与文库构建、基因测序以及之后的序列拆分、去除barcode、引物均由上海美吉生物医药有限公司完成。
后续数据分析大致操作步骤如下:
1.利用qiime2.0软件q2-Vsearch插件中join-pairs方法进行双端数据合并。
2.利用qiime2.0软件中quality-filter方法对序列进行质控。
3.利用qiime2.0软件DADA2插件进行去噪。
4.利用qime2.0软件中feature-table方法生成OUT表(Operation Taxonomic
Units)。
5.利用qiime2.0软件phylogeny插件中align-to-tree-mafft-fasttree程序进行多序列比对、过滤去除高变区、生成有无根树。
6.利用qiime2.0软件feature-classifier插件classify-sklearn程序和"gg-13-8-99-515-806-nb-classifier.qza"分类器对每个OUT进行分类学注释,得到每个样品在界、门、纲、目、科、属等各个分类上的组成。
7.使用qiime2.0软件对每个样本的Alpha多样性(物种组成丰度及均匀度),以及样本间的Beta多样性(不同样本微生物群落间的相似性)进行计算,得到香农指数(Shannonindex)、sobs指数(OUT数目)、菌群相似性距离矩阵等。另一方面,基于Unfrac距离以及Bray-curtis距离矩阵对样品进行主坐标轴分析(PrincipalCoordinates Analysis,PCoA),对样品进行聚类,从而得到不同样品和分组间的群落结构差异。
4.4母猪阴道微生物多样性测定
试验方法同4.3。
实施例5统计分析
试验得到符合正态分布与非正态分布的两种数据类型。对于正态分布的数据,采用SPSS统计软件中的Student’s T-test检验分别对两组数据进行差异显著性分析。统计结果以P<0.05为差异显著,P<0.01为差异极显著,0.05<P<0.1为具有趋势。对于Alpha多样性、Beta多样性以及微生物的相对丰度等数据采用非参数检验的方法,分别使用MannWhitneyU test和Kruskal-Wallis test对两组或多组数据进行统计分析与比较。效应量线型判别分析(Linear discriminant analysis effect size,LEfSe)是一种基于Kruskal-Wallistest非参数检验的线型判别分析(Linear discriminant analysis,LDA)方法,常用来发现高维数据中的生物标记物,可以实现多个分组间的比较,并在分组比较间的内部进行单组比较。本研究用LEfSe分析对造成组间微生物群落差异的标记细菌进行寻找,阈值设定为2.0(LDA=2.0)。R软件(版本3.4.5)中ggpubr和pheatmap程序包用于绘制箱线图和热图来显示差异微生物的变化。Spearman correlation用于检验不同样本中微生物之间的相互关系。
效果例1发情期和妊娠期日粮添加中短链脂肪酸组合对母猪体况的影响
表2显示了不同处理对母猪体况的影响,由表可知母猪发情期及妊娠早期日粮添加中短链脂肪酸组合对母猪体重,妊娠早期背膘厚均无影响(P>0.05)。
表2不同处理对母猪体况的影响
效果例2发情期和妊娠期日粮添加中短链脂肪酸组合对母猪繁殖性能的影响
表3显示了不同处理对母猪繁殖性能的影响,由表可知母猪发情期及妊娠早期日粮添加中短链脂肪酸组合有提高总产仔数的趋势(P=0.078)。相比于对照组,处理组能极显著提高窝产活仔数(P<0.01),此外还具有提高活仔窝重的趋势(P=0.09)。处理对于平均初生重、公母数、弱仔数、死胎数、畸形数、木乃伊数均无影响(P>0.05)。
表3不同处理对母猪繁殖性能的影响
效果例3发情期和妊娠期日粮添加中短链脂肪酸组合对血液类固醇激素及血液代谢产物的影响
表4显示了不同处理对母猪妊娠28天血液中雌、孕激素的影响,由表可知处理组日粮添加中短链脂肪酸组合能显著提高母猪妊娠28d血液中雌二醇的含量(P<0.05),这有利于妊娠早期母胎稳定以及之后的妊娠结局。表5表明不同处理对母猪妊娠28d血液脂质代谢相关的胆固醇类合成无影响(P>0.05)。
