首页> 美国卫生研究院文献>Springer Open Choice >Low Agrobacterium tumefaciens inoculum levels and a long co-culture period lead to reduced plant defense responses and increase transgenic shoot production of sunflower (Helianthus annuus L.)
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Low Agrobacterium tumefaciens inoculum levels and a long co-culture period lead to reduced plant defense responses and increase transgenic shoot production of sunflower (Helianthus annuus L.)

机译:低根癌农杆菌接种水平和较长的共培养时间导致植物防御反应降低并提高向日葵(Helianthus annuus L.)的转基因芽产量。

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摘要

Agrobacterium-mediated plant transformation is typically conducted by inoculating plant tissues with an Agrobacterium suspension containing approximately 108–109 bacteria mL−1, followed by a 2–3-d co-culture period. Use of longer co-culture periods could potentially increase transformation efficiencies by allowing more time for Agrobacterium to interact with plant cells, but bacterial overgrowth is likely to occur, leading to severe tissue browning and reduced transformation and regeneration. Low bacterial inoculum levels were therefore evaluated as a means to reduce the negative outcomes associated with long co-culture. The use of low inoculum bacterial suspensions (approximately 6 × 102 bacteria mL−1) followed by long co-culture (15 d) led to the production of an average of three transformed sunflower shoots per explant while the use of high inoculum (approximately 6 × 108 bacteria mL−1) followed by short co-culture (3 d) led to no transformed shoots. Low inoculum and long co-culture acted synergistically, and both were required for the improvement of sunflower transformation. Gene expression analysis via qRT-PCR showed that genes related to plant defense response were generally expressed at lower levels in the explants treated with low inoculum than those treated with high inoculum during 15 d of co-culture, suggesting that low inoculum reduced the induction of plant defense responses. The use of low inoculum with long co-culture (LI/LC) led to large increases in sunflower transformation efficiency. This method has great potential for improving transformation efficiencies and expanding the types of target tissues amenable for transformation of different plant species.
机译:农杆菌介导的植物转化通常是通过用含有大约10 8 –10 9 细菌mL -1 的农杆菌悬液接种植物组织来进行的,然后2-3天共培养期。通过允许更多时间农杆菌与植物细胞相互作用,使用更长的共培养时间可能潜在地提高转化效率,但是细菌可能过度生长,导致严重的组织褐变和转化和再生减少。因此,评估了低细菌接种量是减少长期共培养相关负面结果的一种手段。使用低接种量的细菌悬浮液(大约6××10 2 细菌mL -1 ),然后长时间共培养(15 d),平均产生每个外植体三个转化的向日葵芽,同时使用高接种量(大约6×10 8 细菌mL -1 ),然后短时间共培养(3 d),导致没有转化芽。低接种量和长时间共培养具有协同作用,两者都是改善向日葵转化所必需的。通过qRT-PCR进行的基因表达分析表明,在共培养15天后,低接种量处理的外植体中的植物防御反应相关基因的表达水平通常比高接种量处理的外植体中的水平低,这表明低接种量可减少对植物防御反应的诱导。植物防御反应。长期共培养(LI / LC)的低接种量的使用大大提高了向日葵转化效率。该方法具有提高转化效率和扩大适于不同植物物种转化的靶组织类型的巨大潜力。

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