虾肽有机肥与磷肥配施对苹果产量和品质的影响

[目的]研究虾肽有机肥(SPOF)与磷肥配施的协同增效作用。[方法]采用田间小区试验,设尿素1.4 kg/株(CK)、尿素1.4 kg/株+农家肥50 kg/株+磷酸二氢钾1.54 kg/株(TT1)、尿素1.4 kg/株+SPOF 30 kg/株+磷酸二氢钾1.54 kg/株(TT2)、尿素1.4 kg/株+SPOF 30 kg/株+普通过磷酸钙0.83 kg/株+磷酸二氢钾1.25 kg/株(TT3)。[结果]各处理的产量TT3>TT2>TT1>CK,且TT3达到了显著水平;TT3的品质指标,即可溶性固形物、维生素C、蔗糖、葡萄糖以及硬度均达到了显著水平。[结论]TT3处理虾肽有机肥和磷肥(SSP+KH2PO4)协同将其效力发挥到最大。     

通过GbF3’H基因单独沉默及其与GbCHI和GbDFR基因共沉默研究其在海岛棉中抗枯萎病功能

【目的】通过沉默海岛棉GbF3’H基因及共沉默GbF3’H、GbCHI和Gb DFR基因,研究其在海岛棉抗枯萎病中的作用。【方法】以海岛棉抗病材料06-146为研究对象,GhCLA1基因为阳性对照,空载体为阴性对照,构建海岛棉TRV2-Gb F3’H沉默载体,协同课题组前期构建的TRV2-CHI和TRV2-DFR载体,利用病毒诱导的基因沉默技术(Virus-induced gene silencing,VIGS)分别进行Gb F3’H基因单独沉默以及GbF3’H、GbCHI和Gb DFR这3种基因共沉默试验。通过实时荧光定量聚合酶链式反应(Quantitative real time-polymerase chain reaction,q RT-PCR)分析各处理样品中基因沉默情况;设置室内接种枯萎病菌试验测定病情指数,分析各沉默材料对枯萎病的抗性差异。【结果】q RT-PCR结果显示,海岛棉GbF3’H基因沉默后其在海岛棉根、茎和叶中的表达量比空载体对照低,Gb F3’H、GbCHI和GbDFR这3种基因共沉默后其在海岛棉根、茎和叶中的表达量均比空载体对照低。病情指数调查结果显示,野生型<空载体对照相似文献   

基于多反应监测质谱技术的水稻叶片蛋白绝对定量方法

【目的】建立水稻叶片蛋白的多反应监测(MRM)质谱绝对定量方法。【方法】水稻叶片蛋白经含1.0%十二烷基硫酸钠(SDS)的磷酸盐(PBS)缓冲液提取,丙酮沉淀除杂纯化、胰蛋白酶消化,酶解液经液相色谱分离,MRM质谱监测,外标法定量。【结果】向提取缓冲液中加入1.0%SDS可增强水稻叶片中16种靶蛋白和总蛋白质的提取效果;不同有机试剂处理,总蛋白质沉淀量存在显著差异(P<0.05),沉淀能力从强到弱依次为乙腈>丙酮>异丙醇>甲醇>乙醇;对于16种目标蛋白,总体以丙酮沉淀效果最好,其次是异丙醇和乙腈,甲醇和乙醇效果较差。该方法线性范围均达到3个数量级,定量限为0.1~2.5 nmol/L,灌浆期16种水稻叶片蛋白质含量为6.0~2818.1μg/g,相对标准偏差均小于14%。【结论】SDS可显著提高水稻叶片蛋白提取效果,采用丙酮或乙腈可获得较好的蛋白沉淀效果,但不同蛋白质略有差异。结合MRM质谱监测技术可实现水稻叶片蛋白的绝对定量,方法线性范围宽、敏度高、重复性好。     

二元共沉淀体系去除沼液有机物及机理分析

针对猪场沼液有机质含量高,其他处理工艺周期长、成本高、难去除的问题。采用包含氧化钙水溶液和AlCl3的二元共沉淀体系去除沼液有机污染物。探究了沉淀剂配比、投加量、反应时间、沼液初始pH等因素对有机物去除效果的影响。结果表明:当共沉淀剂体积比为1∶2.5、投加量为1∶1(体积比)、反应时间60 min、pH为9时有机质最大去除率达到93%。通过对反应前后沉淀物XRD、FITR和SEM分析,表明共沉淀剂可与沼液中带负电有机质通过电荷吸引以及与正价金属离子的络合作用絮凝沉淀有机物。沉淀反应迅速且去除有机质较为彻底,在养殖场废水处理中具有良好的工业应用前景。     

Characterization and expression of SLO1 potassium channels during spermatogenesis in Eriocheir sinensis