表4母猪妊娠28d血液中雌二醇和孕酮的含量
表5母猪妊娠28d血液中总胆固醇、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇的含量
效果例4发情期和妊娠期日粮添加中短链脂肪酸组合对母猪直肠微生物的影响
图1显示了不同处理,不同妊娠日期母猪直肠中微生物门水平组成情况,处理组和对照组均以放线菌门(Acidobacteriota)、拟杆菌门(Bacteroidota)、弯杆菌门(Campilobacterota)、厚壁菌门(Firmicutes)、梭杆菌门(Fusobacteriota)、变形菌门(Proteobacteria)为优势菌群。图2则显示了属水平母猪直肠微生物组成情况,处理组和对照组中厌氧球菌属(Anaerococcus)、大肠杆菌-志贺菌属(Escherichia-Shigella)、卟啉菌属(Porphyromonas)、梭菌属_sensu_stricto(Clostridium_sensu_stricto_1)、普雷沃氏菌(Prevotella)为主要的属水平微生物。图3表明了不同组间物种组成的分布,处理组独有微生物占2.7%,对照组独有微生物占3.5%。图4、5显示了不同处理、不同妊娠日期母猪直肠微生物的α多样性,由图可知,处理组和对照组之间的α多样性不存在差异。图6则表明了处理组和对照组之间微生物的β多样性,同样,日粮的处理不能影响各组间微生物的β多样性,以上结果均表明,日粮添加中短链脂肪酸组合对母猪妊娠早期直肠中微生物的多样性无显著影响。图7、图8和表6、表7为LEfSe秩和检验结果,图7和表8表明了妊娠第14天处理组和对照组中丰度具有显著差异的微生物。对照组母猪直肠中克林斯菌属丰度显著高于处理组;处理组中微球菌属、红球菌属、毛螺旋菌科_NK4A136_group属、伯克氏菌科_Caballeronia_Paraburkholderia属的丰度显著高于对照组。图8和表7表明了妊娠第28天两组间丰度存在显著差异的微生物。对照组中化脓隐秘杆菌属、脱硫弧菌属、魏斯氏菌属、韦荣氏菌属丰度显著高于处理组,而隐秘杆菌属、Candidatus_Saccharimonas属在处理组中丰度显著高于对照组。由上述结果可知,日粮添加中短链脂肪酸组合对母猪直肠微生物多样性无显著的影响,但已知常见致病菌中,相较于对照组,妊娠28天处理组中与肠道致病致病相关菌化脓隐秘杆菌(Trueperella)的丰度显著降低,而有益菌Candidatus_Saccharimonas属(Candidatus_Saccharimonas)的丰度升高。
表6妊娠14d母猪直肠中差异微生物P值表
表7妊娠28d母猪直肠中差异微生物P值表
效果例5发情期和妊娠期日粮添加中短链脂肪酸组合对母猪阴道微生物的影响
图9显示了不同处理,不同妊娠日期母猪阴道中微生物门水平组成情况,处理组和对照组也均以放线菌门(Acidobacteriota)、拟杆菌门(Bacteroidota)、弯杆菌门(Campilobacterota)、厚壁菌门(Firmicutes)、梭杆菌门(Fusobacteriota)、变形菌门(Proteobacteria)为优势菌群。图10则显示了属水平母猪阴道微生物组成情况,处理组和对照组中不动杆菌属(Acinetobacter)、厌氧球菌属(Anaerococcus)、棒状杆菌属(Corynebacterium)、大肠杆菌-志贺菌属(Escherichia-Shigella)、卟啉菌属(Porphyromonas)、肠球菌属(Campylobacter)等为主要的属水平微生物。图11表明了不同组间物种组成的分布,处理组独有微生物占1.3%,对照组独有微生物占3.1%。图12、13显示了不同处理、不同妊娠日期母猪直肠微生物的α多样性,由图可知,处理组和对照组之间的α多样性不存在差异。