Suitability of Nettle Fiber for Textile Production

IntroductionNettle is a perennial root herd plant of Urticaceaefamily . There are 16 species of Urtica growing in China and6 of them growing in the Northen and Southwesten Chineseprovinces of Xinjiang , Gansu,Sichuan and Shaanxi . Alsointhe Northeast of China nettle abounds as a wild naturalresource . The basts of many Urtica plants stems are rich infibers , which are snowwhite , soft and can be used as atextile materials . The natural harl goods have many specialcharacteristics ,for ins…     

甘蓝型杂交油菜"蜀杂9号"种子纯度的RAPD鉴定

通过50个随机引物对“蜀杂9号”亲本进行RAPD扩增,选出了两个能在父、母本间产生多态性扩增的随机引物S18和S31,在杂种F,代中验证了它们的特异性和稳定性,证明随机引物S18和S31能分别在F1代中稳定扩增出父本和母本的特异标记片段S18750与S31550．对该引物的RAPD-PCR的反应体系优化后,对“蜀杂9号”父、母本和杂种F1代的单株进行了随机检测,结果表明这两个RAPD标记配合使用能稳定可靠地鉴定甘蓝型杂交油菜“蜀杂9号”种子的纯度．     

Expression of lysine-rich protein gene and analysis of lysine content in transgenic wheat

Expression vector pBPC102, which carries winged bean lysine-rich protein (wblrp) gene and dihydropicolinate synthase (DHDPS) gene, was transferred into hexaploid winter wheat cv. Jinghua No.l, Jing411, You899 and Yangnongl5 explants of immature inflorescence and immature embryos by particle bombardment. More than 100 transgenic plants were obtained under the selection of s-(2-aminoethyl)-L-cysteine (AEC). Confirmed transgenic plants of To and TI generation by PCR and PCR-Southern blotting analyses showed successful integration of wblrp gene into wheat genome. Analysis of transgenic plant lines of T2 by Northern dot-blotting showed good expression of wblrp gene in offspring seed. The content of free lysine in leaves, contents of bound lysine and total proteins in seeds of T2 transgenie wheat lines were determined and analyzed. Among 34 tested transgenic lines, levels of free lysine content in leaves of 9 transgenic lines are 2~3times higher than un-trans-formed wild-type cultivars. Among 17 analyzed transgenic lines, bound lysine content of 4 transgenic lines is more than 10% higher than that of wild-type cultivars. Our research suggests that introducing wblrp gene into wheat is an effective way to improve its nutrition quality.     

Involvement of nitric oxide in the signal transduction of salicylic acid regulating stomatal movement

The effects and the relationship between sali-cylic acid(SA)and nitric oxide(NO) on Vicia faba L.stomatal movement were studied.The results here showed that exogenous SA and NO induced stomatal closure,100μmol/L SA induced a rapid and striking NO increase in the cytosol of guard cells.This phenomenon was largely prevented by 2000μmol/L 2-phenyl-4,4,5,5-tetramethylimidazoline-l-oxyl-3-oxide(PTIO),a specific NO scavenger,and 25μmol/L N^G-nitro-L-Arg-methyl eater (L-NAME),an inhibitor of NO synthase(NOS) in mammalian cells that also inhibits plant NOS.In addition,SA-induced stomatal closure was largely prevented by PTIO and L-NAME.These results provide evidence that guard cells generate NO in response to SA via NOS-like activity,and that such NO production is required for full stomatal closure in response to SA.H-(1,2,4)-oxadiazole-[4,3-α]quinoxalin-l-one(ODQ),an inhibitor of guanylate cyclase,and nicotinamide,an antagonist of cADPR production,inhibited the effects of SA-and NO-induced stomatal closure.It suggests that both cGMP and cADPR might mediate the signal transduction of SA and NO-induced stomatal closure.     

Cloning and expressional analyses of a cinnamoyl CoA reductase cDNA from rice seedlings

Cinnamoyl CoA reductase (CCR: EC 1.2.1.44),the entry-point enzyme of the llgnin specific biosynthetic pathway, catalyzes the conversion of cinnamoyl CoA esters to their corresponding dnnamaldehydes. Multiple sequence alignment showed that the deduced polypeptide shared 70% similarity and 30% sequence identity at the amino acid level with defined CCR genes from other plant species and they all contain the common signature sequences thought to be the catalytic site as well as the putative NADP binding domain.Using a conserved OsCCR cDNA fragment as the probe for library screening, we isolated the genomic DNA that covered the whole coding region of OsCCR with total length of 3045bp including 4 introns and 5 exons. The open reading frame for our OsCCR gene coBtAin~ 337 amino adds. Northern blot indicated that OsCCR was expressed in different organs with the highest level found in stems. In situ hybridization results showed that OsCCR mRNA was localized mainly along the vascular bundles in stems and leaves, and also in lateral roots that was differentiating from the tiilering node. We conclude that the vascular-localized expression of OsCCR gene may suggest its possible involvement in llgnin biosynthesis. Cloning and characterization of OsCCR will help to clarify how llgniflcations in plants are regulated and will provide a physical basis for creating genetically engineered rice plants with optimal lignin contents.     

L波段FH频率合成器的设计与实现

设计具有快速频率捷变与低相位噪声性能的Ｌ波段ＦＨ频率合成器,利用ＤＡＣ电路对ＶＣＯ控制电压进行快速预置,大大缩短了频率捷变时间,优选环路分频比Ｎ值和参考分频比Ｒ值,使输出频率与Ｎ值呈非线性关系,即采用非等间隔频方式,有效降低了因环路分频分Ｎ过大的输出相位噪声,当参考源使用普通晶体时,测量结构表明：频率捷变时间〈１０μｓ,输出单边带相位噪声谱密度约为－７０ｄＢ／Ｈｚ（偏离载频１ｋＨｚ）。     

6种凤仙花属(Impatiens L.)植物叶表皮特征的微形态学研究

应用扫描电子显微镜技术首次研究了6种凤仙花属(Impatiens L.)植物的叶表皮微形态学特征,结果表明:6种凤仙花属植物叶片上表皮纹饰为网状、不规则细波状或曲叉状,其中曲叉状纹饰为一种较特殊的纹饰特征;气孔仅分布在叶片的下表面,呈不规则排列,形状为椭圆形或宽椭圆形,长度在10.5-25.6μm之间,气孔外拱盖内缘平滑或近平滑,多数种类气孔的保卫细胞两极具“T”型加厚.叶表面纹饰,气孔的形状、大小及气孔保卫细胞两极“T”型加厚等特征在种间具有一定的差异,可作为该属植物分类的重要特征之一.文中还探讨了叶表皮微形态学特征在凤仙花属分类中的意义及有关紫花黄金凤的分类学地位问题.     

推广的Dirichlet L-函数的加权均值公式

利用Gauss和的定义、三角和估计、特征和的性质及其解析方法讨论了Dirichiet L-函数的2k次加权均值分布问题，得到一个有趣的加权均值分布公式。     

芦荟超氧化物歧化酶(SOD)的分离纯化研究

采用硫酸铵分级沉淀、Sephadex G-100凝胶层析和DEAE-52柱层析,分离纯化了芦荟(A.vera L.)超氧化物歧化酶,纯化倍数为56倍,回收率为54%,比活力为643(U/mgpro),酶的最适pH值为8.2,最适温度在40~55℃,KCN和H2O2能抑制酶活性。实验表明:芦荟中的SOD属Cu、Zn-SOD。