内蒙古高原紫花苜蓿土壤氮素丰缺指标和推荐施氮量

为了给内蒙古高原紫花苜蓿（Medicago sativa L.）测土施氮奠定科学基础，本研究采用“零散实验数据整合法”和“养分平衡-地力差减法”新应用公式，开展了该自然区域紫花苜蓿土壤氮素丰缺指标和推荐施氮量研究。结果表明：内蒙古高原生长第1年紫花苜蓿土壤碱解氮第1~6级丰缺指标为≥48，20~48，8~20，4~8，2~4和<2 mg·kg^-1，土壤全氮第1~5级丰缺指标为≥1.4，0.8~1.4，0.4~0.8，0.2~0.4和<0.2 g·kg^-1，土壤有机质第1~6级丰缺指标为≥17，10~17，6~10，3~6，2~3和<2 g·kg^-1。当紫花苜蓿目标产量9~18 t·hm^-2、氮肥利用率40%时，内蒙古高原紫花苜蓿第1~6级土壤推荐施氮量分别为0，68~135，135~270，203~405，270~540和338~675 kg·hm^-2。     

花生壳黄酮的提取纯化工艺

本文采用酶法预处理结合超声波辅助提取的方式，最大程度地提高了花生壳总黄酮的得率，并优化大孔树脂纯化工艺，提高了有效成分的纯度。花生壳黄酮的最佳提取工艺为：花生壳粉与水混合，半纤维素酶与木聚糖酶按1:1（m/m）复配，用量0.25‰，50℃酶解30 min后，按料液比1:20（m/V）加入乙醇至终浓度60%，于功率1000 W，55℃超声波辅助提取60 min，花生壳总黄酮的得率约为2.5%。选用D101型大孔树脂，上样缓冲液为pH 5.0的60%乙醇溶液，洗脱液为pH 10.0的70% 乙醇溶液，上样与洗脱流速为0.75 BV/h和1.5 BV/h。纯化后的花生壳总黄酮和木犀草素的纯度分别为10.54%和5.85%，提高了90%和120%。     

不同种源多穗柯主要生物活性成分与矿质元素含量变异分析

【目的】阐明多穗柯主要药用活性成分与矿质元素的种源遗传变异规律。【方法】对设置在江西省分宜县多穗柯全分布区的5个种源试验林植株叶部根皮苷、三叶苷、总黄酮、有机碳、氮、磷和钾元素含量进行测定、分析。【结果】不同种源多穗柯叶部根皮苷、三叶苷、总黄酮、有机碳、全氮、全磷含量差异均存在极显著差异(P <0.01)。不同种源根皮苷含量变异范围为16.03~64.35 mg·g-1,三叶苷含量变异范围分别为4.76~29.97 mg·g-1,根皮苷含量变异范围为61.59~81.05 mg·g-1,其中重庆北碚为根皮苷、有机碳、全磷和全氮含量高的种源,与其他种源相比根皮苷含量最高,四川米易三叶苷含量最高,江西分宜总黄酮含量最高。多穗柯根皮苷含量随日照时数增加呈显著降低趋势(P <0.05),三叶苷含量随无霜期增加呈显著降低趋势,总黄酮含量随经度增加呈极显著增加的趋势,随降水量增加呈显著增加的趋势;根皮苷与全氮含量呈极显著正相关关系,有机碳与全钾含量呈显著负相关关系;聚类分析表明,5个多穗柯种源可划分为2个类群,高根皮苷、高总黄酮、低三叶苷类群和低根皮苷、低总黄酮和高三叶苷类群。【结论】多穗柯根皮苷、三叶苷、总黄酮和主要矿质元素含量具明显种源变异,重庆北碚、四川米易和江西分宜的多穗柯为优良种源。     

大豆质核互作雄性不育系NJCMS1A与其保持系NJCMS1B的生理生化特性比较分析

以大豆质核互作雄性不育系NJCMS1A及其保持系NJCMS1B的花芽为试验材料,利用试剂盒法和紫外分光光度计测定分析了糖分含量(可溶性糖和淀粉)和总ATPase、蔗糖磷酸合成酶(SPS)、磷酸烯醇式丙酮酸羧激酶(PEPCK)、抗坏血酸氧化酶(AO)、过氧化氢酶(CAT)、超氧化物歧化酶(SOD)以及过氧化物酶(POD)等酶活性的变化情况。结果表明:相较于保持系NJCMS1B,总ATPase、PEPCK、AO和CAT活性在不育系NJCMS1A中显著下降;糖分含量、SPS和SOD活性在不育系NJCMS1A中下降水平不显著;POD活性在不育系NJCMS1A中显著上升。根据结果分析推测,与能量代谢或胁迫响应等相关的物质或酶活性在不育系NJCMS1A中的亏损现象可能是NJCMS1A花粉败育的主要原因。     

