您的位置: 专家智库 > >

国家高技术研究发展计划(2003AA207130)

作品数:8 被引量:94H指数:5
相关作者:郜刚段江燕屈冬玉金黎平雷剑更多>>
相关机构:山西师范大学中国农业科学院蔬菜花卉研究所教育部更多>>
发文基金:国家高技术研究发展计划山西省自然科学基金国家自然科学基金更多>>
相关领域:农业科学生物学更多>>

文献类型

  • 8篇期刊文章
  • 1篇会议论文

领域

  • 7篇农业科学
  • 2篇生物学

主题

  • 6篇马铃薯
  • 4篇青枯
  • 4篇青枯病
  • 4篇枯病
  • 3篇抗性
  • 2篇青枯病抗性
  • 2篇POTATO
  • 2篇病抗
  • 1篇胆碱
  • 1篇胆碱酯酶活性
  • 1篇蛋白
  • 1篇蛋白质
  • 1篇电化学
  • 1篇电化学分析
  • 1篇多酚
  • 1篇多酚氧化
  • 1篇多酚氧化酶
  • 1篇乙酰
  • 1篇乙酰胆碱
  • 1篇乙酰胆碱酯

机构

  • 4篇山西师范大学
  • 2篇教育部
  • 2篇中国农业科学...
  • 1篇国家蔬菜改良...

作者

  • 3篇段江燕
  • 3篇郜刚
  • 2篇金黎平
  • 2篇屈冬玉
  • 2篇柳俊
  • 2篇谢从华
  • 1篇连勇
  • 1篇谢开云
  • 1篇蔡兴奎
  • 1篇安建梅
  • 1篇李林章
  • 1篇闫桂琴
  • 1篇雷剑
  • 1篇李林章
  • 1篇张晓燕
  • 1篇任彩虹

传媒

  • 2篇中国马铃薯
  • 2篇西北植物学报
  • 2篇Agricu...
  • 1篇作物学报
  • 1篇农业与技术
  • 1篇2005年全...

