Department of Agricultural Chemistry, Washington State University, Pullman, Washington 99164.
Plant Physiol. 1980 May;65(5):984-9. doi: 10.1104/pp.65.5.984.
The nitrite-reducing activity of the normal susceptible biotype of lambsquarters (Chenopodium album L.) was strongly inhibited by atrazine in the assay medium, both in the case of the in vivo assays of leaf discs in light, and in vitro photoreduction assays of crude extracts. In vitro assays of crude extracts with methylviologen or ferredoxin supplying the reducing potential were not inhibited by atrazine. In the resistant biotype, inhibition of nitrite reduction did not occur with any of the above assays. Thus, it appears that atrazine does not inhibit nitrite reductase itself, but rather the availability of photosynthetically supplied electrons for the reduction. Atrazine had no effect when added to the media for either in vivo or in vitro assays of nitrate reduction by either the susceptible or resistant biotype.Young lambsquarters plants were treated with atrazine by spraying the leaves at a rate which was lethal for susceptible plants after 5 or 6 days, but had little effect on the resistant biotype. Nitrite did not accumulate in either biotype, but remained present at the level of about 0.1 microgram nitrite N per gram fresh weight. The nitrate content of susceptible-type leaves did increase to two or three times the initial level, during the first four days after spraying. Usually the only visible effect on the plants during this time was a decreased growth rate. Twenty-four hours after spraying the following activities had fallen to 25% or less of the activities of solvent-sprayed control plants: in vivo nitrite reductase, in vivo nitrate reductase, in vitro NADH-nitrate reductase, in vitro reduced flavin mononucleotidenitrate reductase, and in vitro NADH-diaphorase. In these atrazine-treated plants, in vitro nitrite reductase activity with reducing potential supplied by methylviologen was not affected, nor were any of the above activities in leaves of atrazine-treated resistant plants. The abrupt fall in nitrate reductase represents an effect of atrazine not directly related to inhibition of photosynthesis.
正常敏感型猪殃殃(Chenopodium album L.)的亚硝酸盐还原活性在测定介质中被莠去津强烈抑制,无论是在光照下叶片圆盘的体内测定,还是在粗提取物的体外光还原测定中都是如此。用甲基紫精或铁氧还蛋白提供还原潜能的粗提取物的体外测定均不受莠去津抑制。在抗性生物型中,上述任何一种测定都不会抑制亚硝酸盐还原。因此,莠去津似乎不会抑制亚硝酸盐还原酶本身,而是抑制光合作用提供的电子用于还原。在添加到易感性或抗性生物型硝酸盐还原的体内或体外测定的介质中时,莠去津都没有效果。用喷雾法将叶片喷洒到对敏感型植物在 5 或 6 天后致死的莠去津剂量,对抗性生物型几乎没有影响。两种生物型都没有亚硝酸盐积累,但仍保持在约 0.1 微克亚硝酸根氮/克鲜重的水平。在喷洒后的前 4 天,敏感型叶片中的硝酸盐含量增加到初始水平的两到三倍。通常,在此期间对植物的唯一可见影响是生长速度降低。喷洒后 24 小时,以下活性下降到溶剂喷雾对照植物的 25%或以下:体内亚硝酸盐还原酶、体内硝酸盐还原酶、体外 NADH-硝酸盐还原酶、体外还原黄素单核苷酸硝酸盐还原酶和体外 NADH-黄递酶。在这些莠去津处理的植物中,用甲基紫精提供还原潜能的体外亚硝酸盐还原酶活性不受影响,莠去津处理的抗性植物叶片中也没有上述任何一种活性。硝酸盐还原酶的突然下降代表了莠去津的一种效应,与光合作用的抑制没有直接关系。