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小麦与白粉病菌互作中β-1,3-葡聚糖的细胞定位 被引量:3

Localization of β-1,3-glucan during interaction between wheat and barley and their powdery mildew pathogens
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摘要 利用免疫胶体金方法对小麦与白粉病菌互作过程中 β 1,3 葡聚糖酶底物 ,即β 1,3 葡聚糖的合成与分布情况进行了研究。结果发现 ,白粉病菌的所有器官包括分生孢子、附着胞、入侵栓、吸器和菌丝中均未发现 β 1,3 葡聚糖存在 ;相反 ,β 1,3 葡聚糖是小麦各种细胞壁的正常组分 ,在气孔保卫细胞、纤维细胞、导管分子等的细胞壁中含量非常丰富。病原菌的侵染导致植物细胞中β 1,3 葡聚糖的合成增加 ,但在乳突结构中不含 β 1,3 葡聚糖。以上结果说明 ,往小麦中导入外源 β 1,3 葡聚糖酶基因并高效表达 ,不会对病原菌结构产生直接的破坏和抑制作用 ;相反 。 The synthesis and distribution patterns of β 1,3 glucan during the interaction between wheat and its powdery mildew pathogen were examined with cytochemical method. The results showed that there was no β 1,3 glucan located in any parts of the pathogen, such as conidia, appressoria, penetration pegs, haustoria, and hyphae. In contrast, β 1,3 glucan was found in the host cell walls, especially to be abundant in guard cells of stomas, fibre cells, vessel elements, and epidermal hairs. The pathogen infection could result in the accumulation of β 1,3 glucan in the plant cell walls but not in the papilla formed at the penetration sites. These contradicted the assumption that over expression of β 1,3 glucanase genes in transgenic wheat could enhance plant resistance against powdery mildew by directly digesting the fungal haustoria and hyphae. Instead, it can be supposed that the unsuitable expression would disturb the normal development of plants.
出处 《植物病理学报》 CAS CSCD 北大核心 2003年第3期220-224,共5页 Acta Phytopathologica Sinica
基金 国家自然科学基金资助项目 (39870 50 0 )
关键词 小麦 白粉病菌 Β-1 3-葡聚糖 细胞定位 免疫胶体金方法 分生孢子 附着胞 入侵栓 wheat powdery mildew β 1,3 glucan localization.
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参考文献15

  • 1蓝海燕,张丽华,王兰岚,陈正华,田颖川,陈正华,王长海.表达β-1,3-葡聚糖酶及几丁质酶基因的转基因烟草及其抗真菌病的研究[J].Acta Genetica Sinica,2000,27(1):70-77. 被引量:84
  • 2蓝海燕,王长海,张丽华,刘桂珍,王岚兰,陈正华,田颖川.导入β-1,3-葡聚糖酶及几丁质酶基因的转基因可育油菜及其抗菌核病的研究[J].生物工程学报,2000,16(2):142-146. 被引量:67
  • 3胡东维,李振岐,康振生.小麦抗白粉病菌侵染乳突反应的超微结构研究[J].植物病理学报,1998,28(4):309-316. 被引量:8
  • 4Collinge D B, Kragh K M, Mikkelsen J D, et al. Plant chitinase[J].Plant Cell, 1993, 5(1):31-40.
  • 5Castresana C, de Carvalho F, Gheysen G, et al. Tissue-specific and pathogen-indaced regulation of a Nicotiana plumbaginifolia beta-1, 3-glucanase gene[J]. Plant Cell, 1990, 2(12):1131-43.
  • 6Dixon R A, Lamb C J, Masoud S, et al. Matabolic engineering:prospects for crop improvement through the genetic manipulation of phenylpropanoid biosynthesis and defense responses -- a review [ J ].Gene, 1996, 179(1):61-71.
  • 7Jach G, Cornhardt B, Mundy J, et al. Enhanced quantitative resistance against fungal disease by combinatorial expression of different barley antifungal proteins in transgenic tobacco[J]. Plant J., 1995, 8(1):97- 109.
  • 8Neuhaus J M, Flores S, Keefe D, et al. The functice of vacuolar beta-1,3-glucanase investigated by antisense transformation. Susceptibility of transgenic Nicotiana sylvestris plants to Cercospora nicatianae infection[J]. Plant Mol. Biol., 1992, 19(5):803-813.
  • 9Verma D P, Hong Z. Plant callose synthase complexes[J]. Plant Mol.Biol., 2001, 47(6) : 693 - 701.
  • 10Worrall D, Hird D L, Hodge R,et al. Premature dissolution of the microsporocyte callose wall causes male sterility in transgenic tobacco[J]. Plant Cell, 1992, 4(7) :759 - 771.

二级参考文献11

  • 1蔡新忠,宋凤鸣,郑重.植物病程相关蛋白[J].植物生理学通讯,1995,31(2):129-136. 被引量:23
  • 2Wei Y,Physiol Mol Plant Pathol,1994年,45卷,469页
  • 3Zhu Q,Bio Technology,1994年,12卷,807页
  • 4李太元,中国科学.B,1994年,24卷,3期,276页
  • 5傅荣昭,植物遗传转化技术手册,1994年
  • 6Zhu Q,Bio Technology,1994年,12卷,807页
  • 7李太元,中国科学.B,1994年,24卷,3期,276页
  • 8傅荣昭,植物遗传转化技术手册,1994年
  • 9贾盘兴,微生物遗传学实验技术,1992年
  • 10蓝海燕,田颖川,张丽华,刘桂珍,王兰岚,陈正华.烟草β-1,3-葡聚糖酶cDNA克隆、大肠杆菌表达及植物表达载体的构建[J].生物工程学报,1998,14(4):412-418. 被引量:5

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