Trewavas A
Biological Sciences, University of East Anglia, Norwich, England.
Plant Physiol. 1970 Jun;45(6):742-51. doi: 10.1104/pp.45.6.742.
A method is described for measuring the rate constants of both synthesis and degradation of nucleic acids in sterile growing cultures of Lemna minor which avoids the difficulties of environmental changes in isotope uptake and precursor pool size. In fast growing cultures the half-life of ribosomal RNA has been estimated to be between 5 and 8 days.This half-life has been shown to consist of two components, cytoplasmic ribosomal RNA with a half-life of about 4 days and chloroplast ribosomal RNA with a half-life of about 15 days. The possible interference of recycling has been checked, and the evidence indicates its likely insignificance. "Heavy" labeling of Lemna with D(2)O and (15)NO(-) (3) has provided evidence for the conservation of ribosomal RNA in fast growing cultures and has also provided an alternative assessment of recycling. When Lemna is placed on water, the rate of degradation of ribosomal RNA is increased and that of synthesis is decreased. Under partial "step down" conditions it has been found that omission of either nitrate or phosphate, or calcium or magnesium leads to an increase in the rate of degradation of ribosomal RNA. In Lemna grown on water, benzyladenine increases both the synthetic and degradative rates of nucleic acid metabolism. Abscisic acid, on the other hand, markedly reduces the rate of synthesis of ribosomal RNA but leaves the degradative rate unaltered.
本文描述了一种测量小浮萍无菌生长培养物中核酸合成和降解速率常数的方法,该方法避免了同位素摄取和前体库大小环境变化带来的困难。在快速生长的培养物中,核糖体RNA的半衰期估计在5到8天之间。已证明这个半衰期由两个部分组成,细胞质核糖体RNA的半衰期约为4天,叶绿体核糖体RNA的半衰期约为15天。已检查了再循环可能产生的干扰,证据表明其可能并不重要。用D₂O和¹⁵NO₃⁻对小浮萍进行“重”标记,为快速生长培养物中核糖体RNA的保守性提供了证据,也为再循环提供了另一种评估方法。当小浮萍置于水中时,核糖体RNA的降解速率增加,合成速率降低。在部分“逐步降低”条件下,已发现省略硝酸盐或磷酸盐、钙或镁会导致核糖体RNA降解速率增加。在水中生长的小浮萍中,苄基腺嘌呤会增加核酸代谢的合成和降解速率。另一方面,脱落酸会显著降低核糖体RNA的合成速率,但降解速率不变。