Department of Biological Sciences, University of Lancaster, LA1 4YQ, Lancaster, UK.
Planta. 1974 Jan;121(3):273-82. doi: 10.1007/BF00389327.
A quantitative estimation of sodium dodecyl sulphate-extractable plastid envelope polypeptides during greening of Avena sativa L. laminae is described, combined with protein distribution and plastid number studies over the same period.A primary light-dependent and cytoplasm-dependent increase in both total plastid protein and envelope associated protein during the first 30 minutes of greening was observed, followed by a period during which release of envelope-associated protein either into the plastid or into the cytoplasm, or both, takes place. After 8 hours greening an increase in plastid envelope protein reflects a requirement for an increased plastid surface area during chloroplast maturation.A comparison of the behaviour of envelope membranes during illuminated in vitro incubation of isolated etio-plasts with plastids isolated from tissue given similar illumination pre-treatments, indicates that the early increase in envelope-associated protein is real and requires the participation of the cytoplasm.
描述了在燕麦叶片变绿过程中十二烷基硫酸钠可提取质体被膜多肽的定量估计,同时还结合了同期的蛋白质分布和质体数量研究。在变绿的最初 30 分钟内,观察到总质体蛋白和与被膜结合的蛋白都出现了一次依赖于光和细胞质的主要增加,之后是一个时期,在此期间,被膜结合蛋白被释放到质体或细胞质中,或者两者兼而有之。变绿 8 小时后,质体被膜蛋白的增加反映了在叶绿体成熟过程中需要增加质体表面积。将离体黄化质体在光照下体外培养与组织中分离的质体进行比较,发现早期被膜相关蛋白的增加是真实的,需要细胞质的参与。