Weed Science Lab, USDA-S, 38776, Stoneville, MS.
Photosynth Res. 1985 Jan;6(2):113-20. doi: 10.1007/BF00032786.
Previous studies in our laboratory have shown that tentoxin prevents the incorporation of polyphenol oxidase (PPO), a nuclearly-coded protein, into the chloroplasts of sensitive species. In this study, we show, by comparison of electrophoretically separated isozymes, that ferredoxin-NADP(+) reductase (FNR) is nuclearly coded in Nicotiana. Electrophoresis of FNR isozymes from tentoxin treated seedlings of a sensitive and a resistant species demonstrated that, unlike PPO, ferredoxin-NADP(+) reductase was unaffected by tentoxin treatment. These data indicate that tentoxin selectively inhibits transport of cytoplasmically synthesized proteins into the chloroplast, and does not produce a generalized disruption of cellular integration.
先前在我们实验室进行的研究表明, tentoxin 可阻止核编码蛋白多酚氧化酶(PPO)掺入敏感物种的叶绿体。在这项研究中,我们通过比较电泳分离的同工酶表明,Nicotiana 中的铁氧还蛋白-NADP(+)还原酶(FNR)是核编码的。与 PPO 不同,用 tentoxin 处理敏感和抗性物种的幼苗后电泳分离 FNR 同工酶表明,铁氧还蛋白-NADP(+)还原酶不受 tentoxin 处理的影响。这些数据表明,tentoxin 选择性地抑制细胞质合成的蛋白质向叶绿体的转运,而不会导致细胞整合的普遍破坏。