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31.
乙酰辅酶A羧化酶抑制剂的构效关系和抗性研究进展   总被引:1,自引:0,他引:1  
衣克寒  付颖  叶非 《植物保护》2012,38(1):11-17
乙酰辅酶A羧化酶(ACCase)抑制剂是以乙酰辅酶A羧化酶为作用靶标的一类除草剂.这类除草剂通过抑制真核型乙酰辅酶A生成丙二酰辅酶A的羧化反应,进而抑制植物脂肪酸的合成,多用于苗后有选择性地防除一年生禾本科杂草.本文综述了该类除草剂的作用机理、构效关系及在应用中的抗性研究进展.  相似文献   
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BACKGROUND: Target‐site resistance is the major cause of herbicide resistance to acetolactate synthase (ALS)‐ and acetyl‐CoA carboxylase (ACCase)‐inhibiting herbicides in arable weeds, whereas non‐target‐site resistance is rarely reported. In the Echinochloa phyllopogon biotypes resistant to these herbicides, target‐site resistance has not been reported, and non‐target‐site resistance is assumed to be the basis for resistance. To explore why target‐site resistance had not occurred, the target‐site genes for these herbicides were isolated from E. phyllopogon, and their expression levels in a resistant biotype were determined. RESULTS: Two complete ALS genes and the carboxyltransferase domain of four ACCase genes were isolated. The expression levels of ALS and ACCase genes were higher in organs containing metabolically active meristems, except for ACC4, which was not expressed in any organ. The differential expression among examined organs was more prominent for ALS2 and ACC2 and less evident for ALS1, ACC1 and ACC3. CONCLUSION: E. phyllopogon has multiple copies of the ALS and ACCase genes, and different expression patterns were observed among the copies. The existence of three active ACCase genes and the difference in their relative expression levels could influence the occurrence of target‐site resistance to ACCase inhibitors in E. phyllopogon. Copyright © 2012 Society of Chemical Industry  相似文献   
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BACKGROUND: The repeated use of acetyl‐coenzyme A carboxylase (ACCase) inhibiting herbicides to control grass weeds has selected for resistance in Lolium spp. populations in Italy. The efficacy of pinoxaden, a recently marketed phenylpyrazoline herbicide, is of concern where resistance to ACCase inhibitors has already been ascertained. ACCase mutations associated with pinoxaden resistance were investigated, and the cross‐resistance pattern to clodinafop, haloxyfop, sethoxydim, clethodim and pinoxaden was established on homo/heterozygous plants for four mutant ACCase alleles. RESULTS: Seven different mutant ACCase alleles (1781‐Leu, 1999‐Leu, 2041‐Asn, 2041‐Val, 2078‐Gly, 2088‐Arg and 2096‐Ala) and 13 combinations with two types of mutation were detected in the pinoxaden‐resistant plants. The 1781‐Leu allele appears to confer a dominant resistance to pinoxaden, clodinafop, haloxyfop, sethoxydim and clethodim at 60 g AI ha?1. The 2041‐Asn and 2041‐Val alleles are associated with dominant or partially dominant resistance to FOPs, no substantial resistance to DIMs and a moderate resistance to pinoxaden. The 2088‐Arg allele endows a partially dominant resistance to clodinafop, sethoxydim and most likely to pinoxaden. In addition, non‐target‐site resistance mechanisms seem to be involved in pinoxaden resistance. CONCLUSION: Almost all the ACCase mutations selected in the field by other ACCase inhibitors are likely to confer resistance to pinoxaden. Although pinoxaden is sometimes able to control FOP‐resistant populations, it should not be considered as a sustainable ACCase resistance management tool. The presence of non‐ACCase‐based resistance mechanisms that could confer resistance to herbicides with different modes of action further complicates the resistance management strategies. Copyright © 2011 Society of Chemical Industry  相似文献   
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八种除草剂对小麦田三种抗精噁唑禾草灵杂草的生物活性   总被引:3,自引:0,他引:3  
为筛选能有效防除抗精噁唑禾草灵杂草的除草剂,采用温室盆栽法测定菵草(敏感S_w、抗性R_w)、日本看麦娘(敏感S_r、抗性R_r)、耿氏硬草(敏感S_y、抗性R_y)对精噁唑禾草灵的抗性水平,并研究了8种除草剂对这3种抗性杂草的生物活性。结果显示,3种杂草抗性种群对精噁唑禾草灵的抗性指数均大于33.7,已达高抗水平。3种杂草抗性种群均对同类乙酰辅酶A羧化酶类抑制剂唑啉草酯和炔草酯产生了11.6~56.5倍不等的高水平抗性。对部分乙酰乳酸合成酶类抑制剂产生了2.0~4.8倍的低水平抗性,氟唑磺隆对3种杂草抗性种群防效较差,GR_(90)为67.31~114.39g(a.i.)/hm~2;啶磺草胺仅对Rr种群防效较好,GR_(90)为4.67 g(a.i.)/hm~2;甲基二磺隆对3种杂草抗性种群防效均较好,但对Rr种群存在抗性风险,已出现2.0倍低水平抗性;磺酰磺隆对Ry和Rr种群防效较好;丙苯磺隆对Rr种群防效好。细胞分裂抑制剂氟噻草胺对3种杂草抗性种群防效均最好,在田间推荐剂量120 g(a.i.)/hm~2下可达90%以上的防效。  相似文献   
36.