年份

  • 1篇2011
  • 4篇2008
  • 1篇2006
  • 3篇2005
8 条 记 录,以下是 1-9
排序方式:
马铃薯非特异性脂质转移蛋白基因StLTPa1的克隆和表达被引量:12
2008年
非特异性脂质转移蛋白(nsLTP)是植物中大量存在的小分子脂类结合蛋白,具有多种生物学功能,如抗菌防御、信号传导、胞壁松弛、蛋白酶抑制等。通过接种青枯菌(Ralstonia solanacearum),从马铃薯栽培品种中薯3号中获得一个新的非特异性脂质转移蛋白cDNA克隆StLTPa1,序列分析表明该基因含636bp核苷酸,编码91个氨基酸,属于I类非特异性脂质转移蛋白。基于氨基酸序列构建的系统发生树揭示,该基因与其他茄科nsLTP具有高度保守的序列相似性,核酸和氨基酸水平分别具75%~85%和60%~92%的同源性。对该基因在互作早期基因表达时空性分析表明,StLTPa1基因不仅受病菌的诱导,在不同抗、感病的马铃薯基因型中差异表达,而且受一定浓度外源非生物激发子如水杨酸、茉莉酸和脱落酸的诱导并产生一定时间的持续效应,其诱导表达模式也表现出一定的差异。原位杂交结果显示StLTPa1主要在马铃薯茎、叶维管束系统的韧皮部细胞中表达。这些结果说明StLTPa1基因受病菌和非生物激发子诱导,在植物防御反应中发挥作用。
郜刚任彩虹金黎平谢开云屈冬玉
关键词:马铃薯非特异性脂质转移蛋白克隆
马铃薯体细胞杂种的青枯病抗性鉴定被引量:5
2005年
本试验对马铃薯四倍体栽培种(Solanum tuberosum)的双单倍体系81-15与二倍体野生种S.cha-coense的原生质体融合株系进行了青枯病抗性鉴定,其目的是对利用体细胞融合技术获得抗青枯病种质的有效性及抗性鉴定技术进行评价,获得抗病育种材料。结果表明:在鉴定的18个体细胞融合株系中,抗性分离表现为从感病(S)到抗病(R),多数表现为中感(MS)到中抗(MR)水平。田间病圃鉴定、人工接种鉴定和分子标记鉴定的结果显示:田间病圃鉴定的病情指数(DI)和人工接种鉴定病级(DS)的相关性达到极显著水平(DI=-0.39+4 DS,r2=0.921),双侧翼SCAR标记SCA07446和SCA12980鉴定同时具有两个标记特异带的株系均为前两种鉴定表现为中感(MS)以上的材料。综合分析同时利用3种方法鉴定的结果:CHT-3、CHT-5、CHT-6、CHT-10、CHT-15等5个株系为抗病材料,证明体细胞融合是利用野生种质资源抗性的有效途径。
李映蔡兴奎李林章谢从华
关键词:马铃薯体细胞杂种青枯病抗性鉴定
Differential Space-Time Expression of StLTPbl Gene Between Resistant and Susceptible Potato Genotypes in Response to Ralstonia solanacearum
2008年
This study is to investigate the role of lipid transfer protein (LTP1) gene of potato (Solanum tuberosum) in bacterial wilt (Ralstonia solanacearum) resistance. A novel cDNA clone encoding nsLTP was isolated from cultivated potato (Solanum tuberosum) infected with R. solanacearum by 5'-rapid amplification of cDNA ends (RACE). The temporal and spatial expression of StLTPbl was studied during the early stages of potato-R, solanacearum interaction by reverse transcriptase PCR (RT-PCR) and Northern blotting. The sequence analysis of the cloned cDNA, named StLTPbl, showed 691 bp which encoded a type 1 nsLTP of 91 amino acids. Construction of a phylogenic tree showed that StLTPbl is well conserved in the coding region with high identity at the amino acid level with other Solanaceae nsLTPs. The temporal and spatial expression of StLTPbl was studied during the early stages of potato-R, solanacearum interaction. StLTPbl transcription is induced faster and transcripts accumulate to higher concentrations in resistant compared with susceptible genotypes by the pathogen. Dominant differences in the pathogen-induced gene expression pattern between the upper and lower leaves and stems were observed within the same genotypes. In situ hybridization results showed that the StLTPbl mRNA was localized in phloem cells of vascular tissues in potato leaf and stem tissues after pathogen infection. Salicylic acid, methyl jasmonate and abscisic acid could induce StLTPbl gene expression without significant difference between the upper and lower tissues. These abiotic elicitors could produce a long-lastingeffect on the StLTPbl during early stages of potato-R, solanacearum interaction. Differential expression of StLTPbl gene between resistance and susceptible potato genotypes in response to R. solanacearum suggests that this gene plays a key role in plant defense mechanisms.
GAO GangJIN Li-pingXIE Kai-yunQU Dong-yu
关键词:NSLTP
DNA分子标记在马铃薯遗传改良中的应用
随着分子标记技术的不断发展,它已成为一种常规的工具渗透到生物学研究的各个领域,对于作物遗传育种实践更是产生了巨大影响。本文就分子标记在目前马铃薯遗传育种中的种种应用,包括遗传连锁图谱构建,分子标记辅助选择,QTL分析,图...
李林章柳俊谢从华
关键词:马铃薯分子标记
文献传递
