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作 者:桑敏[1,2] 秦晓春[2] 王文达[2] 陈晓波[3] 谢杰[4] 李良璧[2] 匡廷云[2]
机构地区:[1]暨南大学水生生物研究中心,广州510632 [2]中国科学院植物研究所光合作用与环境分子生理学重点实验室,北京100093 [3]河北科技大学生物科学与工程学院,石家庄050018 [4]中国科学院化学研究所光化学重点实验室,北京100080
出 处:《生物物理学报》2012年第10期848-854,共7页Acta Biophysica Sinica
基 金:supported by grants from the "973" Programs(2009CB118501 and 2011CBA00901);the National Natural Science Foundation of China(30900095);Foundation for Distinguished Young Talents in Higher Education of Guangdong,China(LYM11025);the Fundamental Research Funds for the Central Universities(11612325 and 11612352)~~
摘 要:采用自旋捕捉电子顺磁共振技术研究了强光诱导下菠菜Cyt b6f中单线态氧(1O2*)产生和清除的分子机制,结果表明:在强光照射和有氧条件下,缺失Rieske Fe-S蛋白的Cytb6f和分离的Rieske Fe-S蛋白溶液中都检测到1O2*的产生,这证明Chla和Rieske Fe-S蛋白都是菠菜Cytb6f中光诱导1O2*产生的位点,而Chla是1O2*产生的主要部位。采用波长为675 nm的红光选择性激发Cytb6f中的Chla时,也检测到1O2*的产生,进一步支持了上述结论。此外,外加天然抗氧化物质,如抗坏血酸、谷胱甘肽、L-组氨酸和β-胡萝卜素,可清除系统中产生的1O2*。这很可能是菠菜Cytb6f中一种保护底物抵抗单线态氧光氧化的保护机制。Electron spin resonance spectroscopy was used to study the mechanism of the singlet oxygen (1O2*) production and scavenging in cytochrome b6f complex (Cyt bet) of spinach. The results showed that under white-light illumination and aerobic conditions, 1O2* was detected in isolated Rieske-depleted Cyt b6f and isolated Rieske Fe-S protein, indicating that both Chl a cofactor and Rieske Fe-S protein were responsible for 1O2* formation, with Chl a being the major source. This conclusion was further corroborated by 1O2* formation under selective excitation of Chl a by using monocolor red light at 675 nm. Furthermore, 1O2* was scavenged by adding antioxidative substance such as L-histidine, ascorbate, β-carotene or glutathione. This offered protection against singlet oxygen oxidation of Cyt bf complex.
关 键 词:叶绿素A 细胞色素b6f蛋白复合体 单线态氧 光保护 电子顺磁共振
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