苏云金芽胞杆菌JQD117菌株对韭蛆体内几种酶活性的影响

为明确苏云金芽胞杆菌JQD117对韭蛆幼虫蛋白酶和解毒酶活性的影响，测定比较了感染Bt后幼虫体内胰蛋白酶、胰凝乳蛋白酶、乙酰胆碱酯酶、谷胱甘肽-S-转移酶和羧酸酯酶的活性。首先采用室内生物活性测定方法明确了菌株JQD117对韭蛆3龄幼虫72 h的LC₅₀为2.8070×10⁷cfu/mL，然后采用10×LC₅₀、1×LC₅₀和0.1×LC₅₀三个浓度饲喂感染韭蛆幼虫，定期取样测定韭蛆体内5种酶活性，结果表明以较高浓度（1×LC₅₀和10×LC₅₀）感染韭蛆幼虫后体内蛋白酶和解毒酶活性变化较大，而以低浓度（0.1×LC₅₀）感染韭蛆幼虫后体内蛋白酶活性变化较小。其中，以1×LC₅₀和10×LC₅₀浓度感染韭蛆幼虫后，胰蛋白酶和乙酰胆碱酯酶活性在24~36 h和6~60 h与对照相比均显著升高；类胰凝乳蛋白酶和羧酸酯酶活性在6~60 h与对照相比均受到显著抑制。以0.1×LC₅₀浓度感染韭蛆幼虫后，胰蛋白酶活性只在36 h时与对照相比显著升高；乙酰胆碱酯酶活性在12~48 h时与对照相比显著升高；羧酸酯酶活性只在6 h与对照相比受到显著抑制；类胰凝乳蛋白酶活性与对照相比均无显著变化。谷胱甘肽-S-转移酶活性在三种感染浓度下与对照相比均无显著变化。可见，感染JQD117对韭蛆体内蛋白酶和解毒酶活性均产生了不同程度的影响，且随感染浓度的升高而增强，扰乱了韭蛆正常的生理代谢和对外源毒素的分解，本文为Bt防治韭蛆应用和开发提供了理论指导。     

一株盐芽孢杆菌的筛选及其粗酶的酶学特性研究

从浙江舟山市双峰盐场中筛选出一株分泌蛋白酶的嗜盐菌,结合16S rDNA基因序列鉴定、菌株形貌特征确定其为特氏盐芽孢杆菌(Halobacillustrueperi)命名为HalobacillustrueperiB1。经研究,该菌株最适生长NaCl浓度为5%,表明其为中度嗜盐菌。该蛋白酶在50℃和pH 7.5条件下具有最高的蛋白酶活力。对发酵培养时间的优化实验表明发酵8 h后B1分泌的蛋白酶活力最大。对发酵培养基的优化结果表明,脱脂奶粉为最适氮源和碳源;75 g·L~(-1)为最佳发酵盐浓度,对钙镁离子的依赖不明显。确定优化后的发酵培养基:Na HCO_30.06 g,KCl_2.0g,CaCl_2·2H_2O0.48 g,Mg SO_4·7H_2O 1.0 g,FeCl_3 0.001 g,NaCl 75.0 g,脱脂奶粉10.0 g。在初始pH 7.5,温度为40℃条件下发酵8 h。     

芒果中性/碱性转化酶MiNI基因的克隆与表达分析

采用RT-PCR技术克隆了1个编码NI基因的cDNA序列,命名为MiNI基因,并对不同来源的中性/碱性转化酶的分子特征及系统进化进行比较分析。结果表明：MiNI基因开放阅读框为2034 bp,编码677个氨基酸,相对分子量为76.6 kDa,理论等电点为6.24;生物信息学分析结果显示,NI二级结构α螺旋占38.85%,无规则卷曲占35.45%,伸展链占18.91%,β折叠占6.79%;MiNI具有glycoside hydrolase family 100结构保守域,与克里曼丁桔、龙眼、巴西橡胶树和番木瓜都具有一致的motif位点;MiNI基因编码的氨基酸序列与克里曼丁桔、龙眼氨基酸序列同源性最高;构建NI系统进化树分析表明,与芒果遗传距离最近的是克里曼丁桔,最远的是玉米和枸杞。qRT-PCR分析显示,果皮MiNI基因表达量远高于果肉;花后10~40 d,果皮MiNI基因表达量显著下降;花后40~100 d,果皮MiNI基因表达量维持在一个相对稳定水平;花后100~130 d,随着果实成熟,果皮MiNI基因表达量又显著上升;而花后10~40 d,果肉MiNI基因表达量显著下降,至果实发育后期果肉MiNI基因表达量始终处于极低水平。该研究为进一步了解MiNI基因在芒果果实蔗糖代谢过程中的作用以及从分子角度阐明芒果糖代谢机理奠定理论和技术基础。     

