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除草剂异恶草酮并不抑制体外由甲羟戊酸合成香叶基香叶基的过程。

Herbicide clomazone does not inhibit in vitro geranylgeranyl synthesis from mevalonate.

作者信息

Weimer M R, Balke N E, Buhler D D

机构信息

Department of Agronomy, University of Wisconsin, Madison, Wisconsin 53706.

出版信息

Plant Physiol. 1992 Feb;98(2):427-32. doi: 10.1104/pp.98.2.427.

Abstract

Clomazone reduced the chlorophyll and carotenoid contents of spinach (Spinacia oleracea L.), barley (Hordeum vulgare L.), velvetleaf (Abutilon theophrasti Medik.), and soybean (Glycine max L. Merr.) seedlings. The order of species sensitivity was velvetleaf > spinach > barley > soybean. Clomazone (100 micromolar) did not affect the in vitro activities of spinach isopentenyl pyrophosphate isomerase or prenyl transferase. Clomazone also did not affect the synthesis of isopentenyl pyrophosphate from mevalonic acid. Thus, clomazone had no direct in vitro effect on the synthesis of geranylgeranyl pyrophosphate from mevalonic acid. Greening seedlings of both soybean and velvetleaf metabolized clomazone. No qualitative differences in the metabolites were detected between soybean and velvetleaf. Thus, differential metabolism of clomazone to a toxic chemical that inhibits terpenoid synthesis is unlikely. Clomazone has either a mode of action not yet identified or a metabolite that is selective in that it is much more active in sensitive than tolerant species.

摘要

异恶草酮降低了菠菜(Spinacia oleracea L.)、大麦(Hordeum vulgare L.)、苘麻(Abutilon theophrasti Medik.)和大豆(Glycine max L. Merr.)幼苗的叶绿素和类胡萝卜素含量。物种敏感性顺序为苘麻>菠菜>大麦>大豆。异恶草酮(100微摩尔)不影响菠菜异戊烯基焦磷酸异构酶或异戊烯基转移酶的体外活性。异恶草酮也不影响由甲羟戊酸合成异戊烯基焦磷酸。因此,异恶草酮对由甲羟戊酸合成香叶基香叶基焦磷酸没有直接的体外作用。大豆和苘麻的绿化幼苗均能代谢异恶草酮。在大豆和苘麻之间未检测到代谢产物的定性差异。因此,异恶草酮不太可能通过代谢为抑制类萜合成的有毒化学物质而产生差异作用。异恶草酮要么具有尚未确定的作用模式,要么具有一种选择性代谢产物,即它在敏感物种中比在耐受物种中活性高得多。

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