GAPB基因原核表达载体的构建

以拟南芥cDNA为模板,用PCR扩增出GAPB的基因全长,然后将GAPB基因片段连接到PET28a（＋）载体上,构建重组质粒并转化大肠杆菌DH5α,经菌落PCR和酶切鉴定筛选出阳性克隆,测序正确后,再将阳性克隆的质粒转化大肠杆菌BL21（DE3）。结果表明：成功构建了原核表达载体PET28a（＋）-GAPB,为后续的G...     

Probing mode of action in plant cell cycle by the herbicide endothall, a protein phosphatase inhibitor

The mode of action of endothall, an herbicide which was reported to inhibit plant protein phosphatases 1 (PP1) and 2A (PP2A), was investigated. For initial characterization, a series of bioassays was used for comprehensive physiological profiling of endothall effects which suggested a phytotoxic mode of action similar to mitotic disrupter herbicides. Unlike known microtubule disrupters, endothall did not inhibit soybean tubulin polymerization in vitro. As shown in meristematic corn root tips, endothall distorted the orientation of cell division plane and microtubule spindle structures which led to cell cycle arrest in prometaphase. In tobacco BY-2 cells, malformed spindles together with prometaphase arrest of nuclei and abnormal perinuclear microtubule patterns were detected as early as 4 h of endothall treatment. These effects were also observed after treatment with other protein phosphatase inhibitors, cantharidin and okadaic acid, which phenocopied the mitotic changes described in tonneau1 (ton1) and tonneau2 (ton2) Arabidopsis mutants. These mutants are defective in TONNEAU2 (TON2) protein, a regulatory subunit of PP2A, which governs cell division plane and microtubule orientation. Therefore, PP2A/TON2 phosphatase complex is suggested to be an in planta molecular target of endothall. However, in BY-2 cells, additional effects of endothall, including inhibition of S-phase initiation and DNA synthesis, detected by 5-ethynyl-2′-deoxyuridine (EdU) incorporation, and condensed nuclei arrested in late mitosis were observed which were not reported in Arabidopsiston1 and ton2 mutants. This result indicates that two additional checkpoints in cell cycle were blocked by endothall which are probably not associated with TON2-pathway inhibition. Possibly, inhibition of PP1 and/or other PP2A protein phosphatases are involved in the regulation of these cell cycle phenomena.     

新疆南部棉区转Bt基因棉花Bt杀虫蛋白表达规律研究

为研究新疆南部植棉区转Bt基因棉花Bt杀虫蛋白时空表达规律,本文利用ELISA技术于2009年和2010年对南疆种植的转Bt基因棉花‘中棉所41’、‘中棉所43’、‘236’、‘K9030’、‘T3’、‘中棉所44’、‘中棉所45’、‘K7’和‘SGK321’各生育期中不同器官中的Bt杀虫蛋白含量进行测定。结果发现：在时间表达上,大多数转Bt基因棉花叶片的Bt杀虫蛋白含量随着棉花发育进程而逐渐下降,在子叶期含量最高,至蕾期或吐絮期达到最低点。并且不同品种间Bt杀虫蛋白含量差异显著。在空间表达上,在花铃期,棉铃和花苞叶的Bt杀虫蛋白含量最低,大多数品种表现为叶片＞棉蕾＞花瓣（花柱）＞棉铃和花苞叶。     

类钙粘蛋白对Cry3A毒素杀虫活性的影响

将克隆的黄粉虫类钙粘蛋白基因片段在大肠杆菌中表达纯化,并分析其对Cry3A毒素杀虫活性的影响,从而探讨黄粉虫类钙粘蛋白对Cry3A毒素杀虫活性的增效作用。黄粉虫类钙粘蛋白基因片段在大肠杆菌中表达产物为包涵体,经尿素变性后,用亲和纯化法可得到较纯的重组蛋白;随着类钙粘蛋白片段与Cry3A质量比值的升高,Cry3A毒素对黄粉虫的杀虫活性也逐步提高,当其比值为1时,活性达到最大,提高了2.5倍,而黄粉虫类钙粘蛋白片段对Cry3Am的杀虫活性却没有显著性影响。研究表明,黄粉虫类钙粘蛋白对Cry3A毒素的杀虫活性具有增效作用。     

