Sherrard J H, Kennedy J A, Dalling M J
Plant Sciences Section, School of Agriculture and Forestry, University of Melbourne, Parkville Victoria 3052 Australia.
Plant Physiol. 1979 Sep;64(3):439-44. doi: 10.1104/pp.64.3.439.
When a crude extract from 8-day-old wheat (Triticum aestivum L. cv. Olympic) leaves was fractionated by a combination of ammonium sulfate precipitation and Sephadex G-100 chromatography the presence of three factors which have a marked effect on the stability of highly purified nitrate reductase was revealed. Two of these factors (I and III) have a positive effect and the other factor (II) has a negative effect on stability. Factors I and III can each overcome the instability-promoting effect of II; however, this was apparently not due to a direct effect on factor II.Both factors I and III have been subjected to further purification. Factor I can be separated into at least four fractions, each with stability-promoting activity. Factor III appears to be a single factor.The in vitro activity and stability of nitrate reductase in crude extracts were found to vary diurnally. Stability and activity were highest 4 hours after the start of the light period and both were minimal 1 to 3 hours after the end of the light period. When crude extract was fractionated as described above and an assessment made of the relative amounts of I, II, and III, there appeared to be a distinct diurnal variation in their levels. Factors I and III were highest when in vitro nitrate reductase activity and stability were highest. Factor II was apparently out of phase in that maximum activity coincided with the time of minimum in vitro nitrate reductase activity and stability.
当用硫酸铵沉淀和葡聚糖G - 100柱层析相结合的方法对8日龄小麦(普通小麦品种Olympic)叶片的粗提物进行分级分离时,发现有三种对高纯度硝酸还原酶稳定性有显著影响的因子。其中两种因子(I和III)对稳定性有正向作用,另一种因子(II)对稳定性有负向作用。因子I和III各自都能克服因子II促进不稳定性的作用;然而,这显然不是由于对因子II有直接作用。因子I和III都已进一步纯化。因子I可分离成至少四个组分,每个组分都有促进稳定性的活性。因子III似乎是单一因子。发现粗提物中硝酸还原酶的体外活性和稳定性存在昼夜变化。光照开始后4小时稳定性和活性最高,光照结束后1至3小时两者都最低。当按上述方法对粗提物进行分级分离并评估I、II和III的相对含量时,它们的水平似乎存在明显的昼夜变化。当体外硝酸还原酶活性和稳定性最高时,因子I和III含量最高。因子II显然不同步,其最大活性与体外硝酸还原酶活性和稳定性最低的时间一致。