外源激素脱落酸对小麦幼苗脯氨酸含量的影响

用外源激素脱落酸处理小麦幼苗,结果发现小麦幼苗体内的脯氨酸含量不仅随着外源脱落酸的浓度增大而增加,而且在处理的48小时内,随处理时间的延长,脯氨酸含量持续增加,处理48小时后,幼苗体内脯氨酸含量开始减少,表明脱落酸能促进脯氨酸的合成,抑制脯氨酸的分解。     

40%野草净水基微乳剂麦田除草试验

田间试验表明，４０％野草净水基微乳剂防除小麦田中野燕麦和阔叶杂草较单用燕麦枯和２，４－Ｄ丁酯不仅效果好，而且省工、省时，在以野燕麦和以阔叶杂草为主的麦田使用剂量分别为１８００ｇ／ｈｍ２和９００～１２００ｇ／ｈｍ２。     

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.     

小麦新品种"54368"生育的农业气象条件试验总结

用鲁麦1号小麦作对照,通过分期播种的方法,对小麦新品种"54368"进行了田间试验.结果显示,54368小麦需要的热量条件少于鲁麦1号,生育期比鲁麦1号短2天左右,抗蚜虫能力比鲁麦1号略差,抗锈病能力与鲁麦1号相当,丰产性能明显优于鲁麦1号.     

cDNA cloning and functional analysis of 4-coumarate --CoA: ligase (4CL) gene in Chinese white aspen

cDNA encoding 4-coumarate: CoA ligase (4CL) was isolated from the secondary developing xylem of Chinese white aspen (Populus tomentosa) by RT-PCR for the first time, which was 1619 bp in length. The coding sequence and putative amino acid sequence showed 97.53% and 97.00% identity to that of Pt4CL1 in quaking aspen (P. tremuloids), respectively. Molecular analysis indicated that 4CL was encoded by multiple genes in P.tomentosa, its mRNA was highly accumulated in xylem and the expression of 4CL revealed a biphasic pattern in one growing season, almost in phase with the expression of other related enzymes in lignin biosynthesis. Transgenic research showed that expression of antisense 4CL cDNA led to the decreasing of lignin content in transgenic tobaccos, among which the average reduction was 10.3% and the highest could be up to 18.9%. These data suggested that 4CL gene was a potential gene used in altering lignin biosynthesis by biotechnology for producing new materials of papermaking.     

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.     

暗管排降对小麦养 分、干物质、籽粒产量及品质的影响

着重探讨了南方不同生态类型圩区农田埋设塑料暗管对小麦地上部分矿质营养吸收、干物质累积和分配、产量及品质的影响。试验结果表明：农田埋设塑料暗管排水能显著提高麦株地上部分对Ｎ、Ｐ,Ｋ矿质营养元素的吸收,促进小麦各生育期尤其是拔节孕穗期地上部分干物质累积,小麦增产幅度达到２０．３％￣５３．３％,并能提高籽粒蛋白质和氨基酸含量,改善小麦籽粒的品质。     

水分胁迫条件下化控物质浸种对小麦根苗生长的影响

采用水培溶液添加PEG6000模拟干旱胁迫的方式，研究了化学调控物质浸种对不同程度水分胁迫下小麦根系及幼苗生长影响。结果表明，水分胁迫不同程度地降低了小麦幼苗的株高、叶面积、地上部及根的干重、根系活力、SOD、POD活性等，并明显增加了根系MDA含量水平。化学调控物质浸种处理可以增加各种条件下小麦的总根长、叶面积、根活力及SOD与POD活性，且表现出在干旱胁迫下增加幅度高于正常处理的现象。化学调控物质浸种有利于缓解干旱胁迫带来的不良影响。利用FA、GA、MET及稀土等化学调控物质浸种具有促进根系生长、培育小麦壮苗的突出作用。图3，表2，参14。     

黑麦KingⅡ中白粉病抗性基因的染色体定位

寻找新的白粉病抗源对促进小麦白粉病抗性育种有重要意义.黑麦是重要的白粉病抗源之一,加强对黑麦白粉病抗性调查的研究也将有利于小麦育种.本实验调查了黑麦KingⅡ及衍生自中国春×黑麦KingⅡ的一套小麦一黑麦附加系的白粉病抗性.结果表明,黑麦KingⅡ对白粉病免疫,附加系中除3R和6R附加系对白粉病表现免疫外,其余5个附加系都高感白粉病.该结果表明3R和6R染色体上的白粉病抗性基因可以在小麦背景中得到表达.这为将黑麦白粉病抗性基因导入小麦提供了直接的桥梁材料.