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衰老的燕麦叶片叶绿体保持光合作用活性。

The retention of photosynthetic activity by senescing chloroplasts of oat leaves.

机构信息

The Thimann Laboratories, University of California, 95064, Santa Cruz, CA, USA.

出版信息

Planta. 1977 Jan;135(2):101-7. doi: 10.1007/BF00387157.

Abstract

The retention of photosystems I and II and or RuDP carboxylase activity in chloroplasts isolated from the first leaves of Victory oat (Avena sativa L.) seedlings was followed as the chloroplasts senesced in darkness. Both photosystems (PS) I and II retained their full activity after 3 days at 1°C, while even after 7 days at 1°C around 80% of the activity was still present. After 3 days at 25°C, PS I lost only 20% and PS II 50% of the initial activity. Acid pH increased the rate of decay of both systems, PS II falling almost to zero after 3 days at pH 3.5 (at 25°C). The preparations were almost bacteria-free, and addition of antibiotics not only did not improve their stability, but accelerated the rates of loss of photosynthetic activity. This is held to indicate that the enzymes are undergoing some turnover even in isolated chloroplasts. If the leaves were allowed to senesce in the dark first and the chloroplasts then isolated, their photosynthetic activities had greatly decreased, showing that senescence is more rapid in situ than in isolation. Under these conditions PS I decayed more rapidly than PS II. Ribulosediphosphate carboxylase, as measured by CO2 fixation, declined more rapidly than the photosystems, though the addition of kinetin and indole-3-acetic acid somewhat decreased the rate of loss, at least for the first 24 h. When the intact (detached) leaves were held in the dark, the rate of oxygen evolution declined rapidly, but in monochromatic blue light (450 nm) at 25°C about 30% of the initial rate was retained after 72 h.

摘要

在黑暗中,随着叶绿体的衰老,从胜利燕麦(Avena sativa L.)幼苗的第一片叶子中分离出的叶绿体中 PS I 和 II 的保留以及 RuDP 羧化酶活性被跟踪。在 1°C 下放置 3 天后,两个光系统(PS)I 和 II 都保留了其全部活性,而即使在 1°C 下放置 7 天后,仍有大约 80%的活性存在。在 25°C 下放置 3 天后,PS I 仅损失初始活性的 20%,PS II 损失 50%。酸性 pH 增加了两个系统的衰变速率,PS II 在 pH 3.5(在 25°C 下)下放置 3 天后几乎降至零。这些制剂几乎没有细菌,添加抗生素不仅没有提高它们的稳定性,反而加速了光合活性丧失的速度。这表明即使在分离的叶绿体中,酶也在进行一些周转。如果先让叶片在黑暗中衰老,然后再分离叶绿体,它们的光合活性会大大降低,这表明衰老在体内比在分离时更快。在这些条件下,PS I 的衰减速度快于 PS II。用 CO2 固定测量的核酮糖二磷酸羧化酶的下降速度比光系统更快,尽管添加激动素和吲哚-3-乙酸在至少前 24 小时内会降低失活速率。当完整(分离)的叶片在黑暗中时,氧气释放的速度迅速下降,但在 25°C 的单色蓝光(450nm)下,经过 72 小时后,仍保留了初始速率的约 30%。

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