有益菌根真菌及其互作对带叶兜兰试管苗生理生长的影响

为探讨菌根真菌的互作效应,筛选协同互作模式组合,对从野生兜兰新鲜营养根中分离、筛选出的3种菌根真菌（PF02、PF06和PF07）,采用单菌接种、双菌混合接种和三菌混合菌种等7种接种方式,开展菌−苗共生培养,筛选出优势菌株PF02和PF07,揭示在实验室环境下接菌方式与接种效应之间的相互联系,分析菌根真菌互作对带叶兜兰植株生长和生理的影响。结果表明：显示菌根真菌互作对宿主植株的生物量、保护酶活性及叶绿素总量具有较好的正向效应。3种双菌混合接种方式PF02−PF06、PF02−PF07及PF06−PF07均能有效促进带叶兜兰生物量增长,尤其是PF02−PF06接种方式,抗氧化酶POD、超氧化物歧化酶SOD、过氧化氢酶CAT活性及叶绿素总量提高显著。选择优化的接种方式,以及能够协同促进、达到共生平衡的最佳接种方式组合,最大限度发挥菌根对宿主植物的益生作用。     

美国车厘子组织培养试验

采用美国思加图车厘子室内盆栽萌发的嫩芽和老芽作为外植体,分析不同处理时间对车厘子外植体萌芽效果的影响;采用不同浓度的植物生长调节剂对其进行诱导增殖和生根培养,筛选最佳组培方法。结果表明：嫩芽是车厘子外植体的最佳选择,通过7 s酒精和0.1%升汞9 min消毒获得无菌体,污染率低、褐化率较低、萌芽率60%。芽诱导培养基为MS+6-BA 1.0 mg/L+NAA 0.2 mg/L,增殖系数为3.92。生根培养基为1/2MS+NAA0.6 mg/L,生根率为100%。移栽炼苗基质比例为V（腐殖土）∶V（红土）=4∶6,盖膜驯化,保湿温度（25±2）℃,湿度80%,成活率达90%以上。     

大花蕙兰幼苗叶片诱导类原球茎

以大花蕙兰无菌幼苗叶片为外植体,成功诱导类原球茎(PLB).叶片部位是影响诱导的关键,只有叶片基部片段能成功诱导出PLB.不同激素配比以及外植体来源对PLB诱导有重要的影响.低浓度的2,4-D和较高浓度的6-BA对于拟球茎诱导PLB具有显著的促进作用.当2,4-D浓度高于0.6 mg/L时,PLB诱导受到显著抑制.较高的2,4-D水平可能有利于PLB诱导初始阶段,但不利于PLB诱导中后期的进一步发育.不同基因型有不同的最佳激素组合.添加0.2 mg/L的NAA对大花蕙兰PLB诱导没有显著影响,但在有的基因型中对PLB诱导有促进作用.以叶片基部片段诱导大花蕙兰PLB是可行的,为转基因研究提供了再生技术基础.     

南帕斯凝析油卸船的安全措施

针对南帕斯凝析油接卸作业过程中易产生较高含量有毒气体的问题,分析了凝析油的基本性质和硫化物分布情况,以识别其有毒气体成分.描述了接卸作业前和码头接卸作业两个阶段的注意事项:接卸作业前应对各个作业环节进行风险识别,制定应急方案,并确保设备完整;码头接卸作业前先进行作业准备,划定作业警戒区且保证消防通道畅通,接卸作业时,持续进行硫化氢检测,接卸作业后,及时对管道进行置换.最后,指出检尺口和卸船舱口为主要泄漏风险部位,提出了解决措施.     