生防菌哈茨木霉FJAT-9040的GFP标记及土壤定殖示踪

哈茨木霉Trichoderma harzianum FJAT-9040对茄科尖孢镰刀菌具有较强拮抗作用。为跟踪分析该菌株在土壤中的存活与定殖特性,利用PEG-CaCl2介导的原生质体转化体系,筛选获得1株荧光性状稳定的菌株FJAT-9295,该菌株在生长速率、产孢量、对酸碱度和温度的适应性及对尖孢镰刀菌的抑菌活性等方面与野生型菌株FJAT-9040无显著差异（P〉0.05）。同时,研究了菌株FJAT-9295在4种类型土壤中的定殖能力以及作物生长对该菌株在土壤中定殖的影响。结果表明：菌株在育苗土中定殖最好,其次为沙土及菜园土,黄泥土中定殖最差;种植茄子比未种植作物的土壤更有利于菌株的存活;菌株FJAT-9295在不同类型土壤中的菌落数随时间的延长均略有下降,16天后趋于稳定,维持在105 CFU/g,较初始接菌量下降了约1个数量级。     

茶树叶片内核酮糖二磷酸羧化酶酶蛋白水平的研究

茶树叶片内核酮糖二磷酸羧化酶蛋白水平,随着新梢叶片的逐渐成熟而增加,当叶龄在33～48天,叶片完全成熟时,蛋白水平达最高值并持续稳定,以后随叶龄的进一步增大而呈下降趋势;叶位试验也表现出相同的变化规律,以芽下第4～6叶位叶中的蛋白水平为稳定最高;在年生育过程中,不同品种春梢叶在春、夏、秋三季中的蛋白水平均以夏季最低,但福鼎大白茶表现为春>秋,而龙井43与龙井长叶表现为秋>春;不同品种春、夏、秋三季新梢叶中的核酮糖二磷酸羧化酶蛋白水平差异,福鼎大白茶与政和大白茶表现为春>秋>夏的规律,龙井43、龙井长叶、迎霜、水古四品种则以秋季最高,春、夏差异不大.     

嫁接黄瓜的光合特性及叶片激素含量和可溶性蛋白研究

以黑籽南瓜为砧木，以津绿21-1和津研4号2个黄瓜品种为接穗，对嫁接植株的光合指标及叶片激素含量和可溶性蛋白进行对比研究。结果表明，2个品种嫁接植株的净光合速率(Pn)、气孔导度(Gg)和胞间C02浓度(Ci)均极显高于自根植株；嫁接植株叶片GA和ABA含量也与自根植株存在显差异，嫁接植株叶片ABA／GA值在测定的各个时期均显高于自根植株；通过等电聚焦聚丙烯酰胺双向电泳(IEF-SDS：PAGE)对叶片可溶性蛋白进行分析对比，发现在嫁接植株叶片中产生了1～2种特异蛋白。     

热研2号柱花草干燥特性及粗蛋白质变化的试验研究

以热研2号柱花草为研究对象，采用快速薄层干燥的试验方法，研究干燥过程中表现出来的干燥特性及不同干燥时间和时期粗蛋白质的变化关系。确定干燥速度与干燥介质温度、含水率与干燥时间、粗蛋白质损失率与干燥介质温度之间的变化方程，分析了各参数之间的关系。结果表明：鲜草刈割后，必须在8 h内进行快速干燥；快速干燥的适宜温度为140～180℃。     

春石斛兰类原球茎分化过程中抗氧化酶活性和可溶性蛋白的变化

以春石斛兰(Dendrobium nobileSw.)为试材,研究了类原球茎在分化芽和根系发生过程中抗氧化酶系统中多种酶活性及可溶性蛋白的变化规律。结果表明,在分化过程中抗坏血酸过氧化物酶(APX)、愈创木酚过氧化物酶(POD)、多酚氧化酶(PPO)和过氧化氢酶(CAT)的活性和可溶性蛋白含量均呈现先降后升的趋势;超氧化物歧化酶(SOD)活性则呈现先升后降的变化。对过氧化物酶同工酶和可溶性蛋白进行SDS-PAGE电泳发现,在分化过程中均有新谱带的产生或原有谱带的消失。