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叶绿素发光的一个一微秒成分表明光合作用系统II的初级受体不同于Q。

A one microsecond component of chlorophyll luminescence suggesting a primary acceptor of system II of photosynthesis different from Q.

作者信息

Van Best J A, Duysens L N

出版信息

Biochim Biophys Acta. 1977 Feb 7;459(2):187-206. doi: 10.1016/0005-2728(77)90021-4.

Abstract

The kinetics of the luminescence of chlorophyll a in Chlorella vulgaris were studied in the time range from 0.2 mus to 20 mus after a short saturating flash (t 1/2 = 25 ns) under various pretreatment including anaerobiosis, flashes, continuous illumination and various additions. A 1 mus luminescence component probably originating from System II was found of which the relative amplitude was maximum under anaerobic conditions for reaction centers in the state SPQ- before the flash, about one third for centers in the state S+PQ- or SPQ before the flash, and about one tenth for centers in the state S+PQ before the flash. S is the secondary donor complex with zero change; S+ is the secondary donor complex with 1 to 3 positive charges; P, the primary donor, is the photoactive chlorophyll a, P-680, of reaction center 2; Q- is the reduced acceptor of System II, Q. Under aerobic conditions, where an endogenous quencher presumably was active, the luminescence was reduced by a factor two. The 1 mus decay of the luminescence is probably caused by the disappearance of P+ formed in the laser flash according to the reaction ZP+ leads to Z+ in which Z is the molecule which donates an electron to P+ and which is part of S. After addition of hydroxylamine, the 1 mus luminescence component changed with the incubation time exponentially (tau = 27 s) into a 30 mus component; during the same time, the variable fluorescence yield, measured 9 mus after the laser flash, decreased by a factor 2 with the same time constant. Hereafter in a second much slower phase the fluorescence yield decreased as an exponential function of the incubation time to about the dark value; meanwhile the 30 mus luminescence increased about 50% with the same time constant (tau = 7 min). Heat treatment abolished both luminescence components. The 1 mus luminescence component saturated at about the same energy as the System II fluorescence yield 60 mus after the laser flash and as the slower luminescence components. From the observation that the amplutide is maximum if the laser flash is given when the fluorescence yield is high after prolonged anaerobic conditions (state SQ-), we conclude that the 1 mus luminescence is probably caused by the reaction PWQ- + hv leads to PWQ- leads to P+W-Q- leads to PWQ- leads to PWQ- + hv in which W is an acceptor different from Q. The presence of S+ reduced the luminescence amplitude to about one third. Two models are discussed, one with W as an intermediate between P and Q and another, which gives the best interpretation, with W on a side path.

摘要

在各种预处理条件下,包括厌氧、闪光、连续光照以及添加各种物质后,研究了小球藻中叶绿素a在短饱和闪光(t 1/2 = 25纳秒)后0.2微秒至20微秒时间范围内的发光动力学。发现了一个可能源自光系统II的1微秒发光成分,其相对幅度在闪光前处于SPQ - 状态的反应中心厌氧条件下最大,在闪光前处于S + PQ - 或SPQ状态的中心约为三分之一,在闪光前处于S + PQ状态的中心约为十分之一。S是电荷为零的二级供体复合物;S + 是带有1至3个正电荷的二级供体复合物;P,初级供体,是反应中心2的光活性叶绿素a,P - 680;Q - 是光系统II的还原受体,Q。在有氧条件下,内源性猝灭剂可能起作用,发光降低了一半。发光的1微秒衰减可能是由于激光闪光中形成的P + 根据反应ZP + → Z + 消失导致的,其中Z是向P + 提供电子的分子,是S的一部分。添加羟胺后,1微秒发光成分随孵育时间呈指数变化(τ = 27秒)转变为30微秒成分;同时,在激光闪光后9微秒测量的可变荧光产率以相同的时间常数降低了一半。此后,在第二个慢得多的阶段,荧光产率作为孵育时间的指数函数降低至约暗值;与此同时,30微秒发光以相同的时间常数(τ = 7分钟)增加了约50%。热处理消除了这两个发光成分。1微秒发光成分在激光闪光后60微秒时与光系统II荧光产率以及较慢的发光成分在大致相同的能量下达到饱和。从在长时间厌氧条件(SQ - 状态)后荧光产率高时给予激光闪光时幅度最大这一观察结果,我们得出结论,1微秒发光可能是由反应PWQ - + hv → P * WQ - → P + W - Q - → P * WQ - → PWQ - + hv引起的,其中W是不同于Q的受体。S + 的存在使发光幅度降低至约三分之一。讨论了两种模型,一种是W在P和Q之间作为中间体,另一种能给出最佳解释,即W在一条侧支途径上。

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