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961.
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对建立的一种鸡组织中磺胺氯吡嗪钠残留检测的高效液相色谱法进行复核验证。鸡组织样品中磺胺氯吡嗪钠残留经乙腈提取,正己烷去脂肪,MCX固相萃取小柱净化。采用高效液相色谱紫外检测器检测,流动相为乙腈-0.02mol/L磷酸二氢钾水溶液(35:65,V/V),紫外检测波长为272nm,外标法定量。结果显示,磺胺氯吡嗪钠标准工作液在0.04~20.0μg/mL范围内具有良好的线性关系(R^2=0.9999)。在鸡肌肉、肝脏、肾脏、皮脂各组织中添加浓度分别为40、100、200μg/kg时,各组织样品中磺胺氯吡嗪钠的回收率范围为74.70%~93.67%。磺胺氯吡嗪钠的检测限为20μg/kg,定量限为40μg/kg。复核验证的鸡组织中磺胺氯吡嗪钠残留检测高效液相色谱法可行,方法简便快捷,回收率高,适合鸡组织中磺胺氯吡嗪的残留检测。 相似文献
965.
Recently, flavonoids were shown to modulate the outcome of clubroot development in Arabidopsis thaliana after infection with the obligate biotrophic pathogen Plasmodiophora brassicae. Therefore, the development of clubroot disease was investigated in Arabidopsis after treatment with prohexadione‐calcium (ProCa), an inhibitor of ascorbic acid/2‐oxoglutaric acid‐dependent dioxygenases such as flavanone‐3‐hydroxylase. The treatment resulted in a reduction of the flavonols quercetin and kaempferol in clubroots, whereas the precursor naringenin highly accumulated. The root system of ProCa‐treated plants was better developed although galls were still visible. Thus, ProCa treatment resulted in reduced gall size. Flavonoids are thought to inhibit polar auxin transport by modulating auxin efflux carriers. It was investigated whether the auxin response might change as a consequence of the accumulation of naringenin in ProCa‐treated plants. In the areas of gall development an auxin response was indicated by the auxin‐responsive promoter DR5 coupled to the reporter β‐glucuronidase (GUS), whereas very little staining was found in healthy root parts. No differences in GUS activity were found between P. brassicae‐infected and ProCa‐treated plants, and plants only infected with P. brassicae, indicating that the effect of ProCa treatment on clubroot reduction is not via changes in auxin responses. As ProCa is also an inhibitor of late steps in gibberellin biosynthesis, a specific gibberellin biosynthesis inhibitor, chlormequatchloride (CCC), was tested on club development. However, CCC did not reduce disease symptoms, indicating that the observed reduced gall development was not because of gibberellin biosynthesis inhibition by ProCa. 相似文献
966.
Characterizations and molecular mapping of a novel dominant semi-dwarf gene Sdd(t) in rice (Oryza sativa) 总被引:1,自引:0,他引:1
By nitrogen ion implanting, we obtained a semi‐dwarf mutant from a japonica rice cultivar Y98148, designated as Y98149. The genetic analysis of Y98149 indicated that the semi‐dwarf phenotype was controlled by a single dominant gene, Sdd(t). We show that Y98149 reduced plant height mainly via inhibiting the first, second and third internode elongation. Based on this dwarfing pattern, the mutant could be grouped into dn‐type dwarf defined by Takeda [Gamma Field Symp. (1977) Vol. 16, PP. 1–18] . In addition, the Sdd(t) gene was sensitive to gibberellin (GA) based on the response to extraneous GA3 and the quantitative determination of endogenous GA1 and GA4. To map the Sdd(t) gene, we tested molecular markers by bulk segregant analysis. The Sdd(t) gene was localized to a 6.4 cM‐interval on the short arm of chromosome 6, flanked by two sequence‐tagged site markers S9 and S13. 相似文献
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本研究主要对口蹄疫病毒(FMDV) Hankou/99株全基因序列进行测定,通过基因序列分析,确定其基因型,丰富了FMDV基因库,为研究猪源FMDV的分子变异、感染性分子克隆及致病机理奠定基础.从感染FMDV Hankou/99株的细胞液中提取RNA,通过RT-PCR技术,获得猪FMDV Hankou/99分离株覆盖全基因组的5个cDNA片段(S、L、C、D、E),分别对这些片段进行克隆和序列测定.结果显示,FMDV Hankou/99株全基因组长8099 bp;5'NCR长1040 bp,开放阅读框长6966 bp;3'NCR长93 bp,其后是30个碱基的连续poly(A)结构.通过与参考株基因组结构比较分析,显示其在分类地位上属于O型FMDV,并与猪源FMDV毒株OLZ、TW/97同源性较高,特别是3A区域上都有30 bp的缺失.另外,通过与9个参考株的VP1系统发生树分析,显示其与OLZ、TW/97、O/Akesu/58、O/OMⅢ 4个毒株为同一基因型. 相似文献