叶面喷施不同浓度ALA对黄瓜幼苗抗氧化酶系统的影响

为了探讨叶面喷施5-氨基乙酰丙酸(ALA)在黄瓜苗期的施用浓度和效果,以黄瓜品种津春4号3叶1心期的幼苗为材料,研究了不同浓度ALA对黄瓜幼苗叶片光合色素含量和抗氧化酶系统的影响。试验结果表明,叶面喷施10、30、50 mg/L的ALA可明显提高黄瓜叶片叶绿素(Chl)和类胡萝卜素(Car)含量,降低Chl a/b比值;显著增加超氧化物歧化酶(SOD)、过氧化氢酶(CAT)、抗坏血酸过氧化物酶(APX)和过氧化物酶(POD)活性,脯氨酸和可溶性蛋白含量;降低超氧阴离子(O2-·)生成速率、过氧化氢(H2O2)和丙二醛(MDA)含量;当ALA浓度达100 mg/L时,黄瓜幼苗受到一定的氧化胁迫伤害。这些结果说明,喷施浓度不超过100 mg/L ALA可促进黄瓜幼苗叶片光合色素的合成、增加其抗氧化能力,降低膜脂过氧化的程度,综合各项指标,以30 mg/L的ALA叶面喷施浓度在黄瓜幼苗上效果最佳。     

基于SPEI_PM指数的渭河流域气象干旱时空演变特征

利用渭河流域25个气象站点1980−2018年月值气象数据集，基于Penman-Monteith蒸散模型计算多个时间尺度的标准化降水蒸散发指数（SPEI），分析渭河流域气象干旱的演变、趋势、影响范围、发生频率和持续时间等时空变化特征，以期为渭河流域防灾减灾管理提供科学依据。结果表明：（1）近39a来渭河流域有明显的干湿周期变化，但整体上呈变干的趋势，干旱时段主要集中在1995−2009年，其中以2000−2009年的干旱站次比最大，平均达到36%，且干旱持续时间最长，约3.6个月，1980−1989年干旱持续时间最短，约1.6个月；（2）渭河流域秋季总体呈湿润变化趋势，而春季和夏季干旱在不断加剧，是区域年际干旱的主要驱动力；（3）渭河流域干旱以危害性较小的轻中旱为主，但2000年前后出现严重及极端干旱的站次相对较多，其中1997年研究区内发生的干旱程度较高，影响范围较广；（4）不同时间尺度各等级干旱发生频率的变化规律表现一致，均呈现出干旱等级越高发生频率越低的态势，且极端干旱在年际尺度内发生次数较为频繁，从空间上看渭河流域东北部是干旱多发区。总之，近39a来渭河流域总体干旱较为严重的时段为2000−2009年，且研究区内干旱呈北重南轻特征，因此北部地区仍需加强防灾管理。     

光周期对北京油鸡雏鸡采食行为与生长性能的影响

为研究光照周期对北京油鸡雏鸡采食行为与生长性能的影响,本试验选择1日龄北京油鸡162只,随机分为三个处理(1、2、3),每处理54只,设3个重复,每个重复18只。1~3日龄均采用23L∶1D的光周期,4日龄起三个处理的光周期分别设置为8L∶16D、12L∶12D、16L∶8D,自雏鸡2周龄开始试验,6~7周龄观察记录各处理目标鸡的采食行为,并记录2~7周龄生长性能。结果表明:采食频次各处理间差异不显著(P>0.05),但处理2、3比处理1呈增加趋势;采食行为的最大、最小与平均持续时间处理3显著大于处理1(P<0.05),处理1和处理2之间无显著差异(P>0.05);采食在所有观测行为中所占时间比例均表现为处理3显著大于处理1(P<0.05),3个处理分别为18.41%、21.5%和24.74%。5周龄后采食量均为处理3显著高于处理1、2(P<0.05),7周龄日增重处理3显著高于处理1、2(P<0.05),而料肉比则在第6~7周龄时处理1显著低于处理3(P<0.05),其它各周各处理间无显著差异(P>0.05)。因此,北京油鸡雏鸡(7周龄前)在16L∶8D光周期下比12L∶12D、8L∶16D的采食时间长,利于雏鸡的采食量和体重的增加,但8L∶16D时的饲料利用效率比16L∶8D高。     

