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首页> 外文期刊>Journal of Plant Physiology >Osmotic induced stimulation of the reduction of the viability dye 2,3,5-triphenyltetrazolium chloride by maize roots and callus cultures
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Osmotic induced stimulation of the reduction of the viability dye 2,3,5-triphenyltetrazolium chloride by maize roots and callus cultures

机译:渗透诱导的玉米根和愈伤组织培养物减少活性染料2,3,5-三苯基四唑鎓氯化物的刺激

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摘要

Live cells can reduce colorless 2,3,5-triphenyltetrazolium chloride (TTC) to a red insoluble compound, formazan. Maize (Zea mays) callus, when osmotically stressed by 0.53 mol/L mannitol, produced 7-times or more formazan than untreated control callus, This result was seen with all osmotica tested and could not be attributed to differences in TTC uptake rate or accumulation, increased respiration rate as measured by O-2 uptake, or to de,novo protein synthesis, Increased formazan production could be detected after 2.5 h of exposure to osmotic stress and leveled off after 48 h of exposure. The increased formazan production was only detected when callus was moved from high osmotic medium to low osmotic, TTC-containing medium. Abscisic acid increased TTC reduction only when added in combination with 0.53 mol/L mannitol. Incubation of maize seedling roots with 0.53mol/L mannitol also increased formazan produc ion as seen visually. Further studies are needed to determine the cause of the increased formazan production. These results show that TTC viability measurements must be carefully evaluated with appropriate controls to confirm their validity.
机译:活细胞可以将无色的2,3,5-三苯基四唑氯化物(TTC)还原为红色的不溶化合物甲for。玉米(Zea mays)愈伤组织在受到0.53 mol / L甘露醇的渗透胁迫时,产生的甲for是未经处理的对照愈伤组织的7倍或更多。此结果在所有渗透试验中均可见,不能归因于TTC摄取率或积累的差异,如通过O-2摄取测量的呼吸速率增加,或为了合成新蛋白,在暴露于渗透压2.5 h后可检测到甲for产量增加,并在暴露48 h后趋于稳定。仅当愈伤组织从高渗透性培养基移至低渗透性,含TTC的培养基中时,甲for的产量才会增加。脱落酸仅当与0.53 mol / L甘露糖醇组合使用时才提高TTC的降低。肉眼观察到,用0.53mol / L甘露醇孵育玉米幼苗根部也增加了甲maz的生产。需要进一步研究以确定甲for产量增加的原因。这些结果表明,必须通过适当的控制措施仔细评估TTC的生存力,以确认其有效性。

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