高酸值米糠油酶法酯化脱酸研究

对脂肪酶Novozym 435催化高酸值米糠油酯化脱酸进行了研究.利用响应面分析法(RSM)优化脱酸条件.根据Box-Benhnken中心组合试验设计原理对试验条件进行优化,在分析各因素显著性及其交互作用的基础上,得出米糠油酯化脱酸最佳工艺参数为:酶质量分数1.1％、甘油添加量0.42 mg、温度56.4℃、反应时间23.2 h.实际测得脱酸后米糠油酸值(KOH)由56 mg/g降为5.04 mg/g,游离脂肪酸酯化率达到91％,与模型预测值基本相符.     

双胍盐对柑桔青霉病防治效果试验

两年的抑菌、刻伤接种和果实贮藏试验表明,双胍盐对柑桔青霉病的防治效果与伊迈唑相接近,可作为苯并咪唑类的替换药剂。     

动物、动物产品药物残留及应对措施

动物性食品中的药物残留量虽然很低,但对人体健康的潜在危害却甚为严重,对畜牧业生产影响巨大,而且影响深远,是国内外普遍关注的     

不同品系西方蜜蜂基因组DNA多态性图谱构建及杂交分析

本研究应用随机引物K（5'-CGGCCCCTGT-3'）对不同品系西蜂的基因组DNA扩增，获得了能区分不同品系西蜂的多态性DNA图谱，从多态性图谱中选取一个共同片段K1680bp，标记成探针，探针K1680bp与不同品系西蜂的基因组DNA匀有杂交，从而证明片段K1680bp是西蜂蜂种的共性，为西蜂的鉴定提供了直接依据。     

Protective effect of vitamin C and lycopene on the in vitro fertilization capacity of sex-sorted bull sperm by inhibiting the oxidative stress

The fertilization capacity of sex-sorted sperms is seriously decreased, which inhibits its wide application. However, little information is still available about the effect of vitamin C (VC) and lycopene (Lyc) on the fertilization capacity of sex-sorted bull sperm. In this study, the washing medium and fertilization medium of sex-sorted sperm from three bull individuals were supplemented with different concentrations of VC (0, 1 × 10^–3, 1 × 10^–4, 1 × 10^–5, 1 × 10^–6 M) or Lyc (0, 1 × 10^–4, 1 × 10^–5, 1 × 10^–6, 1 × 10^–7). After washing twice and incubation for 1.5 hr, the malondialdehyde (MDA) level, phosphatidylserine (PS) translocation, membrane potential (Δψm) and IVF (in vitro fertilization) ability of sex-sorted sperm were investigated. For the sex-sorted sperm of bulls A, B and C, 1 × 10^–3 M VC or 1 × 10^–4 M Lyc treatment significantly decreased their MDA levels and PS translocation and increased their Δψm levels and cleavage rates after IVF. When blastocysts were concerned, 1 × 10^–4 M Lyc significantly improved the blastocyst rates and their IFN-tau expression of bulls A and C. In conclusion, supplementation of 1 × 10^–3 M VC or 1 × 10^–4 M Lyc in washing and fertilization medium contributed greatly to improving the fertilization capacity of sex-sorted bull sperm during IVF procedure.     

Regulation of fibroblast growth factor 9 on the differentiation of goat intramuscular adipocytes

It has been found that fibroblast growth factor receptor (FGF-FGFR) signaling can regulate the expression of adipocyte differentiation genes. FGF9 is one of the members of FGFs that mainly binds receptors FGFR2 and FGFR3. FGF9 is highly expressed in the adipose tissue of humans and mice, but there are few reports on the role of FGF9 in goat intramuscular adipocyte differentiation. Therefore, this study explored the effect of FGF9 on adipocyte differentiation through cell culture, interference, and overexpression. The expression of receptors FGFR1–FGFR4 in adipocyte differentiation and their effects on differentiation were detected to screen receptor gene of FGF9. Finally, the interaction between FGF9 and the receptor was tested by cotransfection. Our results showed that FGF9 interacts with FGFR2 to inhibit goat intramuscular adipocyte differentiation by regulating peroxisome proliferator-activated receptor gamma (PPARγ) and preadipocyte factor 1 (Pref1), which is a data support for subsequent pathway research.