SLO1 potassium channels are pivotal to many aspects of spermatogenic cell. Experiments were conducted to assess physiology and function of SLO1 potassium channels in different developmental stages of spermatogenic cell in Eriocheir sinensis. First, the expression of SLO1 protein was examined via Western blot, RT‐PCR, immunohistochemistry and immunofluorescence assays. The results showed that the expression of the SLO1 protein was not uniform in the spermatogenic cells of E. sinensis. Second, whole‐cell patch clamp technique was used to record the potassium current of spermatogenic cells and to analyse the electrophysiological characteristics of the potassium channels with the aid of inhibitors. It is proved that the potassium current in E. sinensis germ cells is associated with intracellular Ca²⁺, and the calcium‐activated potassium channel mediated by SLO1 protein is mainly large‐conductance Ca²⁺‐activated K⁺ channels (BK_Ca). Based on these researches, the cDNA of SLO1 from testis was cloned and sequenced. The SLO1 protein contained domains bound to calcium ions, and the spatial structure formed by its tetramers constituted potassium channels. Phylogenetic analysis revealed that SLO1 was much closer to Scylla paramamosain than other examined species. Finally, iberiotoxin (IbTX) and CdCl₂ were used to inhibit the acrosome reaction (AR) induced by A23187 and to explore the role of SLO1 potassium channels in the AR of E. sinensis. The experimental results showed that SLO1 potassium channels were expressed in E. sinensis spermatogenic cells and played an important role in the AR of crab sperm (SP).     

大豆小肽螯合铁的制备工艺及光谱分析研究

通过铁源筛选比较得知,氯化亚铁比较适合与大豆小肽进行螯合反应制备大豆小肽螯合铁,利用响应面法优化了大豆小肽螯合铁的制备工艺,优化结果为:小肽与亚铁盐质量比4∶1,反应pH5.0,反应温度40℃,得到离子螯合率平均值为56.81%,经中试车间生产试制得到大豆小肽螯合铁的得率是78.3%,螯合率为82.39%,检测大豆小肽螯合铁的主要成分中的蛋白含量为78.94%,铁的含量为10.87%。红外和紫外光谱分析检测结果显示:大豆小肽和大豆小肽螯合铁(Fe~(2+))红外吸收峰的强度在不同波长位置上有明显的变化,大豆小肽螯合铁(Fe~(2+))在紫外波长上发生了明显的位移且宽化,表明大豆小肽螯合铁(Fe~(2+))形成了络合物。同时对大豆小肽螯合铁的结构进行了预测。     

接种疫苗的健康风险研究进展

在广泛文献检索的基础上,对疫苗的历史、种类、防腐剂、不良反应和安全接种等进行了综述,为接种疫苗的健康风险研究提供科学资料。     

菜籽油裂解燃料离子液体催化酯化反应降酸工艺的研究

为了降低裂解燃料酸值,增加燃料的稳定性能,将吡啶丁烷磺酸硫酸氢盐应用于菜籽油裂解燃料的酯化反应。考察了催化剂用量、反应时间和反应温度等对酸值的影响,并在最佳优化条件下考察了裂解燃料成品的理化性质。结果表明:吡啶丁烷磺酸硫酸氢盐对催化酯化反应具有很高的催化活性。优化工艺条件为:催化剂用量1.2%、反应温度75℃、反应时间70 min,在此工艺条件下,酸值降低到1.0 mgKOH/g以下。     

Disulphide structure of high-molecular-weight (HMW-) gliadins as affected by terminators

This study aimed at elucidating SS-bonds of HMW-gliadins (HGL) from wheat with the focus on terminators of glutenin polymerisation. HGL from wheat flour extracts non-treated or treated with the S-alkylation reagent N-ethylmaleinimide (NEMI) were compared. HGL from wheat flour Akteur were isolated, hydrolysed with thermolysin and the resulting peptides pre-separated by gel permeation chromatography and analysed by liquid chromatography/mass-spectrometry using alternating electron transfer dissociation/collision-induced dissociation. Altogether, 22 and 28 SS-peptides from samples without and with NEMI treatment, respectively, were identified. Twenty-six peptides included standard SS-bonds of α- and γ-gliadins, high-molecular-weight and low-molecular-weight glutenin subunits. Eleven SS-bonds were identified for the first time. Fifteen peptides unique to HGL contained cysteine residues from gliadins with an odd number of cysteines (ω5-, α- and γ-gliadins). Thus, gliadins with an odd number of cysteines, glutathione and cysteine had acted as terminators of glutenin polymerisation. Decisive differences between samples without and with NEMI treatment were not obvious showing that the termination of polymerisation was already completed in the flour. The two HGL samples, however, were different in the majority of ten peptides that included disulphide-linked low-molecular-weight (LMW) thiols such as glutathione and cysteine with the former being enriched in the non-treated HGL-sample.