Charles F. Kettering Research Laboratory, Yellow Springs, Ohio 45387.
Plant Physiol. 1970 Nov;46(5):699-704. doi: 10.1104/pp.46.5.699.
Chloroplasts were isolated from wild type (DG) and heterozygous mutant (LG) soybean (Glycine max) leaves, and various biochemical functions were compared. Noncyclic electron transport, and its coupled phosphorylation, cyclic phosphorylation and H(+) ion transport in both systems, were 3 to 5 times faster in rate (on a chlorophyll basis) in the mutant plastids. On a chloroplast lamellar protein basis, the mutant plastid rates were 1.5 to 2.5 times the wild type rates.Plastoquinone (PQ) reduction and oxidation (rates and extent) were measured by following absorbance changes at 260 nanometers with the repetitive flash technique. Mutant plastids have about a 2-fold greater apparent first order rate constant for PQ oxidation and a 3- to 5-fold larger pool of rapidly reducible PQ. Plastoquinone oxidation has been identified by other workers as the rate-limiting step in electron transport. Assuming the PQ oxidation is a first order process (d(PQH(2))/dt = k(D)[PQH(2)]t), the observed increase in k(d) for the LG (k(d) (LG) approximately 2k(d) (DG)) and the greater steady state amount of rapidly turning over PQ, PQH(2)>PQH(2), could account for the 3- to 5-fold greater rates of electron transport and phosphorylation found in the mutant chloroplasts.Light saturation for noncyclic photophosphorylation and photosystem 2 plus 1 electron transport occurred at similar intensities for both LG and DG plastids. Relative quantum requirements extrapolated to zero intensity were similar in the LG and DG, although at finite light intensities the LG had a better relative quantum efficiency.Ammonium chloride concentrations needed to inhibit cyclic photophosphorylation 50% were similar in both LG and DG plastids. Nigericin, poly-l-lysine, and chlorotri-n-butyltin, were needed in concentrations 5 to 10 times greater in the LG to yield 50% inhibition at comparable chlorophyll concentrations.
从野生型(DG)和杂合突变体(LG)大豆(Glycine max)叶片中分离出叶绿体,并比较了它们的各种生化功能。在突变体叶绿体中,非循环电子传递及其偶联的磷酸化、循环磷酸化和 H+离子转运的速率(按叶绿素基础)比野生型快 3 到 5 倍。按叶绿体层状蛋白基础计算,突变体叶绿体的速率是野生型的 1.5 到 2.5 倍。通过重复闪光技术跟踪 260 纳米处的吸光度变化,测量质体醌(PQ)的还原和氧化(速率和程度)。突变体叶绿体的表观一级 PQ 氧化速率常数约为 2 倍,可迅速还原的 PQ 池约为 3 到 5 倍。其他研究人员已将质体醌氧化鉴定为电子传递的限速步骤。假设 PQ 氧化是一个一级过程(d(PQH2)/dt = k(D)[PQH2]t),LG 中观察到的 k(d)增加(k(d)(LG)约为 2k(d)(DG))和可迅速周转的 PQ 量增加,[PQH2](LG)>[PQH2](DG),可以解释在突变体叶绿体中发现的 3 到 5 倍更高的电子传递和磷酸化速率。非循环光磷酸化和 PS2+1 电子传递的光饱和发生在 LG 和 DG 叶绿体的相似强度下。LG 和 DG 的相对量子需求在有限光强度下趋于零,尽管在有限光强度下,LG 具有更好的相对量子效率。抑制循环光磷酸化 50%所需的氯化铵浓度在 LG 和 DG 叶绿体中相似。在可比叶绿素浓度下,需要用尼日尔菌素、多聚-L-赖氨酸和三丁基氯化锡将 LG 抑制 50%,浓度要高 5 到 10 倍。