首页> 外文期刊>Biochimica et biophysica acta. Bioenergetics >Utilization of blue-green light by chlorosomes from the photosynthetic bacterium Chloroflexus aurantiacus: Ultrafast excitation energy conversion and transfer
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Utilization of blue-green light by chlorosomes from the photosynthetic bacterium Chloroflexus aurantiacus: Ultrafast excitation energy conversion and transfer

机译:从光合细菌的氯瓜瓜瓜氏菌的氯瓜瓜菌的利用利用氯吡咯:超快激励能量转换和转移

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摘要

Chlorosomes of photosynthetic green bacteria are unique molecular assemblies providing efficient light harvesting followed by multi-step transfer of excitation energy to reaction centers. In each chlorosome, 10(4)-10(5) bacteriochlorophyll (BChl) c/d/e molecules are organized by self-assembly into high-ordered aggregates. We studied the early-time dynamics of the excitation energy flow and energy conversion in chlorosomes isolated from Chloroflexus (Cfx.) aurantiacus bacteria by pump-probe spectroscopy with 30-fs temporal resolution at room temperature. Both the S-2 state of carotenoids (Cars) and the Soret states of BChl c were excited at similar to 490 nm, and absorption changes were probed at 400-900 nm. A global analysis of spectroscopy data revealed that the excitation energy transfer (EET) from Cars to BChl c aggregates occurred within similar to 100 fs, and the Soret -> Q energy conversion in BChl c occurred faster within similar to 40 fs. This conclusion was confirmed by a detailed comparison of the early exciton dynamics in chlorosomes with different content of Cars. These processes are accompanied by excitonic and vibrational relaxation within 100-270 fs. The well-known EET from BChl c to the baseplate BChl a proceeded on a ps time-scale. We showed that the S-1 state of Cars does not participate in EET. We discussed the possible presence (or absence) of an intermediate state that might mediates the Soret -> Q(y) internal conversion in chlorosomal BChl c. We discussed a possible relationship between the observed exciton dynamics and the structural heterogeneity of chlorosomes.
机译:光合绿色细菌的氯运动是独特的分子组件,提供有效的光收获,然后进行激发能量的多步转移到反应中心。在每种氯体组上,通过自组装成高值的聚集体组织10(4)-10(5)氯苯氯(BCHL)C / D / E分子。通过泵探针光谱法在室温下泵探针光谱研究了从氯仿(CFX。)Aurantiacus菌中分离的氯蛋白酶中的激发能量流量和能量转化的早期动态。在类似于490nm的同样为490nm的S-2类胡萝卜素(汽车)和Soret状态都是激发的,并且探测400-900nm的吸收变化。对光谱数据的全局分析表明,从汽车到BCH1 C聚集体的激发能量转移(EET)在类似于100 fs的情况下发生,并且BCHL C中的Soret - > Q能量转换类似于类似于40 fs的速度更快。通过不同含量的氯运动瘤中早期激子动态的详细比较证实了这一结论。这些过程伴随着100-270 fs内的激子和振动松弛。从BCHL C到底板BCHL A的众所周知的EET在PS时间尺度上进行。我们表明S-1汽车状态不参加EET。我们讨论了可能在氯 - β(y)内转化中的中间状态的可能存在(或不存在)中的中间状态在氯聚酯BCH1 C中的内转化。我们讨论了观察到的激子动态与氯体的结构异质性之间的可能关系。

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