番鸭产蛋各期肝脂肪酸组成及AMPK信号通路基因表达研究

旨在探究产蛋各期番鸭肝腺苷酸活化蛋白激酶（AMPK）信号通路基因表达和肝脂肪酸组成,为番鸭肝脂质代谢应答产蛋提供机理研究。本研究选取开产前22周龄、产蛋初期30周龄、产蛋中期40周龄和产蛋末期60周龄母番鸭各15羽,全自动生化仪测定血脂水平,苏木精-伊红（HE）染色和油红O染色观察肝组织学结构,实时荧光定量PCR （qRT-PCR）检测肝AMPK通路基因表达,气相色谱-质谱联用法（GC-MS）检测产蛋各期肝脂肪酸组成。结果表明,总胆固醇（TC）、低密度脂蛋白胆固醇（LDL-C）、甘油三酯（TG）和极低密度脂蛋白胆固醇（VLDL-C）水平在40周龄显著高于22、30和60周龄（P<0.05）;高密度脂蛋白胆固醇（HDL-C）水平在30和40周龄显著低于22和60周龄（P<0.05）。肝HE和油红O染色切片显示,肝在22周龄呈实质状,至产蛋40和60周龄,肝脂滴沉积明显（P<0.05）。AMPKα1在22、30、40和60周龄呈本底低水平表达,并显著低于产蛋各期肉碱脂酰转移酶1（CPT1）和脂肪酸合成酶（FAS）的表达量（P<0.05）,FAS在22、40和60周龄均呈高水平表达（P<0.05）;羟甲基戊二酰辅酶A还原酶（HMGR）、肝细胞核因子4α（HNF4α）、乙酰辅酶A羧化酶1（ACC1）和固醇调控元件结合蛋白-1（SREBP1c）在40周龄表达量显著高于22和30周龄（P<0.05）。肝中饱和脂肪酸（SFA）、单不饱和脂肪酸（MUFA）和多不饱和脂肪酸（PUFA）主要由C16∶0、C18∶0、C18∶1和C20∶2 n-6构成,分别占总脂肪酸含量的32%、16%、30%和9%。C14∶0和C16∶0含量在40周龄显著高于22周龄（P<0.05）;C24∶0、C20∶2 n-6和PUFA含量在60周龄显著高于22和40周龄（P<0.05）。综上,番鸭产蛋期肝通过上调FAS等脂质合成基因表达,合成大量长链脂肪酸,沉积于肝,并增加血脂水平。     

丁酸梭菌在家禽生产中应用的研究进展

丁酸梭菌作为一种益生菌,存在于人和动物的肠道中,不易受到胃酸、消化酶和胆汁酸等因素的影响,不仅可以通过把营养物质降解成丁酸为动物提供营养与能量,而且可以保护肠道健康,促进营养物质的吸收和动物的生长,以及增强免疫功能等,因此丁酸梭菌可以作为饲料添加剂用于畜禽生产。本文对丁酸梭菌对家禽生理、生产性能的影响及其机制进行综述,以便为丁酸梭菌在家禽生产中的应用提供参考。     

两种无抗制剂对育肥猪生长性能及肠道健康的影响

本试验通过在生长育肥猪饲粮中添加两种不同的无抗制剂,探究其对育肥猪生长及肠道健康的影响。选取体重为（85.95±3.48） kg的LDY三元杂交猪60头,分为对照组、试验1、2组,每组5个重复,每个重复4头猪（阉公猪和母猪各半）。对照组饲喂基础饲粮,试验1组在基础饲粮中添加0.5%的红曲合生元酵母硒锗复合制剂,试验2组在基础饲粮中添加0.5%的复方中药提取物。结果表明：①3组间生长性能各项指标均差异不显著（P>0.05）。②与对照组相比,试验1组空肠的绒毛高度（VH）、绒毛高度/隐窝深度（V/C）以及回肠的绒毛高度均显著增加（P<0.05）,试验2组空肠和回肠的绒毛高度均显著增加（P<0.05）;试验1组空肠和回肠的绒毛高度显著高于试验2组（P<0.05）。③与对照组相比,试验1和2组盲肠菌群香浓指数均显著升高（P<0.05）、辛普森指数均显著降低（P<0.05）;试验1组的香浓指数显著高于试验2组（P<0.05）。④在门水平上,与对照组相比,试验1组盲肠菌群变形菌门和放线菌门丰度均显著升高（P<0.05）,厚壁菌门丰度显著降低（P<0.05）;试验2组厚壁菌门和变形菌门丰度显著升高（P<0.05）,拟杆菌门丰度显著降低（P<0.05）;试验1组放线菌门丰度显著高于试验2组（P<0.05）,厚壁菌门丰度显著低于试验2组（P<0.05）。在属水平上,与对照组相比,试验1组链球菌属丰度显著升高（P<0.05）,苏黎世杆菌属、uncultured_bacterium_f_Muribaculaceae和乳杆菌属丰度显著降低（P<0.05）;试验2组瘤胃菌属和链球菌属丰度显著升高（P<0.05）,苏黎世杆菌属、梭菌属_13、乳杆菌属丰度显著降低（P<0.05）;试验1组梭菌属_13和链球菌属丰度显著高于试验2组（P<0.05）,试验1组uncultured_bacterium_f_Muribaculaceae、瘤胃菌属显著低于试验2组（P<0.05）。⑤试验1组Occludin、Zo-1、Claudin-1表达量显著高于对照组（P<0.05）,Occludin、Claudin-1表达量显著高于试验2组（P<0.05）。以上结果表明,红曲合生元酵母硒锗复合制剂和复方中药提取物对育肥猪肠道健康均有改善作用,但红曲合生元酵母硒锗复合制剂组饲喂效果优于复方中药提取物组。     