Using vibrational molecular spectroscopy to detect moist heating induced carbohydrates structure changes in cool-climate adapted barley grain

There is limited research to study how moist heating affects internal structure of barley grain on a molecular basis. The objectives of this study were to use vibrational molecular spectroscopy: 1) to determine the moist heating induced changes of barley carbohydrate (CHO) structure on a molecular basis, 2) to study the effects of moist heating on CHO chemical profiles, Cornell Net Carbohydrate and Protein System (CNCPS) subfractions, in situ rumen degradation, and predicted intestinal carbohydrate supply of barley grain; and 3) to reveal the association between molecular structure spectral features and CHO related metabolic characteristics. Barley samples (CDC cowboy) were collected from Kernen Crop Research Farm (Saskatoon, Canada) during two consecutive years. Half of each sample was kept as raw barley and the other half underwent moist heating (autoclaving at 120 °C for 60 min). The molecular spectroscopy (attenuated total reflectance-fourier transform infrared, ATR-FTIR) was used to detect the barley CHO related molecular structure spectral features. Moist heating did not affect carbohydrate related chemical profiles and CNCPS subfractions but it decreased rumen degradable carbohydrate. Rumen undegradable and intestinal digestion of CHO subfractions were not affected by moist heating. The advanced vibrational molecular spectroscopy can be used to detect carbohydrate molecular spectral features. Nutrient utilization prediction using molecular spectral characteristics is warranted and further investigation is encouraged.     

Increased abundance of patatins,lipoxygenase and miraculins in a thaxtomin A-habituated potato Russet Burbank somaclone with enhanced resistance to common scab

Potato common scab caused by the actinobacterium Streptomyces scabiei is characterized by the formation of corky lesions on tubers that reduce their marketability. Management of common scab is very complex and often ineffective under various environmental conditions. Using potato varieties that are more resistant to common scab remains one of the most efficient strategies to control this disease. However, very little is known about the factors associated with resistance to common scab. Somaclone RB9 regenerated from thaxtomin A-habituated potato Russet Burbank calli produced tubers more resistant to common scab than the original variety. Comparison of the RB9 tuber proteome with that of Russet Burbank using label-free quantitative proteomic analysis revealed changes in the accumulation of defence-related proteins from the patatin and lipoxygenase (LOX) families, which are involved in the metabolism of lipids, and of two miraculins of the Kunitz-type protease inhibitors family. The implication of LOX during common scab infection was studied using synchronized minitubers developed from leaf-bud cuttings. S. scabiei infection stimulated the accumulation of LOX in both Russet Burbank and RB9 minitubers, but this accumulation was intensified in RB9 minitubers. Infection also increased LOX activity in Russet Burbank and RB9 minitubers. However, LOX activity measured in noninfected RB9 minitubers was similar to that of infected Russet Burbank minitubers, indicating endogenous activation of LOX activity in RB9 minitubers. We discuss how increased LOX abundance and activity in the somaclone RB9 may contribute to improving tuber defence against common scab.     

寄生虫半胱氨酸蛋白酶核酸疫苗的研究进展与应用前景

就寄生虫半胱氨酸蛋白酶的一些生理生化与免疫学性质进行了概括,阐述了该酶与宿主免疫应答之间的作用关系,证明了该酶具有作为研制高效核酸疫苗的条件,同时综述了寄生虫半胱氨酸蛋白酶核酸疫苗的发展以及应用前景。     

Evaluation of embryonic age and the effects of different proteases on the isolation and primary culture of chicken intestinal epithelial cells in vitro

The present study evaluates the effects of embryonic age and proteolytic enzymes on the isolation and primary culture of chicken enterocyte and to establish an effective technique for chicken intestinal epithelial cell (IEC) cultivation. Fourteen‐day‐old, 16‐day‐old and 18‐day‐old embryos (average weight: 52.23 ± 0.76 g, 50.86 ± 0.99 g, 48.98 ± 1.03 g) were the source for preparation of enterocyte culture, and trypsin‐ethylene diamine tetraacetic acid, collagenase, thermolysin and combination of collagenase and thermolysin were used for digestion medium. Optimal culture protocols were determined by qualitative assays of proliferation. Cells isolated by using 14‐day‐old embryo and collagenase obtain the best attachment and growth in culture, and the production of continuously growing IEC cultures. Thus, we conclude that the use of collagenase as a dissociating enzyme and 14‐day‐old embryo as a source can be advantageously applied to the isolation of chicken IEC and this method may be useful for various applications and basic studies of the intestinal tract concerning such objects as physiology, immunology and toxicology.     

关于漏电保护器误动作的原因分析

本文以单相漏电保护器为例,阐明其几种错误接线的原因,并针对其不同的错误安装接线方法,提出了具体的改进措施。