一株抑草真菌发酵液中的抑草成分分析

为了鉴定从桉树根际筛选到的微生物的抑草潜力和抑草成分,以桉树根际土壤中筛选到的一株真菌为材料,利用生物测试验证菌株发酵液的抑草潜力,利用GC-MS对菌株发酵液抑草成分进行验证。结果表明,不同浓度菌株发酵液对稗草的根长、株高和干重都有显著的抑制作用,对稗草根长抑制率最大为稀释50倍时,抑制率为7.55%;对稗草株高和干重抑制率最高为原液,抑制率分别为56.53%和25.46%。GC-MS鉴定共检测到86个物质,含氮化合物最多,占59.10%,其次为羧酸及酯类化合物,占19.26%。抑草物质生物测试结果表明,邻香豆酸、柠檬醛和胡椒碱在低浓度时对莴苣的根长和株高都有很强的抑制作用。表明该菌株能够产生多种化感物质的结构类似物,使得菌株发酵液具有很强的抑草作用,具有开发为微生物除草剂的潜力。     

健康奶牛肠道中乳酸菌的分离与鉴定

在奶牛饲料中添加优良的乳酸菌微生物制剂对于生产实践有着重要的意义。由于奶牛肠道中的乳酸菌本身已适应奶牛肠道中的环境,并且与奶牛肠道中的致病菌长期拮抗竞争,因而是奶牛饲料中添加益生菌株的最佳来源。本试验利用改良MRS培养基从20头健康的荷斯坦泌乳牛粪便中进行菌群的分离鉴定,采用16S rRNA基因序列对分离的乳酸菌进行鉴定。最终获得瘤胃乳杆菌、乳酸乳球菌等18株乳酸菌。该试验中分离得到的乳酸菌为多角度开发我国乳酸菌资源和微生态制剂在畜牧生产中的应用奠定基础。     

中药复方舒肤膏质量标准研究

采用薄层色谱法对荆芥、防风、凌霄花和狼毒进行定性鉴别,采用高效液相色谱法对中药复方舒肤膏的有效成分梣酮和黄柏酮进行含量测定。结果表明,薄层色谱法结果理想,阴性样品无干扰;在5.92～47.36μg/mL梣酮与峰面积线性关系良好(r=0.999 1),平均回收率为99.76%(RSD=1.34%),在10.2～81.6μg/mL黄柏酮与峰面积线性关系良好(r=0.999 0),平均回收率为99.89%(RSD=1.63%),表明该方法操作简便,专属性好,准确可靠,可用于中药复方舒肤膏的质量控制。     

豆科全基因组DGAT 基因家族的鉴定与进化分析

本文运用生物信息学方法在12个豆科植物基因组中对DGAT（甘油二酯酰基转移酶）基因进行了全基因组鉴定，发现在四倍体花生和大豆基因组中含有的基因拷贝数相对较多，分别为17、10，这可能是导致其油脂合成能力高于其他作物的重要因素。通过对家族基因进行系统发育分析，发现DGAT 基因在真双子叶植物分化之前已存在，在豆科植物中经历反复的全基因组加倍，使得家族得到扩张；并且串联重复对于家族扩增起到了不可忽视的作用，如葡萄中的两个旁系同源基因，由于串联重复使得基因拷贝数量提高了150%。大豆中DGAT 基因在不同的组织中表达模式与其系统发育关系也表现出了关联性。该基因家族相对保守，与豆科基因组进化基本保持了一致的进化速率。本研究对于认识豆科植物DGAT 基因进化过程具有重要的理论意义，同时在基因组学水平为大豆、花生等油脂合成品质改良提供了理论支撑。     

茶红素分离及稳定性研究

采用茶汤有机试剂萃取分离,并分别经过反相C_(18)柱层析纯化,制备出乙酸乙酯层、正丁醇层和酸性正丁醇层三部分茶红素。根据紫外可见光波扫描计算出色价,并研究了茶红素在不同条件下的稳定性。结果表明,30%、50%和70%甲醇梯度洗脱,纯化后3类茶红素液相检测发现无咖啡碱和茶黄素,仅有少量儿茶素杂质。纯化后色素色价分别为乙酸乙酯层128.04,正丁醇层91.04,酸性正丁醇层76.16。遮光处理,p H=3酸性条件,45℃以下贮藏,有利于茶红素的稳定性。     

Tagging quantitative trait loci for heading date and plant height in important breeding parents of rice (Oryza sativa)

Heading date and plant height are important determinants for plant growth rate. In this study, simple sequence repeat markers were used to tag quantitative trait loci (QTL) using a recombinant inbred line mapping population derived from two important breeding parents, genetic stock Kaybonnetlpa1-1 and indica cultivar Zhe733, using data collected under field and greenhouse conditions. Interval mapping, composite interval mapping, and multiple interval mapping were performed to map QTL for heading date and plant height, and to identify epistatic interactions between the QTL. qHD3.1 on chromosome 3 from KBNTlpa1-1 had the largest effect on heading date contributing an average of 28.4 % of the total phenotypic variation. qHD7.1, 7.2, and 8.1 also had a significant contribution to heading date from Zhe733 averaging 8.1, 12.8, and 12.8 % of the phenotypic variance, respectively, and there was a positive additive-by-additive epistatic interaction between qHD7.1 and qHD8.1. QTL, qPHT1.1 and qPHT3.1, for plant height were detected on chromosomes 1 and 3, respectively. qPHT1.1 contributed the largest effect representing 38.2 % of the total phenotypic variation. Comparison of the QTL identified in our study with previous results revealed that the chromosomal locations for QTL coincided closely with positions reported previously in other rice populations worldwide, suggesting that these QTL have coevolved and become domesticated. The tightly linked SSR markers that flank these QTL should be desirable for tagging heading date and plant height genes and facilitating their incorporation into advanced breeding lines using marker assisted selection.     

Acaricidal activity of extracts of neem (Azadirachta indica) oil against the larvae of the rabbit mite Sarcoptes scabiei var. cuniculi in vitro

The acaricidal activity of the petroleum ether extract, the chloroform extract and the acetic ether extract of neem (Azadirachta indica) oil against Sarcoptes scabiei var. cuniculi larvae was tested in vitro. A complementary log-log (CLL) model was used to analyze the data of the toxicity tests. The results showed that at all test time points, the petroleum ether extract demonstrated the highest activity against the larvae of S. scabiei var. cuniculi, while the activities of the chloroform extract and the acetic ether extract were similar. The activities of both the petroleum ether extract and the chloroform extract against the larvae showed the relation of time and concentration dependent. The median lethal concentration (LC(50)) of the petroleum ether extract (1.3muL/mL) was about three times that of the chloroform extract (4.1muL/mL) at 24h post-treatment. At the concentrations of 500.0muL/mL, the median lethal time (LT(50)) of the petroleum ether extract and the chloroform extract was 8.4 and 9.6h, respectively.