Stemler A
Biochim Biophys Acta. 1980 Nov 5;593(1):103-12. doi: 10.1016/0005-2728(80)90011-0.
In broken chloroplasts the presence of 100 mM sodium formate at pH 8.2 will specifically lengthen the Photosystem II relaxation times of the reactions S'2 leads to S3 and S'3 leads to S0. Rates of reactions S'0 leads to S1 and S'1 leads to S2 remain unaffected. Evidence is presented which indicates the discrimination among S-states by formate cannot be attributed to a block imposed on the reducing side of Photosystem II. The results are interpreted in context of the known interaction of formate and CO2 which is bound to the Photosystem II reaction center complex. It is proposed that those S-state transitions which show extended relaxation times in the presence of formate must result in the momentary release and rebinding of CO2. Furthermore since formate is acting on the oxygen-evolving side of Photosystem II, it would seem that CO2 is released in reactions that occur there. A chemical model of oxygen evolution is presented. It is based on the hypothesis that hydrated CO2 is the immediate source of photosynthetically evolved oxygen and explains why, under certain conditions formate slows only the S-state transitions S'2 leads to S3 and S'3 leads to S0.
在破碎的叶绿体中,在pH 8.2条件下存在100 mM甲酸钠会特异性延长反应S'2→S3和S'3→S0的光系统II弛豫时间。反应S'0→S1和S'1→S2的速率不受影响。有证据表明,甲酸盐对S态的区分不能归因于对光系统II还原侧施加的阻断。结合甲酸盐与CO2已知的相互作用(CO2与光系统II反应中心复合物结合)对结果进行了解释。有人提出,那些在甲酸盐存在下显示弛豫时间延长的S态转变必定导致CO2的瞬间释放和重新结合。此外,由于甲酸盐作用于光系统II的放氧侧,似乎CO2是在那里发生的反应中释放的。提出了一个放氧的化学模型。它基于水合CO2是光合放氧的直接来源这一假设,并解释了为什么在某些条件下甲酸盐仅减缓S态转变S'2→S3和S'3→S0。