Fuller R C, Nugent N A
Proc Natl Acad Sci U S A. 1969 Aug;63(4):1311-8. doi: 10.1073/pnas.63.4.1311.
The photoreduction and interaction with the photosynthetic "reaction center" of 2-amino,4-hydroxy-6-substituted pteridine indicates that these low-potential ( approximately -0.7 v), naturally occurring compounds play a primary role in photosynthetic electron transport. These unconjugated pteridines, which occur in association with the photosynthetic apparatus of green plants and photosynthetic bacteria, can be reduced by light in the presence of a bacterial chromatophore fraction from the dihydro form to the tetrahydro form. 6,7-Dimethyl-tetrahydropteridine readily reduces spinach ferredoxin. This compound also specifically interacts with reaction-center chlorophyll and bacteriochlorophyll and produces spectral shifts similar to those produced by light. It is proposed that the electron produced by excited-state chlorophyll is captured and separated by a pteridine at -0.67 v at the photosynthetic reaction center.
2-氨基-4-羟基-6-取代蝶啶的光还原作用及其与光合“反应中心”的相互作用表明,这些低电位(约-0.7伏)的天然存在化合物在光合电子传递中起主要作用。这些未共轭的蝶啶与绿色植物和光合细菌的光合装置相关联,在存在来自细菌载色体部分的情况下,可通过光照从二氢形式还原为四氢形式。6,7-二甲基四氢蝶啶很容易还原菠菜铁氧还蛋白。该化合物还与反应中心叶绿素和细菌叶绿素特异性相互作用,并产生与光照产生的光谱位移相似的光谱位移。有人提出,激发态叶绿素产生的电子在光合反应中心被-0.67伏的蝶啶捕获并分离。