Oxidative stress drives divergent evolution of the glutathione peroxidase (GPX) gene family in mammals

The molecular basis for adaptations to extreme environments can now be understood by interrogating the ever-increasing number of sequenced genomes. Mammals such as cetaceans, bats, and highland species can protect themselves from oxidative stress, a disruption in the balance of reactive oxygen species, which results in oxidative injury and cell damage. Here, we consider the evolution of the glutathione peroxidase (GPX) family of antioxidant enzymes by interrogating publicly available genome data from 70 mammalian species from all major clades. We identified 8 GPX subclasses ubiquitous to all mammalian groups. Mammalian GPX gene families resolved into the GPX4/7/8 and GPX1/2/3/5/6 groups and are characterized by several instances of gene duplication and loss, indicating a dynamic process of gene birth and death in mammals. Seven of the eight GPX subfamilies (all but GPX7) were under positive selection, with the residues under selection located at or close to active sites or at the dimer interface. We also reveal evidence of a correlation between ecological niches (e.g. high oxidative stress) and the divergent selection and gene copy number of GPX subclasses. Notably, a convergent expansion of GPX1 was observed in several independent lineages of mammals under oxidative stress and may be important for avoiding oxidative damage. Collectively, this study suggests that the GPX gene family has shaped the adaption of mammals to stressful environments.     

Construction and Identification of Yeast Surface Display Libraries of Ovis aries DRA Gene Exon 2

The specific primers were designed according to Ovis aries DRA gene sequence deposited in GenBank and the multiple cloning site of the plasmid pYD1,which was a vector used for protein surface display on Saccharomyces cerevisiae.The gene encoding DRA was amplified by PCR using the genomic RNA of Ovis aries.The 762 bp fragment was cloned and released in GenBank and registration number was KR422362.The PCR product was inserted into the yeast surface display plasmid vector pYD1 by double enzyme digestion.It was indicated that DRA gene was successfully integrated into the genome.Dot mutation was made at both ends of exon 2 in DRA gene for making restriction enzyme cutting site and design the exon 2 specific primers according to mutated Ovis aries DRA gene sequence.Sequenced exon 2 amplification products based on DNA pooling of sheep large sample template was analyzed the polymorphic loci.The polymorphic exon 2 246 bp fragment was obtained by double enzyme digestion and connected to surface display restructuring mutation carriers pYD1-DRA by the same double enzyme digestion,and then we successfully constructed yeast surface display libraries.We transformed it into Saccharomyces cerevisiae EBY100 cell.Yeast monoclone was identified by PCR amplification and sequencing,and we confirmed that DRA gene had been integrated into Saccharomyces cerevisiae genome.After galactose induced,it was detected that DRA gene library had been successfully demonstrated on the yeast cell surface under the fluorescence microscope by immunofluorescence method.     

Screening of Probiotics Inhibiting E. coli K88 in vitro

The probiotics tested in the experiment were isolated from the intestinal of weaning piglets.The isolated probiotics and E.coli K88 were inoculated into the culture of intestinal porcine epithelial cell-1 (IPEC-1).The activity of lactate dehydrogenase (LDH) in the supernatant was measured after incubating for 2.5 h.At the same time, the probiotics and E.coli K88 were co-cultured in vitro, the number of E.coli K88 was counted and the probiotics which could be resistant to the E.coli K88 were selected 2.5 h later.The results showed that the Lactobacillus casei and Bacillus coagulans could significantly reduce LDH activity (P<0.05), decrease the damage of E.coli K88; Bacillus coagulans could inhibit the growth of E.coli K88.At the same time, Bacillus coagulans could resist high temperature, acid and bile salt.The results showed that Bacillus coagulans strains had great potential as the application of probiotics strains.The methods could be used as a model of screen probiotics which could inhibit the growth of E.coli K88 in vitro.