Molecular characterisation of resistance to ALS-inhibiting herbicides in Hordeum leporinum biotypes

被引:57
作者
Yu, Qin [1 ]
Nelson, Jared K.
Zheng, Ming Q.
Jackson, Michael
Powles, Stephen B.
机构
[1] Univ Western Australia, Sch Plant Biol, Western Australian Herbicide Resistance Initiat, Crawley, WA 6009, Australia
[2] China Agr Univ, Dept Appl Chem, Beijing 100094, Peoples R China
[3] Nufarm Australia Ltd, Kwinana, WA 6167, Australia
关键词
acetolactate synthase; Hordeum leporium; herbicide resistance; target-site mutation;
D O I
10.1002/ps.1429
中图分类号
S3 [农学(农艺学)];
学科分类号
0901 ;
摘要
BACKGROUND: The acetolactate synthase (ALS)-inhibiting herbicide sulfosulfuron is registered in Australia for the selective control of Hordeum leporinum Link. in wheat crops. This herbicide failed to control H. leporinum on two farms in Western Australia on its first use. This study aimed to determine the level of resistance of three H. leporinum biotypes, identify the biochemical and molecular basis and develop molecular markers for diagnostic analysis of the resistance. RESULTS: Dose-response studies revealed very high level (>340-fold) resistance to the sulfonylurea herbicides sulfosulfuron and sulfometuron. In vitro ALS assays revealed that resistance was due to reduced sensitivity of the ALS enzyme to herbicide inhibition. This altered ALS sensitivity in the resistant biotypes was found to be due to a mutation in the ALS gene resulting in amino acid proline to serine substitution at position 197. In addition, two- to threefold higher ALS activities were consistently found in the resistant biotypes, compared with the known susceptible biotype. Two cleaved amplified polymorphic sequence (CAPS) markers were developed for diagnostic testing of the resistant populations. CONCLUSION: This study established the first documented case of evolved ALS inhibitor resistance in H. leporinum and revealed that the molecular basis of resistance is due to a Pro to Ser mutation in the ALS gene. (C) 2007 Society of Chemical Industry.
引用
收藏
页码:918 / 927
页数:10
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