Population Improvement of Resistance to Late Blight in Tetraploid Potato:A Case Study in Combination with AFLP Marker Assisted Background Selection
2011年
Cultivated potato with high level of horizontal resistance against late blight is one of the most important goals of potato breeding.The recurrent selection has been adopted to increase the level of potato horizontal resistance and a B3C1 population without R1-R11 dominant genes has been released by the International Potato Center at the short-day condition of Peru.The present research was carried out to further improve the resistance and the agronomic traits of B3C1 population under long-day condition of Hubei,China,with maximized retention of its genetic diversity.Twenty-seven individual clones of B3C1 were used to generate population B3C2 by in-population crossing with the bulk pollens aiming to elevate the frequency of late blight resistance genotypes and to improve the adaptation to local long-day conditions.The late blight resistance and the main agronomic traits including the maturity,the plant characters and the tuber traits were evaluated for the foreground selection in three years,by which 130 pedigrees were maintained as the basic population of B3C2 for further selection.A total of 312 polymorphic loci detected by 9 AFLP marker combinations were used to monitor the genetic diversity of the populations for the background selection.The B3C2 population of 51 clones was finally selected,of which the frequency of resistant genotypes increased by 23.8% points and the genetic diversity was maintained by about 96% as referred to B3C1.Our results strongly suggested that combination of the foreground selection for target traits and the background selection for the genetic diversity is an efficient strategy in the recurrent selection of tetraploid potato to improve quantitative traits.
YAO Chun-guangSONG Bo-taoLIU JunWU Cheng-jinCHENG QunLI Da-chunXIE Cong-hua
关键词:POTATO
番茄碱对乙酰胆碱酯酶活性影响的研究被引量:7
2008年
通过电化学方法分析了番茄碱对乙酰胆碱酯酶活性的影响。结果表明:(1)乙酰胆碱酯酶经盐析、凝胶过滤层析分离纯化,酶比活力达到685.3 U/mg,提纯倍数达到229.5倍;(2)低浓度(1 mmol/L)番茄碱对乙酰胆碱酯酶有明显的激活作用,阳极化扫描的氧化峰电流由1.4μA升至2.8μA;高浓度(10 mmol/L)番茄碱对乙酰胆碱酯酶有明显的抑制作用,阳极化扫描的氧化峰电流由1.4μA降至0.5μA。说明采用循环伏安法、线形扫描电化学手段,对碘化胆碱的电化学行为可分析番茄碱对乙酰胆碱酯酶的活性影响,此项研究为探讨番茄碱的作用机理奠定基础,为研制性能优良的生物传感器提供理论依据。
段江燕张晓燕
关键词:番茄碱乙酰胆碱酯酶电化学分析
马铃薯青枯病抗性的共性AFLP标记的初步定位(英文)被引量:13
2005年
利用集群分类法 bulkedsegregantanalysis,BSA 对与马铃薯青枯病 Ralstoniasolanacearum 抗性连锁的分子标记进行了分析.以马铃薯青枯病高抗性的原始栽培种Solanumphureja获得的二倍体群体为作图群体进行AFLP标记的初步筛选,另选一个与作图群体有较大亲缘关系和相近遗传背景的二倍体群体对所获标记进行验证.在标记鉴定过程中使用了共性AFLP标记 commonAFLPmarker 的方法.通过与已构建的连锁图谱的比较分析,获得了4个与马铃薯青枯病抗性相关的4个AFLP标记ATG/CTC307.0,ATG/CTC246.0,ATG/CTC191.0和AAC/CAC79.0,将其分别定位于染色体1和12上,可望应用于其它相关研究.
郜刚金黎平屈冬玉连勇闫桂琴段江燕
关键词:马铃薯青枯病抗性
一个与马铃薯青枯病抗性连锁的SRAP标记筛选被引量:53
2006年
以两个马铃薯二倍体分离群体ED和CE共105个基因型为材料,利用群分法(BulkedSegregantAnalysis,BSA)筛选与马铃薯青枯病抗性基因连锁的分子标记。在8个正向引物和11个反向引物组成的88对SRAP引物组合中,筛选获得了一个与马铃薯青枯病抗性紧密连锁的SRAP标记M32,遗传连锁分析表明,该标记在ED群体和CE群体中与抗性位点之间的遗传距离分别为10.2cM和17.3cM。
雷剑柳俊
关键词:马铃薯青枯病SRAP标记
感染青枯病马铃薯中几种酶及蛋白质含量变化的研究被引量:5
2008年
〔目的〕揭示感染青枯菌马铃薯抗病机制,推动和指导抗感染青枯菌马铃薯品种的选育。〔方法〕给同一品种的马铃薯接种青枯菌后测定其几种酶的活性及蛋白质含量。〔结果〕接种后苯丙氨酸解氨酶(PAL)活性均比对照高,其中第3天变化幅度较大,约比对照升高4.67倍。接种后PAL的活性变化分别在3天、7天出现2次高峰。过氧化物酶(POD)活性在接种后第5天达高峰,约高于对照3.62倍。多酚氧化酶(PPO)活性在接种后第5天达高峰,第7天达最小值。马铃薯感染青枯病后蛋白质含量呈下降趋势。〔结论〕3种酶活性变化出现的峰值强弱可作为早期鉴定感染青枯菌马铃薯的一种有价值的生理指标。
段江燕安建梅郜刚
关键词:马铃薯青枯病苯丙氨酸解氨酶多酚氧化酶过氧化物酶
共1页<1>
聚类工具0