四种切花保鲜液比较试验

采用4种保鲜液对3种切花材料进行保鲜效果研究,结果表明,3%葡萄糖 150 m g/L 8-羟基喹啉 250 m g/L柠檬酸 25 m g/L水杨酸处理菊花、石竹、栀子花切花,在延长切花的瓶插寿命、增大切花花径、延长切花的观赏期方面的效果好于另外3种保鲜液,即10 m g/L硝酸银,25 m g/L水杨酸及蒸馏水(每天定时加用15%C aC l2喷洒花蕾),但4种保鲜液均对栀子花切花的观赏期无明显影响。     

阜新地区花生地液态膜防风蚀措施研究

阜新地区是我国种植花生的主要示范基地,由于花生收割后,花生地处于裸露状态,地表没有植被覆盖,土壤容易受风力侵蚀使得土壤肥力下降,环境遭破坏。通过对阜新地区花生地液态膜防风蚀试验,结果表明,液态地膜对花生地的防风作用明显,使花生地含水量高于对照。使用液态地膜还利于花生长生,可增加产量。     

压榨对烟草薄片纸基性能的影响

采用造纸法对烟梗和烟末制烟草薄片纸基进行了实验研究,探讨了压榨对烟草薄片纸基性能的影响。结果表明,压榨压力从0 MPa上升至0.4 MPa,薄片纸基的抗张指数由17.27 N.m/g逐渐增加到23.69 N.m/g,撕裂指数由2.00 mN.m2/g下降至1.69 mN.m2/g,松厚度从2.43 cm3/g下降到1.80 cm3/g,紧度由0.41 g/cm3上升0.56 g/cm3,薄片纸基的透气度由1.20μm/(Pa.s)下降到0.04μm/(Pa.s),薄片纸基的填充值由7.23 cm3/g逐渐下降到6.08 cm3/g。随着压榨压力的增加,润湿性Max值(tW,max)和特征值(t95)呈相近变化规律,压榨压力为0 MPa时,tW,max值最小(0.097 s),t95值最小(0.442 s),烟草薄片纸基具有较好的渗透性能和较开放的表面结构。扫描电镜分析结果表明,在低压榨压力(<0.2 MPa)条件下,能够显著提高薄片纸基内部的孔隙率,有利于改善薄片纸基的填充值和透气度,并且可以提高薄片纸基的渗透性能。     

高效液相色谱法测定花生仁中甲咪唑烟酸残留

目前花生仁中甲咪唑烟酸残留量的检测是参考国标中茶叶农残的方法,花生仁基质含有大量的油脂和蛋白质,这与茶叶基质有显著区别,且该方法只能定性。本文建立了一种高效液相色谱法定量检测花生仁中甲咪唑烟酸残留量的方法。花生仁样品采用乙腈溶液提取后再经过除脂净化处理,以乙腈:0.02mol/L磷酸二氢钾缓冲液(加入0.1%的三乙胺,磷酸调pH3.0)体积比1:3作为流动相进行高效液相色谱紫外检测器分析。结果表明:甲咪唑烟酸标准在0~1.2mg/L范围内线性关系良好(R2=0.9999),检出限为7μg/kg;加标回收率为91.1%~98.9%;精密度、重复性、稳定性都较好。该方法操作简便、分离度好、结果准确,能很好地满足花生仁中甲咪唑烟酸残留量检测的要求。     

油菜薹和蕾中硫代葡萄糖苷组分及含量分析

采用超高效液相色谱(UPLC)法,对30个油菜品种薹和蕾中硫代葡萄糖苷(glucosinolate,简称硫苷)的组分及含量进行测定。结果表明:30个油菜品种的总硫苷含量变异范围较大,在21.67～119.29μmol·g^-1之间;大多数油菜品种蕾中的硫苷含量高于薹,蕾中硫苷含量均值为37.26μmol·g^-1,薹中为28.06μmol·g^-1;薹和蕾中的硫苷组分相似,均以4-戊烯基硫苷和2-羟基-3-丁烯基硫苷为主要成分,两者在薹和蕾中的含量分别占总硫苷含量的46.24%、28.52%和45.19%、29.13%。进一步分析高、中、低硫苷含量油菜品种的硫苷组分及含量,结果表明油菜不同品种间硫苷含量的差异主要是由4-戊烯基硫苷引起的。     

Study on Quality Standards of Children Antipyretic Lotion

[Objectives]To establish suitable quality standards of children antipyretic lotion.[Methods]Qualitative identification was performed for Paederia scandens and A...     

香蕉中噻唑膦残留分析方法研究

建立香蕉中噻唑膦的超高效液相色谱串联质谱法(UPLC-MS/MS)残留测定方法。香蕉样品采用乙腈提取和PSA+C18分散固相萃取,采用UPLC-MS/MS多反应模式(MRM)进行分析测定。噻唑膦在添加水平0.01~1.0 mg/kg范围内,平均回收率为94.3%~107.5%,相对标准偏差为7.9%~11.0%。采用外标法定量,方法的检出限为0.001μg/m L,定量限为0.005 mg/kg。该方法简单、准确、重复性较好且节省溶剂,适用于香蕉中噻唑膦的残留检测。     

青霉菌发酵液对大豆幼苗生长及生理特性的影响

采用室内生理检测及生物化学方法,研究了青霉菌发酵液对大豆幼苗生长及生理特性的影响。结果表明:用一定浓度的青霉菌发酵液对大豆浸种和茎叶处理,大豆幼苗的生长呈明显上升趋势,处理后大豆的株高、根长、株鲜重和根鲜重均明显得到了提高,且生长状态好于对照,不同浓度处理间具有明显差异,在发酵液浓度为5 g·L-1时,效果最佳。尤其是对根鲜重的影响,促进率最高可达56.21%,同时增强了幼苗根系活力,最大可以提高57.82%,浸种和茎叶处理后,分别提高了叶绿素含量41.25%和15.40%;超氧化物歧化酶活性12.20%和11.70%;过氧化物酶31.33%和29.95%;过氧化氢酶活性42.8%和20.0%,这为发酵液在大豆田推广应用、提高大豆产量提供了重要理论依据。     

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.     

Polymerisation of gluten proteins in developing wheat grain as affected by desiccation

The breadmaking quality of wheat is affected by the composition of gluten proteins and the polymerisation of subunits that are synthesised and accumulated in developing wheat grain. The biological mechanisms and time course of these events during grain development are documented, but not widely confirmed. Therefore, the aim of this study was to monitor the accumulation of gluten protein subunits and the size distribution of protein aggregates during grain development. The effect of desiccation on the polymerisation of gluten proteins and the functional properties of gluten were also studied. The results showed that the size of glutenin polymers remained consistently low until yellow ripeness (YR), while it increased during grain desiccation after YR. Hence, this polymerisation process was presumed to be initiated by desiccation. A similar polymerisation event was also observed when premature grains were dried artificially. The composition of gluten proteins, the ratios of glutenin to gliadin and high molecular weight-glutenin subunits to low molecular weight-glutenin subunits, in premature grain after artificial desiccation showed close association with the size of glutenin polymers in artificially dried grain. Functional properties of gluten in these samples were also associated with polymer size after artificial desiccation.