Polygalacturonase and β-galactosidase activities in Hayward kiwifruit as affected by light exposure,maturity stage and storage time

Softening process and total antioxidant activity were evaluated in kiwifruit differently exposed to light intensity and harvested at two different times (October 10 and November 14). Fruit was stored for 2 months at 0 °C (S1) and then maintained for a week at ambient temperature (S2). The results showed that fruit harvested later presented a faster softening rate during storage than fruit harvested earlier, even if antioxidant activity did not change. Light-exposed fruit showed higher flesh firmness than that of shaded ones. Polygalacturonase activity was higher in kiwifruit maintained for a week at ambient temperature after cool storage and, in particular the highest value was recorded in fruit harvested later. The behaviour of β-galactosidase was different: it did not show changes in fruit harvested later and significantly decreased in light- and shade-exposed fruit harvested earlier.     

家蚕病原性微孢子虫孢子表面蛋白的选择性分离与总蛋白比较分析

选择性分离了Ｎｏｓｅｍａｂｏｍｂｙｃｉｓ孢子表面蛋白和总蛋白，采用ＳＤＳ－ＰＡＧＥ检测发现，孢子表面蛋白由分子量不同的３种亚基（３２０００、２６０００、２４５００Ｄａ）组成，其总蛋白至少包括２５个条带。同时将从养蚕生产中收集到的两种微粒子ＭＡ－１和ＭＤ－１以及从野外昆虫收集到的微孢子虫Ｐｈａ－Ｍ和Ｈａ－Ｍ与Ｎ．ｂｏｍｂｙｃｉｓ进行了比较，发现不同微孢子虫间蛋白组成有差异。     

冷地早熟禾总非结构碳水化合物的季节动态

采用酸提法和水提法两种不同的提取方法对冷地早熟禾的总非结构碳水化合物(TNC)的季节动态进行了研究,同时进行了强度刈割试验以观测TNC与再生的关系。结果显示:冷地早熟禾的TNC季节变化呈宽“U”型,两种提取方法的TNC在返青后都有一个明显的下降过程,酸提TNC在开花期为最低点,水提TNC则是在抽茎期。抽穗期刈割对植株体的再生高度和分蘖数影响最大,而TNC和再生之间并未显示出显著的正相关关系。     

改良热硼酸法高效提取苹果果实RNA

苹果果实、尤其是成熟期的果实中多糖和其他次生物质含量高,难以提取RNA。对此,在原热硼酸法的基础上进行了改进,通过添加提取辅助剂并根据辅助剂特性调整提取步骤,高效、稳定地从苹果果实、尤其是后期果实中提取到了高质量的RNA。所得RNA的A260/A230大于2.0,A260/A280为1.8-2.1,并且RNA产量高,其中前期果实RNA产率在13.40μg/g以上,后期果实RNA产率在7.02μg/g以上,完全可以满足RT-PCR、cDNA-AFLP等分子生物学实验的要求。     

从甜瓜子叶中提取总DNA

用分子标记方法检测甜瓜杂交种子纯度,如果从真叶中提取DNA,检测周期至少需要15d。为了缩短检测周期,我们分别以甜瓜的成熟干种子、吸胀水后“露白”种子、3d龄刚转绿子叶、6d龄子叶、9d龄子叶和12d龄子叶为材料,进行了提取总DNA的研究。结果表明:除了干种子和吸胀水后“露白”种子外,其他的材料都可以提取到DNA,但是DNA的质量因子叶日龄不同而存在很大的差异。不同日龄的子叶中,以3d龄子叶提取的DNA质量好。子叶6d龄时,提取的DNA质量次于3d龄,少量DNA开始出现降解,以后随着子叶日龄的增加,DNA降解加重。另外,与以真叶为材料提取的DNA样品相比较,子叶DNA样品中的蛋白质等杂质含量高,应增加氯仿抽提纯化次数。     

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.