不同浓度褪黑素对氯化钠胁迫下宝岛蕉幼苗的影响

为了研究不同浓度褪黑素对宝岛蕉幼苗氯化钠胁迫的影响,使用不同浓度褪黑素处理宝岛蕉幼苗叶片,研究处理后宝岛蕉幼苗叶片和根系的可溶性糖、丙二醛、脯氨酸含量及叶质膜透性的变化。结果表明,褪黑素100μmol/L能够降低宝岛蕉幼苗叶质膜透性,提高叶片和根系可溶性糖含量,降低叶片和根系丙二醛含量,提高叶片和根系脯氨酸含量,提高幼苗耐盐性,以缓解氯化钠胁迫对宝岛蕉幼苗的伤害。     

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。     

青海湖裸鲤TOB1和TOB2基因的克隆与表达分析

【目的】对青海湖裸鲤TOB1和TOB2基因进行克隆及表达分析,为揭示其在青海湖裸鲤生长和生理过程中的作用奠定基础。【方法】采用PCR和RACE技术克隆青海湖裸鲤中TOB1和TOB2基因的cDNA全长序列,对其特性进行了生物信息学分析。以β-actin为内参基因,采用实时荧光定量PCR法(qRT-PCR)检测TOB1和TOB2基因在3龄成鱼肾脏、肠、鳃、脑、心脏、肌肉等组织及发育12,72,120,168,216 h胚胎中的表达水平。【结果】青海湖裸鲤TOB1 cDNA全长为1 734 bp,5′非编码区为466 bp,3′非编码区为296 bp,开放阅读框长972 bp,编码323个氨基酸。TOB2 cDNA全长为2 785 bp,5′非编码区为51 bp,3′非编码区为1 582 bp,开放阅读框为1 152 bp,编码383个氨基酸。TOB1和TOB2在N端均具有明显的BTG家族结构域,且系统进化分析显示2个TOB蛋白与鲤科鱼类同源性较高,亲缘较近。qRT-PCR结果表明,TOB1和TOB2在3龄成鱼的肾脏、肠、鳃、脑、心脏、肌肉等组织中均有表达;TOB1在3龄成鱼的心脏组织中表达量最高,其次为脑和肌肉组织,在鳃组织中的表达量最低;TOB2在3龄成鱼的脑组织中表达量最高,其次为肌肉。TOB1及TOB2在不同发育时期胚胎中均有表达,且都在12 h胚胎中表达量最高。【结论】TOB1及TOB2在3龄成鱼各个组织及胚胎中均有表达,但表达量有较大差异,表明2个基因均具有时空表达特异性。     

Ethyl acetate fraction of flavonoids from Polygonum hydropiper L. modulates pseudorabies virus-induced inflammation in RAW264.7 cells via the nuclear factor-kappa B and mitogen-activated protein kinase pathways

Pseudorabies virus (PRV) infection leads to severe inflammatory responses and tissue damage, and many natural herbs exhibit protective effects against viral infection by modulating the inflammatory response. An ethyl acetate fraction of flavonoids from Polygonum hydropiper L. (FEA) was prepared through ethanol extraction and ethyl acetate fractional extraction. An inflammatory model was established in RAW264.7 cells with PRV infection to evaluate the anti-inflammatory activity of FEA by measuring cell viability, nitric oxide (NO) production, reactive oxygen species (ROS) release, and mRNA expression of inflammatory factors, inducible nitric oxide synthase (iNOS), and cyclooxygenase-2 (COX-2). Its functional mechanism was investigated by analyzing the phosphorylation and nuclear translocation of key proteins in the nuclear factor-kappa B (NF-κB) and mitogen-activated protein kinase (MAPK) signaling pathways. Our findings indicate that PRV induced inflammatory responses in RAW264.7 cells, and the responses were similar to that in lipopolysaccharide (LPS)-stimulated cells. FEA significantly suppressed NO synthesis and down-regulated both expression and secretion of COX-2, iNOS, and inflammatory cytokines (P<0.05 or P<0.01). FEA also reduced NF-κB p65 translocation into the nucleus and decreased MAPK phosphorylation, indicating that the NF-κB/MAPK signaling pathway may be closely related to the inflammatory response during viral infection. The findings suggested the potential pharmaceutical application of FEA as a natural product that can treat viral infections due to its ability to mitigate inflammatory responses.     

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.     

海水中规模化培养西藏拟溞的技术优化研究

为了给北方海水鱼虾蟹类育苗增添一种新的生物活饵料,利用循环水培养装置研究了西藏拟溞Daphniopsis tibetana Sars在稀释海水(盐度为18~20)中规模化培养的技术工艺参数,即起始放养密度、充纯氧和日采收率。结果表明:起始放养密度对西藏拟溞种群增长和日产量影响显著(P0.05),不同起始放养密度(200、550、900、1250 ind./L)培养试验中,放养密度为1250ind./L时,培养第33天时种群密度达最高,为(9500±550.73)ind./L,平均日产量为(125.00±8.35)g/(m3·d);充纯氧与充空气相比较,充纯氧能显著提高种群密度和日产量(P0.05),当放养密度为1250 ind./L、充纯氧时,西藏拟溞种群密度最高达(11 600±560.45)ind./L,平均日产量为(156.82±8.49)g/(m3·d);日采收率对西藏拟溞的种群增长和日产量也有显著影响(P0.05),日采收率为20%时最佳,放养密度为1250ind./L、日采收率为20%时,西藏拟溞种群密度最高为(12 900±995.04)ind./L,平均日产量为(176.52±15.08)g/(m3·d)。     

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.