图14则表明了处理组和对照组之间微生物的β多样性,由图可知妊娠第28天处理组和对照组微生物β多样性存在显著差异(P<0.05)。图15、16和表8、9为LEfSe秩和检验结果,图15和表8表明了妊娠第14天处理组和对照组中丰度具有显著差异的微生物。对照组母猪阴道中罗氏菌属、巨型球菌属、代尔夫特菌属、大肠杆菌志贺菌属、假单胞菌属丰度显著高于处理组;处理组的DNF00809属、肉杆菌属、克里斯滕森菌科_R-7菌属、八叠球菌属、Howardella属、Moryella属、厌氧球菌属、创伤球菌属、韦荣氏菌属、梭杆菌属、TM7α属丰度显著高于对照组。图16和表9表明了妊娠第28天两组间丰度存在显著差异的微生物。对照组中Iamia属、迪茨氏菌属、红球菌属、短杆菌属、微球菌属、普雷沃菌属_NK3B31_group、特吕珀菌属、脱硫弧菌属、梭菌科_sensu_stricto_1属、毛螺旋菌科_XPB1014_group、伯克氏菌属丰度显著高于处理组,而Muri菌属、拟普雷沃菌属、铁杆菌属、稳杆菌属、巨型球菌属、瘤胃球菌__gnavus_group、毛螺旋菌科_NK4A136_group、Negativicoccus属在处理组中丰度显著高于对照组。由以上结果可知,日粮添加中短链脂肪酸组合能促进母猪阴道菌群平衡。相较于对照组,处理组中与阴道致病性相关的菌属如大肠杆菌志贺菌属(Escherichia_Shigella)、假单胞杆菌属(Pseudomonas)、普雷沃菌属_NK4A136_group(Prevotellaceae_NK3B31_group)、梭菌科_sensu_stricto_1属(Clostridium_sensu_stricto_1)等丰度显著降低,而有益于阴道健康的菌属韦荣氏菌属(Veillonella)丰度要高于对照组。因此饲喂日粮添加中短链脂肪酸组合的母猪阴道微生物的菌群中有害菌相对较少,菌群更健康、平衡。
表8妊娠14d母猪阴道中差异微生物P值表
表9妊娠28d母猪阴道中差异微生物P值表
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。
Claims (2)
1.一种提高母猪繁殖性能的日粮,其特征在于,包括中短链脂肪酸组合或含有中短链脂肪酸组合的添加剂,以及基础日粮;
所述中短链脂肪酸组合中各组分占所述日粮的重量百分含量为:
丁酸钠,0.1%~0.12%;辛酸,0.05%~0.06%;月桂酸,0.1%~0.12%;
所述基础日粮包括如下组分:
发情期的所述基础日粮包括如下组分:
玉米,61.94%;大豆粕,15.5%;膨化大豆,5%;甜菜粕,6.3%;鱼粉,3%;葡萄糖,3%;大豆油,1.3%;磷酸氢钙,1.53%;石粉,0.82%;
预混料,0.5%;食盐,0.4%;L-赖氨酸盐酸盐,0.29%;氯化胆碱,0.15%;纯度98.5%的L-苏氨酸,0.11%;缬氨酸,0.09%;DL-蛋氨酸,0.05%;色氨酸,0.02%;
妊娠期的所述基础日粮包括如下组分:
玉米,61.71%;大豆粕,17.5%;小麦麸,8.1%;甜菜粕,8%;大豆油,0.8%;磷酸氢钙,1.31%;石粉,1.18%;
预混料,0.5%;食盐,0.35%;L-赖氨酸盐酸盐,0.27%;纯度为50%的氯化胆碱,0.15%;纯度为98.5%的L-苏氨酸,0.09%;缬氨酸,0.02%;DL-蛋氨酸,0.02%;
每公斤日粮中的预混料提供以下营养成分:锌,60 mg;铁,95 mg;铜,10 mg;碘,0.35mg;硒,0.3 mg;锰,80 mg;维生素A,12,000 IU;维生素D3,2,750 IU;维生素E,30 IU;维生素K3,2 mg;维生素B12,12 μg;维生素B2,6 mg;尼克酸,40 mg;泛酸,12 mg;维生素B6,3 mg;生物素,0.2 mg。
2.如权利要求1所述的日粮,其特征在于,所述中短链脂肪酸组合中各组分占所述日粮的重量百分含量为:
丁酸钠,0.1%;辛酸,0.05%;月桂酸,0.1%。
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