外源NO及反向调控PEG胁迫下苜蓿萌发种子抗氧化酶及其同工酶动态的研究

以紫花苜蓿为材料,用一氧化氮供体硝普钠(SNP)及一氧化氮清除剂c-PTIO对苜蓿种子进行浸种处理,采用分光光度法和同工酶电泳技术来研究外源NO及反向调控对PEG胁迫下紫花苜蓿抗氧化酶活性及其同工酶的影响,并探讨NO调控苜蓿种子耐旱性的生理机制。结果表明:PEG胁迫下外施0.1 mmol·L^-1 SNP,第6天时较PEG处理POD活性降低了32.72%;第4天时SOD、CAT活性较PEG处理升高了10.48%、23.60%,有效缓解了PEG对紫花苜蓿萌发中种子的氧化损伤,提高其抗氧化能力。PEG胁迫下添加 c-PTIO抑制了苜蓿萌发期的抗氧化系统活性。从同工酶的谱带数量和强弱来看,POD同工酶各区带活力均随PEG胁迫时间的延长而增加,在第2天酶带只有1条,而第4天酶带呈现9条;SOD和CAT同工酶表达量变化不显著,但酶带强弱有一定变化,S3酶带随处理时间的延长表达量逐渐减弱;CAT同工酶谱带则一直保持2条带,无明显强弱变化。因此,外源NO在PEG胁迫下紫花苜蓿萌发中抗氧化酶快速响应并在维护氧自由基代谢平衡中起重要保护作用。     

两种卵黄抗体不同提取方法的比较试验

卵黄抗体(Ig Y)具有许多其他类型抗体所没有的优点,其分离纯化的方法有有机物抽提法、盐析法、水稀释法等。试验分别用聚乙二醇(PEG)6000和氯仿来提取卵黄抗体,对其收集的抗体量和抗体效价进行比较分析。结果表明:100 g的卵黄用PEG6000法比氯仿法多收集71 m L卵黄抗体溶液,且PEG6000法的成本远远低于氯仿法,有很好的经济效益,而PEG6000法提取的卵黄抗体效价比氯仿法略低一个滴度。     

柱花草叶肉原生质体提取与瞬时表达体系构建

柱花草(Stylosanthes guianensis)是一种重要的热区豆科牧草,为利用原生质体瞬时表达体系开展柱花草基因功能研究,以20 d龄期‘热研5号’柱花草子叶为试验材料,通过正交试验考察不同因素对原生质体分离及转化效率的影响。结果表明：采用1.5%纤维素酶、1.25%离析酶、0.5 mol·L^-1甘露醇和4 mmol·L^-1MES酶解液组合,酶解时间为16 h时,原生质体的产量和活性均达到最佳,分别为(4.567×10⁶)个·g^-1和92.271%;原生质体浓度为(6×10⁵)个·mL^-1、质粒浓度为0.6μg·μL^-1,PEG-4000浓度为50%、转化时间为5 min时,转化效率最高,可达52.524%。构建了目标蛋白SgRKL1表达载体pA7-BIUTNT::SgRKL1-GFP,利用PEG介导法将其转入柱花草原生质体,激光扫描共聚焦显微镜检测结果显示SgRKL1蛋白定位于细胞膜上,说明所建立的柱花草叶肉原生质体瞬时表...     

PEG处理对柠条种子发芽的影响

通过选用渗透调节剂聚乙二醇(PEG)处理柠条种子,并对柠条种子的发芽情况进行试验研究,结果表明:在水分胁迫条件下,柠条种子萌发存在一定的差异;一定浓度范围内,随着PEG溶液浓度的增强,柠条种子的发芽率提高,发芽速度加快。据文献报道,当PEG处理的强度达到一定水平时,会对种子的萌发产生抑制作用,但本试验还没有得到对柠条种子产生抑制作用的PEG浓度。     

水势胁迫对2种菊科种子萌发影响的研究

以莴苣和野菊花为材料,研究了用不同浓度(0,25,50,75,100,150,200 g/L)聚乙二醇溶液模拟干旱处理对2种菊科种子萌发的影响.结果表明:莴苣种子和野菊花种子在PEG浓度为0～75 g/L时,种子发芽率随着PEG浓度的上升而增大,PEG浓度为75 g/L时,种子的发芽率最高,莴苣和野菊花的发芽率分别为90.76％和84.50％;在PEG浓度为75～200 g/L时,种子发芽率随着PEG浓度的上升而逐渐降低,且浓度为200 g/L时,发芽率最低,分别为32.87％和3.50％.对萌发过程形态观察后发现,莴苣种子和野菊花种子在去离子水中的发芽过程不同,莴苣种子先进行胚根的发育而野菊花种子先进行子叶的发育.莴苣种子在去离子水和高浓度PEG溶液中发芽过程不同,在去离子水中莴苣种子先进行胚根的发育,而在高浓度PEG溶液中莴苣种子先进行子叶的发育,野菊花不具备此特征,表明莴苣种子在胁迫条件下,可进行一种适应性成长.     