为了解安全剂双苯恶唑酸缓解除草剂精恶唑禾草灵对水稻药害的效果,通过温室水培和盆栽法研究双苯恶唑酸对水稻精恶唑禾草灵药害的解毒效果,并对其解毒机制进行初步探讨。结果表明:水稻萌发期,粳稻和籼稻在0.25、0.5、1μg/m L精恶唑禾草灵处理下,解毒效果最好的安全剂添加比例分别为1∶1、1∶5、1∶5,粳稻株高、胚根长的抑制率比精恶唑禾草灵单独使用分别降低18.07、37.50,26.56、34.94,41.30、37.50个百分点,籼稻株高、胚根长的抑制率分别降低23.31、42.33,27.22、34.91,46.76、31.14个百分点;水稻两至三叶期,粳稻和籼稻在25、100μg/m L精恶唑禾草灵处理下,谷胱甘肽-S-转移酶(GST)和乙酰辅酶A羧化酶(ACCase)活性最高的安全剂添加比例均为1∶1,此时粳稻的GST活性和ACCase活性比精恶唑禾草灵单独使用分别增加42.21%和65.63%、46.72%和140.43%,籼稻的GST活性和ACCase活性比精恶唑禾草灵单独使用分别增加52.18%和105.71%、55.55%和169.52%。安全剂双苯恶唑酸提高了精恶唑禾草灵处理后水稻幼苗中GST、ACCase活性,减轻了精恶唑禾草灵对水稻的伤害,为水稻生产中通过添加双苯恶唑酸降低精恶唑禾草灵对水稻的药害提供了依据。  相似文献   
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The mechanisms of herbicide resistance were investigated in two diclofop-methyl-resistant Lolium spp. populations from central Italy, Roma '94 and Tuscania '97. These two populations were compared with two susceptible Italian populations (Vetralla '94, Tarquinia '97) and a resistant and a susceptible population from Australia, SLR31 and VLR1. The activity of acetyl Co-A carboxylase (ACCase) extracted from susceptible (S) or resistant (R) individuals from the Italian populations was inhibited by both aryloxyphenoxypropanoate (diclofop acid and fluazifop acid) and cyclohexanedione (sethoxydim) herbicides. Diclofop-methyl was rapidly de-esterified to diclofop acid at a similar rate in both R and S populations. In all populations, diclofop acid was subsequently degraded to other metabolites. The rate of degradation of diclofop acid was not significantly faster in R than in S populations; however, diclofop acid was degraded more completely in Roma '94 and Tuscania '97 compared with the S populations. Application of the mixed-function oxidase inhibitor 1-aminobenzotriazole (ABT) significantly enhanced diclofop-methyl toxicity towards both R populations, but not in S populations. However, enhanced herbicide metabolism does not completely account for the measured resistance level. A mechanism other than an altered ACCase and enhanced herbicide metabolism appears to be responsible for resistance to diclofop-methyl in Roma '94 and Tuscania '97.  相似文献   
39.
几种除草剂靶酶及其抑制剂的研究进展   总被引:1,自引:0,他引:1  
根据作用靶标对除草剂进行分类,对于新型除草剂的设计能够起到很大的帮助。迄今为止,人们已发现除草剂的不同作用位点近30种,涉及到50余种不同化学结构的化合物。文中介绍了谷氨酰胺合成酶(GS)、咪唑甘油磷酯脱水酶(IGPD)、乙酰辅酶A羧化酶(ACCace)、八氢番茄红素脱氢酶(PDS)及其各自抑制剂的研究进展。分别从酶的生理功能、酶学特征、抑制剂作用机理、抑制剂的研究、抗性等方面进行了不同程度的阐述。  相似文献   
40.
为明确河南省部分地区的多花黑麦草Lolium multiflorum种群对乙酰辅酶A羧化酶(acetylCoA carboxylase,ACCase)和乙酰乳酸合成酶(acetolactate synthase,ALS)抑制剂类除草剂的抗性水平和抗性机理,采用整株生物测定法测定采自新乡市和驻马店市的多花黑麦草种群对ACCase抑制剂类除草剂精噁唑禾草灵、炔草酯、唑啉草酯和ALS抑制剂类除草剂甲基二磺隆、氟唑磺隆、啶磺草胺的抗性水平,并对多花黑麦草ACCase和ALS靶标酶编码基因进行克隆及氨基酸序列比对,分析其靶标抗性机理。结果显示,与多花黑麦草敏感种群HNXX01相比,HNZMD04和HNXX05种群对6种除草剂均产生了抗性,HNZMD04种群对精噁唑禾草灵和啶磺草胺的相对抗性倍数分别为44.65和40.31,对炔草酯和氟唑磺隆的相对抗性倍数分别为11.91和11.93;HNXX05种群对精噁唑禾草灵和氟唑磺隆的相对抗性倍数分别为27.70和25.67。HNZMD04和HNXX05抗性种群的ACCase基因均发生了D2078G突变,2个种群的突变率分别为55%和70%;HNZMD04...  相似文献   
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