大豆多肽的性质及其研究进展

大豆多肽(Soy peptide)是大豆蛋白质经酶解作用后的多肽分子混合物。与大豆蛋白相比,大豆肽具有更好的理化性质,含有多种生理活性物质,在机体内具有更多种生理功能,近年来引起人们的广泛关注。     

多拉菌素在猪体内的药代动力学

对多拉菌素在猪体内进行为期45d的药代动力学研究。长白×杜洛克杂交猪10头,临床健康,驱净寄生虫,体重36～50kg,以300μg/kg体重剂量分别通过静脉和肌肉注射给药。动物给药后在不同时间内分点经颈静脉采血。血浆样品用乙腈沉淀处理,上清液过C18富集柱,用甲醇提取多拉菌素并进行衍生化反应,以反向HPLC测定猪血清中的药物浓度。药代动力学参数用计算机程序MCPKP进行处理。结果表明,动物经静脉和肌肉注射给药后,血浆药物浓度分别可测至30d和25d,2种途径的药物浓度时间曲线均符合二室开放模型。主要药代动力学参数为:静脉注射T1/2α(1.092±0.66)d,T1/2β(6.11±2.73)d,AUC(274.19±119.89)μg/(L·d);肌肉注射T1/2α(0.056±0.022)d,T1/2β(3.20±1.34)d,AUC(223.51±65.20)μg/(L·d),CMAX(28.99±10.69)μg/L,Tp(1.24±0.87)d。多拉菌素肌肉注射的生物利用度为81.5%。结果显示多拉菌素在猪体内具有吸收分布较迅速、体内分布容积大、消除缓慢和生物利用度相对较高的特点,提示多拉菌素在猪体内作用的长效性主要由该化合物的自身特性所决定,而与给药途径和使用的溶剂关系不大,研究结果对指导临床正确用药具有重要意义。     

鸡传染性支气管炎病毒S1基因和鸡Ⅱ型干扰素基因在重组鸡痘病毒中的共表达

将鸡Ⅱ型干扰素（ChIFNγ）基因和鸡传染性支气管炎病毒S1基因同时插人到鸡痘病毒转移载体中，构建含有这2个基因的鸡痘病毒转移载体pSY—ChIFNγS1。采用脂质体法将该质粒转染鸡痘病毒感染的鸡胚成纤维细胞（CEF），经过8轮蓝斑筛选，得到纯化的能够同时表达鸡Ⅱ型干扰素和鸡传染性支气管炎病毒S1基因的重组鸡痘病毒rFPV—ChIFNγS1。rFPV—ChIFNγS1接种28日龄的SPF鸡1周后，可以检测到针对传染性支气管炎病毒S1基因的ELISA抗体，重组病毒接种鸡的CD4^＋、CD8^＋和γδTCR阳性T淋巴细胞的百分比含量显著高于非免疫对照鸡（P％0．05）；免疫4周后用传染性支气管炎LX4强毒株攻击，rFPV—ChIFNγS1免疫组仅有1只出现轻微的呼吸道症状（1／16），而非免疫对照组则有16只发病（16／16），并有2只出现死亡（2／16），表明rFPV—ChIFNγS1对接种鸡可以产生良好的保护效果。     

日粮中添加杜仲提取物对肉仔鸡生产性能的影响

选用825只艾维茵肉仔鸡,随机分为5组,每组5个重复,每个重复33只鸡。对照组饲喂基础日粮,试验组在基础日粮中分别添加1500,2000,2500g/t的杜仲提取物或50mg/kg的效美素,比较杜仲提取物对肉仔鸡生产性能及胴体品质的影响。试验分2个阶段(0～21d和21～42d),试验鸡自由采食和饮水。研究结果表明,1)日粮中添加杜仲提取物能降低采食量,提高肉仔鸡成活率,其中以添加1500g/t杜仲提取物效果较好。2)杜仲提取物能促进肌肉组织蛋白质的合成,降低体内脂肪的沉积,在一定程度上改善肉仔鸡胴体品质。     

利用血液蛋白及酶多态性分析技术鉴定山羊亲缘关系的研究

选择血红蛋白(Hb)、运铁蛋白(Tf)、亮氨酸胺肽酶(LAP)、前白蛋白3(Pa3)、淀粉酶(Amy)对可能为同卵双生波尔山羊的亲缘关系鉴定。结果发现，除淀粉酶(Amy)和亮氨酸胺肽酶(Lap)外，其余位点均有多态性。由蛋白位点的基因型判定羔1、羔2基因型完全一致，是供体后代的概率为75G，受体后代的概率为22．8％，从而确认羔1、羔2的双亲为供体公羊和供体母羊。     

几种绵羊常用粗饲料GI的测定及其代谢能模型化研究

在测定5类9种粗饲料及3个混合粗饲料的常规成分基础上,实测了它们的粗饲料分级指数(GI):大青山草地早熟禾3.4758、沙打旺3.3731、苜蓿1.7202、混粗C21.1797、青干草1.1029、混粗C10.7852、羊草0.5684、玉米青贮0.4152、玉米秸0.1985、谷草0.1728、混粗D0.0805、苏丹草0.0687,并就GI与饲料相对值(RFV)对粗饲料品质的分级进行了比较,表明GI要优于RFV,同时证明:GI还可以用于混合粗饲料的优化与牧草刈割期的确定。研究并建立了预测粗饲料代谢能(ME)的模型:ME(MJ/kg)=-11.7492 0.5959IVDM(D%)-0.0044[IVDM(D%)]2,其中IVDMD为体外干物质消化率。     

