胼胝质

pián zhī zhì
  • callose
胼胝质胼胝质
  1. PMC胼胝质壁的形成是在花粉母细胞时期开始的;

    The formation of the callose wall occured at the PMC stage .

  2. 蓼型(Polygonum-type)胚囊大孢子母细胞减数分裂时,其珠孔端细胞壁出现胼胝质荧光,并逐渐扩展到整个细胞壁。

    Polygonum-type & During the process of megasporocyte meiosis , callose occurs first in the wall of megasporocyte from micropylar end , then gradually envelops the whole cell .

  3. NaCl处理后的柱头乳突细胞胼胝质含量的变化与亲和性变化有相同趋势。

    The amount of callose in surface cells of the stigma and the incompatibility after treatment with NaCl solution tended to change in the same direction .

  4. 结果表明,韭型(Alliumodorum-type)胚囊大孢子发生时,自大孢子母细胞的珠孔端细胞壁内出现胼胝质荧光,并逐渐扩展到整个细胞壁,中期Ⅰ至末期Ⅰ细胞壁呈现胼胝质荧光。

    The results are as follows : Allium odorum-type & Callose first occurs in the wall of megasporocyte from the micropylar end , then gradually envelops the whole cell . Megasporocyte is surrounded by the wall with callose during metaphase ⅰ, anaphase ⅰ and telephase ⅰ .

  5. 过敏性坏死反应和胼胝质的形成是2个重要的抗锈机制。

    Hypersensitive reaction and callose formation were two important resistance mechanisms .

  6. 不亲和的花粉管首先是被果胶质堵塞,接着是胼胝质沉积。

    Incompatible pollen is blocked initially by pectins followed by callose deposition .

  7. 受侵寄主细胞分泌的胼胝质,可将吸器体完全包围。

    The collars formed in infected host cells could surround the haustoria .

  8. 胼胝质的染剂是苯胺蓝,间苯二酚蓝和玫红酸。

    Callose stains are aniline blue , resorcin blue and rosolic acid .

  9. 黑麦小孢子母细胞形成和发育过程中细胞胼胝质壁合成的变化

    Change of callose wall synthesis during formation and development of microsporocytes in Secale cereale

  10. 掌叶大黄胚珠的发育及胼胝质的变化

    Ovule development and callose deposition in Rheum palmatum

  11. 被子植物有性和无融合生殖过程中胼胝质壁的动态变化及其生物学意义

    Changes and Biological Significance of Callose Wall in Sexual Reproduction and Apomixis of Angiosperms

  12. 水松花粉中的淀粉粒和胼胝质

    Starch Grain and Callus of Pollen in Glyptostrobus Pensilis ( Staunt . ) Koch

  13. 简要阐述了花粉管胼胝质和酚类含量在硼胁迫时的异常表现。

    Abnormalities of the content and distribution of callose and phenolics are also mentioned .

  14. 质壁分离处理产生的胼胝质与体细胞胚发生呈正相关。

    There was positive correlation between somatic embryogenesis and callose produced after plasmolysis treatment .

  15. 侧壁通常不具胼胝质。

    But the side walls usually lacked callose .

  16. 发育后期,则具有胼胝质壁,直至细胞解体。

    In late development stage , they have callose wall , until the cells disintegrate .

  17. 自交花粉管因胼胝质在壁上添加而停止生长。

    The self-pollinated pollen tubes stopped growing as the callose added on the cell wall .

  18. 营养细胞和生殖细胞周围及其之间具有明显的胼胝质荧光。

    There is obvious fluorescence of the callous around and between vegetative and generative cells .

  19. 大孢子母细胞时期细胞壁内缺少胼胝质。

    The wall of the generative cell contains callose . Callose was absent at megasporocyte stage .

  20. 花粉管中胼胝质沿管壁不规则沉积,有的不形成胼胝质塞,或整个管壁被胼胝质所覆盖。

    Random deposition of callose along pollen tube wall and even the whole wall was observed .

  21. 第一次减数分裂前期的合点壁上最先出现胼胝质并显示连续的荧光。

    It first appeared at the chalazal wall during the first meiotic prophase and exhibited continuous fluorescence .

  22. 禾本科植物的花粉管在柱头的表面被果胶质和胼胝质堵塞。

    In the grasses the pollen tube is blocked at the stigma surface with pectins and callose .

  23. 胼胝质在大小孢子发生期间,有规律地出现与降解。

    Callose in the size of the spores in the period , a pattern of occurrence and degradation .

  24. 导致小孢子败育的原因与四分体胼胝质壁不适时解体和绒毡层细胞发育异常、延迟解体有关。

    The abnormality of tetrad callose wall degradation and tapetum development was associated with the abortion of microspore .

  25. 胚性愈伤组织中可观察到大量胼胝质的沉积,而非胚性愈伤组织中观察不到胼胝质的沉积。

    A number of callose deposition can be observed in embryonic calli , but not in non-embryonic calli .

  26. 因此,亲和组合中胞间连丝上没有胼胝质积累从而使病毒能够进行细胞间运输。

    So there was no callose deposited at PD and viruses could transport between cells in the compatible combination .

  27. 退化的大孢子细胞壁胼胝质荧光明显,功能大孢子细胞壁上缺少胼胝质荧光。

    Thick callose deposits in the walls of degenerative megaspores , while little in the wall of functional megaspore .

  28. 二分体、三分体、四分体时期,胼胝质荧光主要存在于大孢子之间的横壁上,侧壁内胼胝质荧光较弱。

    Callose exists mainly in transverse walls during dyad , triad and tetrad stages , a little in side walls .

  29. 药室内壁、中层层数增加,绒毡层细胞肥大,造孢细胞或花粉母细胞分解解体;⑤由于花粉母细胞胼胝质壁不降解而无法释放出四分体小孢子;

    Cell layers of powder chamber wall and middle-level were increased , tapetum cells were hypertrophied and microsporogenesis or microspore disaggregated ;

  30. 因此,黄瓜感染病原菌后,根、叶柄内形成大量胼胝质,限制了水分运输,降低了叶片含水量和光合速率是黄瓜连作障碍的原因之一。

    Therefore , the formation of callose in infected plants restrained water transport , and decreased leaf water content and photosynthesis .