耕作方式和秸秆覆盖对旱地麦豆轮作下小麦籽粒产量、蛋白质含量和土壤硝态氮残留的影响

为明确耕作方式和秸秆覆盖对旱地麦豆轮作下小麦籽粒产量、蛋白质含量和土壤硝态氮残留的影响,2014年10月-2016年6月,利用设置在豫西典型旱作区的麦豆轮作栽培模式长期定位试验,选取传统翻耕、翻耕覆盖、旋耕和旋耕覆盖4个处理,比较了小麦氮素吸收利用、籽粒产量、蛋白质含量以及土壤硝态氮残留量。结果表明,与翻耕相比,旋耕不影响小麦产量,但花后氮素积累量、籽粒蛋白质含量和蛋白质产量分别降低60.0%、8.6%和13.0%,而成熟期0~200 cm土层硝态氮残留量显著提高28.6%。同一耕作方式下,秸秆覆盖较无覆盖不仅显著提高了穗数、穗粒数、千粒重和收获指数,还提高了拔节前和开花后的氮素积累量,促进了营养器官氮素向籽粒中转运,从而使翻耕覆盖的籽粒产量、氮素吸收效率、籽粒蛋白质含量和蛋白质产量较翻耕分别提高11.5%、13.5%、7.4%和21.3%,旋耕覆盖较旋耕也分别提高23.0%、39.5%、12.8%和38.5%。在试验进行7年后的小麦成熟期,翻耕覆盖0~200 cm土层硝态氮残留量较翻耕降低31.3%,旋耕覆盖较旋耕也降低51.4%。因此,秸秆覆盖不仅可提高旱地麦豆轮作下小麦产量、蛋白质含量和氮素吸收效率,还能降低土壤硝态氮的残留量,是兼顾旱地小麦高产优质和环境友好生产的有效途径,尤其以旋耕覆盖效果突出。     

不同地区动物源致病性大肠杆菌的分子特性与表型分析

为进一步了解致病性大肠杆菌流行状况,减轻大肠杆菌对畜牧业和公共卫生的危害,对不同时间国内外报道的动物中分离的大肠杆菌,进行毒力、血清型、耐药性和基因型等方面的比较,对比分析大肠杆菌分子特性和表型差异,从而为临床医学和公共卫生控制提供指导。     

金安桥水电站初次蓄水对导流洞稳定性影响的计算分析

金安桥水电站下闸蓄水后，陡升的库水位将对导流洞结构稳定造成不利影响。为保障堵头封堵前的导流洞结构稳定性，运用三维弹塑性损伤有限元，在模拟进水口边坡及导流洞开挖支护的基础上，计算汛前下闸水位时的岩体渗流场，对导流洞围岩和衬砌在岩体渗流作用下的结构稳定性进行复核分析。分析结果表明，导流洞的围岩稳定性在蓄水后仍有保障，衬砌结构受力较小，现有环向配筋满足结构内力要求，但在进水口变截面和导流洞变截面部位沿水流方向的拉应力较大，使得衬砌出现开裂。进一步分析表明，上述区域的开裂范围有限，对整体衬砌结构影响较小。     

羊传染性脓疱病毒NZ2毒株CBP蛋白结构分析与表位预测

本研究应用生物信息学方法,以ORFV NZ2毒株的CBP蛋白氨基酸序列为研究对象,对CBP蛋白的理化特性、亲水性、跨膜区、信号肽、二级结构、三级结构、B细胞表位和T细胞表位进行了预测分析。结果显示,CBP蛋白的相对分子质量为31.179 89 kDa,理论等电点为4.68,半衰期为30 h,稳定系数为43.06,脂肪族指数为81.78,总平均亲水性为-0.383。CBP蛋白为亲水性蛋白,无跨膜区,不属于跨膜蛋白,存在信号肽;二级结构中α螺旋、β折叠、β转角、无规卷曲分别占38.11%、33.91%、5.94%和10.48%,三级结构形似倒立的哑铃,上下对称。筛选出了6个优势B细胞表位、3个CTL细胞表位,无Th细胞表位。CBP蛋白为亲水性膜外蛋白,细胞表位较少,在细胞膜外为ORFV逃避宿主免疫反应发挥作用。本研究为CBP蛋白的功能研究与ORFV的致病机制研究提供了理论依据。     

广西5种人工林地土壤微生物数量及土壤酶活性分析

为当地珍贵速生树种人工林的发展及合理利用提供理论依据。分析广西5种珍贵树种人工林土壤微生物数量及土壤酶活性差异,以相同立地条件下12年生的黑木相思(Acacia melanoxylon)、老排(Mytilaria laosensis)、红椎(Castanopsis hystrix)、黧蒴椎(Castanopsis fissa)和火力楠(Michelia macelurei)人工纯林为研究对象,采用稀释平板涂布法和土壤酶活性测定法,测定和分析该5种人工林地土壤微生物数量及酶活性。结果表明:5种林地的土壤微生物总数和细菌数量大小均为:火力楠黧蒴锥红椎黑木相思米老排。但5种林地的土壤酶活性大小不一,蔗糖酶、脲酶、蛋白酶、酸性磷酸酶活性在5种林地之间的差异极其显著,而过氧化氢酶活性不显著。5种林地中土壤酶活性相对较强的是米老排人工林,较弱的是黑木相思林和火力楠林。土壤酶活性与微生物数量的相关分析表明,土壤中蔗糖酶活性与放线菌数量呈极显著正相关关系,其余相关性没有达到显著水平。     

