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首页> 外文期刊>Journal of phycology >Rapid ammonium- and nitrate-induced perturbations to chl a fluorescence in nitrogen-stressed Dunaliella tertiolecta (Chlorophyta)
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Rapid ammonium- and nitrate-induced perturbations to chl a fluorescence in nitrogen-stressed Dunaliella tertiolecta (Chlorophyta)

机译:快速铵和硝酸盐诱导的扰动,使氮胁迫下的杜氏杜氏藻(Chlorophyta)产生荧光

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摘要

When NH4 (+) or NO3 (-) was supplied to NO3 (-) -stressed cells of the microalga Dunaliella tertiolecta Butcher, immediate transient changes in chl a fluorescence were observed over several minutes that were not seen in N-replete cells. These changes were predominantly due to nonphotochemical fluorescence quenching. Fluorescence changes were accompanied by changes in photosynthetic oxygen evolution, indicating interactions between photosynthesis and N assimilation. The magnitude of the fluorescence change showed a Michaelis-Menten relationship with half-saturation concentration of 0.5 muM for NO3 (-) and 10 muM for NH4 (+) . Changes in fluorescence responses were characterized in D. tertiolecta both over 5 days of N starvation and in cells cultured at a range of NO3 (-) -limited growth rates. Variation in responses was more marked in starved than in limited cells. During N starvation, the timing and onset of the fluorescence responses were different for NO3 (-) versus NH4 (+) and were correlated with changes in maximum N uptake rate during N starvation. In severely N-starved cells, the major fluorescence response to NO3 (-) disappeared, whereas the response to NH4 (+) persisted. N-starved cells previously grown with NH4 (+) alone showed fluorescence responses with NH4 (+) but not NO3 (-) additions. The distinct responses to NO3 (-) and NH4 (+) may be due to the differences between regulation of the uptake mechanisms for the two N sources during N starvation. This method offers potential for assessing the importance of NO3 (-) or NH4 (+) as an N source to phytoplankton populations and as a diagnostic tool for N limitation. [References: 48]
机译:将NH4(+)或NO3(-)提供给微藻杜氏藻(Dunaliella tertiolecta Butcher)的NO3(-)胁迫细胞时,在几分钟内观察到chl荧光立即发生瞬时变化,这在N充足的细胞中看不到。这些变化主要是由于非光化学荧光猝灭。荧光变化伴随着光合作用的氧气释放的变化,表明光合作用和氮同化之间的相互作用。荧光变化的幅度显示出Michaelis-Menten关系,其中NO3(-)的半饱和浓度为0.5μM,NH4(+)的半饱和浓度为10μM。在饥饿的5天中,在D. tertiolecta中以及在一定范围的NO3(-)限制的生长速率下培养的细胞中,都表征了荧光响应的变化。饥饿中的反应变化比有限细胞中的变化更为明显。在N饥饿期间,NO3(-)和NH4(+)的荧光响应的时间和开始时间不同,并且与N饥饿期间最大N吸收速率的变化相关。在严重缺氮的细胞中,对NO3(-)的主要荧光反应消失了,而对NH4(+)的反应持续了下来。以前仅使用NH4(+)生长的N饥饿细胞在添加NH4(+)时显示荧光响应,但未添加NO3(-)。对NO3(-)和NH4(+)的不同响应可能是由于N饥饿期间两个N源吸收机制的调节之间的差异。这种方法为评估NO3(-)或NH4(+)作为浮游植物种群的N源和作为N限制诊断工具的重要性提供了潜力。 [参考:48]

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