PEG对胡萝卜花粉离体萌发的影响

研究了不同分子量的PEG（聚乙二醇）对胡萝卜花粉离体萌发的影响。试验结果表明,不同分子量的PEG对花粉离体萌发率的影响不同,PEG-6000较其他2种分子量的PEG促进花粉萌发的效果要好;3种分子量PEG的最适浓度不尽相同,其中PEG-6000促进胡萝卜花粉萌发的最佳浓度为100 g/L,而PEG-4000和PEG-10000促进胡萝卜花粉萌发的最佳浓度均150 g/L。     

In vitro pollen germination in avocado (Persea americana Mill.): Optimization of the method and effect of temperature

An improved in vitro pollen germination method was developed for avocado (Persea americana Mill.). The effect of different concentrations of sucrose, polyethylene glycol (PEG), Mg and Ca on pollen germination was evaluated in order to determine the optimal pollen germination medium, i.e. that maximizing the percentage of pollen germination and minimizing the percentage of bursted pollen grains. Once the germination medium was optimized we used it to study the effect of temperature on in vitro pollen germination and tube growth in different cultivars from the three botanical varieties of avocado, that differ in their adaptation to environmental conditions. Significant differences in percentage of pollen germination and in pollen tube growth were observed among cultivars. These results could have implications not only for optimizing pollen management in avocado but also to select the best pollinizers for a particular cultivar.     

内生真菌对菊花幼苗干旱胁迫生理的影响

 比较了内生葡萄孢菌（C1）和球毛壳菌（C4）菌株诱导下的菊花苗和对照菊花苗,经30 % PEG6000胁迫不同天数后,叶片超氧化物歧化酶（SOD）、过氧化物酶（POD）、苯丙氨酸解氨酶（PAL）活性,叶片丙二醛（MDA）、可溶性蛋白含量,根系活力,以及胁迫15 d后菊花的总生物量。结果表明：PEG胁迫15 d后,C1、C4处理和对照的生物量分别为4.1、4.4和3.3 g,差异达到显著水平。对照根系活力、PAL活性在胁迫前期迅速变化,接菌处理在胁迫前期均基本稳定,延缓了胁迫反应,但随着胁迫时间的延长,各处理差异不显著; MDA含量接菌处理3 d后达到峰值,随后稳定而对照则继续增加,6 d时达峰值,随后逐渐降低,胁迫后期接菌处理和对照无显著差异;各处理POD活性、可溶性蛋白含量都随着胁迫时间的延长先增加后降低,但各处理之间差异不显著。短期干旱条件下,内生真菌有利于菊花耐旱性的提高。     

Seed germination ofThuja orientalis under PEG osmose treatment

Abstrct Thuja orientalis seeds was treated by different molecular weight, different concentration and different lasting time in the Seedling Laboratory of Northeast Forestry University. The results are as follows:(1) it shows significant promoting effects on the germination viability of seeds by different molecular weight of PEG(-6000, -10000 and -20000), and PEG-10000 is the best. (2)Different effects on germination viability, germination rate and simple vigor index are made by different concentration of the same weight molecular(PEG-10000), the promoting effects are shown when the concentration is below 30%, and from 20% to 30% is the best range, but inhibitions will be shown if the concentration is more than 35%. (3)The most suitable lasting time of osmose treatment of PEG-10000 with 20% concentration is from 2 to 4 days, not more than 6 days, but it will show significant inhibition if the treated time is more than 8 days. (4)The treatments of PEG-10000 and PEG-20000 with higher molecular weight can increase the germination rate and seed vigor, and decrease the electric conductivity of the seed soaking liquid after the natural air-dry treatment. The suitable time of natural air-dry is about 6 to 8 hours. It is also concluded that the PEG osmose treatment is an effective method to increase the germination rate by the field simulation in the laboratroy.