四倍体鸭茅产量及其构成因素的QTL定位

产量相关性状是复杂的数量性状,对鸭茅的单株产量及构成因素进行QTL分析,可提高育种中对产量性状优良基因选择的效率,同时为鸭茅遗传改良、基因克隆及分子标记辅助育种提供理论依据。以四倍体鸭茅“楷模”和“01436”为亲本杂交而成的作图群体为试验材料,于2014年对洪雅、宝兴两个不同生境下鸭茅株高、旗叶长、倒二叶长、旗叶宽、倒二叶宽、茎粗、花序长、分蘖数、单株干重等9个产量相关性状进行了表型鉴定及相关性分析。此外,在已构建的高密度鸭茅分子遗传图谱的基础上,采用MapQTL 5.0进一步对这些性状QTL定位分析。结果表明,绝大多数性状在亲本间呈显著差异且都整体表现出连续变异,符合数量性状遗传的特征;相关性分析表明,大多数产量相关性状均与干重极显著正相关,与单株干重相关性最好的依次为分蘖、株高;QTL分析发现,控制该9个农艺性状的QTL共60个,洪雅38个,宝兴22个,这些QTL分别定位于分子连锁图谱的1、2、3、4、5共5个连锁群上,单个QTL的贡献率为5.7%~24.7%,单个性状QTL个数为2~15个。其中,控制株高、花序长的QTL各12个,控制倒二叶长、茎粗的QTL各4个,控制旗叶宽、倒二叶宽的QTL各2个,控制单株干重的QTL有6个,影响分蘖的QTL为3个,与旗叶长相关的QTL最多15个。     

The complete mitochondrial genome and molecular phylogeny of Lueyang black-bone chicken

ABSTRACT

1. The objectives of the current study were to investigate the mitochondrial genome and molecular phylogeny of Lueyang black-bone chicken, and provide molecule base to preserve and explore the specific chicken strain.

2. Based on sequencing and clustering, the complete mitochondrial DNA map and sequences of Lueyang black-bone chicken were revealed, and two phylogenetic trees of Lueyang black-bone chickens based on D-loop sequences and the mitochondrial genome were constructed.

3. The results showed that the complete mitochondrial genome of Lueyang black-bone chickens is 16,784bp in size, consisting of 22 transfer RNA genes, two ribosomal RNA genes, 13 protein-coding genes, and one non-coding control region. The base composition of the complete mtDNA sequence is 30.28% for A, 23.78% for T, 32.42% for C, 13.52% for G. Additionally, 10 haplotypes of D-loop sequences in 32 Lueyang black-bone chickens were detected, which were distributed into 4 clades (A, B, C and E).

4. It was concluded that genetic diversity is wide in Lueyang black-bone chickens, and this strain has multiple maternal origins from different regions in China and neighbouring regions.     

Effect on Rendement Napole genotype on metabolic markers in Ossabaw pigs fed different levels of fat

We investigated effects of Rendement Napole (RN ) genotype on metabolic markers in Ossabaw pigs fed diets with different levels of dietary fat. Thirty‐two pigs, belonging to either the wild‐type (WT , rn⁺/rn⁺) or carrier (CAR , RN ^?/rn⁺) genotypes (n  = 16/genotype), were divided into two dietary groups, (high fat [HF ] or low fat [LF ]) diets, for 12 weeks (n  = 8 pigs/genotype/diet) after which pigs were killed for gene expression analysis by RT ‐PCR . Feeding HF diet caused increased daily gain (ADG , p  <  .05) and final body weight (BW ) (p  <  .05) in comparison with the LF diet (p  <  .05). Feed efficiency (gain:feed) was higher (p  <  .05) in pigs on the HF and was higher (p  <  .05) in CAR pigs compared to WT . There was genotype × diet interaction (p  =  .05) on final BW such that CAR animals on LF diet had the same final BW as animals of both genotypes on HF diet. Carrier pigs on LF diet had higher (p  <  .05) average daily gain and gain:feed than WT pigs. There was a trend (p  <  .08) for a higher feed consumption in pigs on the LF diet. Backfat thickness was higher (p  <  .01) in pigs on the HF diet. Serum triglyceride was higher (0.62 vs. 0.33 mg/dl, p  <  .01) in pigs on HF diet. Serum insulin was higher (p  <  .05) in CAR versus WT pigs (0.40 vs. 0.015 μg/ml). Pigs on the HF diet had a higher (p  <  .05) serum insulin compared to those on the LF diet (0.032 vs. 0.023 μg/ml). Carnitine palmitoyl transferase 1‐alpha was higher (p  <  .05) in the longissimus dorsi and semitendinosus muscles of pigs on HF diet. Acyl‐CoA oxidase I was elevated (p  <  .05) in the liver of pigs on HF diet. Fatty acid synthase was lower in the longissimus dorsi muscle, liver and mesenteric fat (p  <  .05) of carrier pigs. The RN gene regulates specific metabolic markers in the Ossabaw pigs.