Pflanzenphysiologisches Institut der Universität Bern, Altenbergrain 21, CH-3013 Bern, Switzerland.
Plant Physiol. 1978 Mar;61(3):342-7. doi: 10.1104/pp.61.3.342.
When 0.5 mm cysteine is added to cultures of Lemna minor L. growing with sulfate as the sole sulfur source, there is a rapid 80% loss of extractable adenosine 5'-phosphosulfate sulfotransferase. This loss is accompanied by an inhibition of sulfate uptake; however, lack of sulfate is not responsible for the decreasing adenosine 5'-phosphosulfate sulfotransferase activity.Cultivation with cysteine causes an increase in the cyst(e)ine pool of L. minor. This fact taken together with the observed inactivation of adenosine 5'-phosphosulfate sulfotransferase in crude extracts by cysteine suggests that the cysteine pool is involved in the in vivo regulation of the enzyme.The activity of adenosine 5'-phosphosulfate sulfotransferase is restored within 24 hours after transfer to a culture medium without cysteine. This restoration is partially blocked by 6-methyl purine and actinomycin D and completely by cycloheximide.Cycloheximide added to cultures of L. minor L. causes a loss of extractable APSTase comparable to the one obtained with cysteine. This loss may be in part due to cysteine, since cycloheximide causes a pronounced increase in the cysteine pool of L. minor.
当 0.5 毫米半胱氨酸被添加到以硫酸盐作为唯一硫源生长的浮萍( Lemna minor L. )培养物中时,可迅速导致 80%的可提取腺苷 5'-磷酸硫酸转移酶损失。这种损失伴随着硫酸盐摄取的抑制;然而,缺乏硫酸盐并不是导致腺苷 5'-磷酸硫酸转移酶活性降低的原因。培养物中半胱氨酸的存在会导致浮萍的半胱氨酸池增加。考虑到观察到的粗提取物中半胱氨酸对腺苷 5'-磷酸硫酸转移酶的失活,这一事实表明,半胱氨酸池参与了该酶的体内调节。在转移到不含半胱氨酸的培养基中 24 小时内,腺苷 5'-磷酸硫酸转移酶的活性得到恢复。该恢复过程部分被 6-甲基嘌呤和放线菌素 D 阻断,完全被环己酰亚胺阻断。环己酰亚胺添加到浮萍( Lemna minor L. )的培养物中会导致可提取的 APSTase 丧失,这与用半胱氨酸获得的结果相当。这种损失可能部分归因于半胱氨酸,因为环己酰亚胺会导致浮萍的半胱氨酸池明显增加。