1株鸭源非O1/O139群霍乱弧菌的分离鉴定与致病性分析

为探明引起贵州省某鸭场雏鸭发病的病原及其致病性和耐药情况，本研究对该鸭场送的疑似细菌感染病鸭进行剖检，取鼻黏膜、心脏和肝脏等组织器官接种于培养基中进行细菌分离鉴定，通过对分离菌进行药敏试验、动物回归试验和毒力基因检测研究其耐药情况和致病性。结果显示，分离菌在血琼脂培养基上生长16 h后呈现为边缘整齐、有光泽的乳白色菌落，伴有β-溶血现象，经革兰氏染色后在生物显微镜下呈两端钝圆、弧状、排列无规则的革兰氏阴性短小杆菌，与霍乱弧菌相符；16S rDNA基因序列同源性及系统进化树显示，该分离菌与霍乱弧菌同源性高达99.6%~99.7%聚为一支；药敏试验结果显示，分离菌对大部分药物都表现为耐药，其中对氨苄西林、克林霉素、复方新诺明、苯唑西林和克林霉素等抗菌药耐药性较强，对头孢哌酮和头孢曲松敏感；动物回归试验显示，分离菌可导致试验组雏鸭5 d内全部发病死亡，表明该分离菌对雏鸭具有较强的致病性；毒力基因PCR检测结果显示，检测的霍乱弧菌相关毒力基因hlyA、ompW和chxA为阳性，而检测的O1群rfb、O139群rfb、tcpA及ctxA基因为阴性，表明本次分离的霍乱弧菌携带有致病基因，但不属于O1和O139血清群。结果表明，该鸭场雏鸭发病的疫情病原为非O1/O139血清群霍乱弧菌，该菌致病性强且对多种抗菌药物耐药。本试验结果为贵州省鸭霍乱弧菌病的防控提供了参考依据。     

南方地区高水分玉米安全度夏技术探讨

根据水分的高低,对新收购的高水分玉米分别储存在露天囤和高大平房仓中,将露天囤里的玉米通风降水后转入高大平房仓储存,再对玉米通风降温,并采取仓房密封、悬挂防晒网、空调控温等配套措施控制粮温,期间采取磷化铝多次补药熏蒸杀灭粮堆内害虫及霉菌,使玉米安全度夏。     

Expression,Purification and Activity Evaluation of Mb1230 Gene of Mycobacterium bovis

To explore the value of Mb1230 protein of Mycobacterium bovis in the diagnosis of bovine tuberculosis,we obtained the Mb1230 gene by PCR and constructed recombinant plasmid pET-22b-Mb1230.Recombinant Mb1230 protein was obtained by IPTG induction and purified by affinity chromatography.The activity of the recombinant protein was evaluated by TST test,IGRA test and indirect ELISA.The size of the recombinant protein matched with the theoretical value proved by SDS-PAGE;Western blotting result showed that the recombinant protein could react with mouse anti-His antibody,and had specific band;The results of TST test,IGRA test and indirect ELISA test also showed the recombinant protein had antigenic activity.The results indicated the recombinant protein Mb1230 had good B cell and T cell activity,so,it had the potential application in the diagnosis of bovine tuberculosis.     

5‐Aminolevulinic Acid Activates Antioxidative Defence System and Seedling Growth in Brassica napus L. under Water‐Deficit Stress

The present study assesses the effects of 5‐aminolevulinic acid (ALA, 0, 0.1, 1 and 10 mg l^?1) on the growth of oilseed rape (Brassica napus L. cv. ZS758) seedlings under water‐deficit stress induced by polyethylene glycol (PEG 6000, 0 and ?0.3 MPa). Water‐deficit stress imposed negative effects on seedling growth by reducing shoot biomass, cotyledon water potential, chlorophyll content and non‐enzymatic antioxidants (glutathione and ascorbic acid) levels. On the other hand, water‐deficit stress enhanced the malondialdehyde (MDA) content, reactive oxygen species (ROS) production, enzymatic antioxidants activities, reduced/oxidized glutathione ratio (GSH/GSSG) and reduced/oxidized ascorbic acid (ASA/DHA) ratio in seedlings. Application of ALA at lower dosages (0.1 and 1 mg l^?1) improved shoot weight and chlorophyll contents, and decreased MDA in rape seedlings, whereas moderately higher dosage of ALA (10 mg l^?1) hampered the growth. The study also indicated that 1 mg l^?1 ALA improved chlorophyll content, but reduced MDA content and ROS production significantly under water‐deficit stress. Lower dosages of ALA (0.1 and 1 mg l^?1) also enhanced GSH/GSSG and ASA/DHA as compared to the seedlings under water‐deficit stress. The antioxidant enzymes (ascorbate peroxidase, peroxidase, catalase, glutathione reductase and superoxide dismutase) enhanced their activities remarkably with 1 mg l^?1 ALA treatment under water‐deficit stress. It was also revealed that 1 mg l^?1 ALA treatment alone induced the expression of APX, CAT and GR substantially and under water‐deficit stress conditions ALA treatment could induce the expression of POD, CAT and GR to a certain degree. These results indicated that 0.1–1 mg l^?1 ALA could enhance the water‐deficit stress tolerance of oilseed seedlings through improving the biomass accumulation, maintaining a relative high ratio of GSH/GSSG and ASA/DHA, enhancing the activities of the specific antioxidant enzymes and inducing the expression of the specific antioxidant enzyme genes.