Biochemical and molecular mechanisms of diafenthiuron resistance in the whitefly,Bemisia tabaci

B-biotype Bemisia tabaci has developed high levels of resistance to many insecticides. To investigate the risks and explore possible mechanisms of resistance to diafenthiuron in B. tabaci, a 32.8-fold diafenthiuron-resistant strain (R-DfWf) was established after selection for 36 generations compared with the susceptible strain (S-Lab). Biochemical assays showed that the activity of cytochrome P450 towards p-NA was significantly higher (4.37-fold higher) in the R-DfWf strain than in the S-Lab strain. Similarly, the carboxylesterase (COE) activity and glutathione S-transferase (GST) activity were also significantly higher (3.12- and 1.83-fold higher, respectively) in the R-DfWf strain than in the S-Lab strain. The expression of five of seven P450 genes was significantly higher (>3-fold) in the R-DfWf strain than in the S-Lab strain. The expression of COE2 was significantly higher (>2.5-fold) in the R-DfWf than in the S-Lab strain. The expression of GST and GST2 was significantly higher (>2.3-fold) in the R-DfWf than in the S-Lab. Thus, cytochrome P450, COE and GST may appear to be responsible for the resistance to diafenthiuron in B. tabaci. It is also valuable for usage of insecticides for resistance management and control of this species.     

日本看麦娘对高效氟吡甲禾灵代谢抗性的初步研究

为了明确日本看麦娘对高效氟吡甲禾灵(haloxyfop-R-methyl)的代谢抗性机理,研究了抗性和敏感生物型体内细胞色素P450还原酶(cytochrome P-450 monooxygenases,P450)和谷胱甘肽-S-转移酶(glutathione-S-transferases,GSTs)的活性差异。结果表明,未用药剂处理时,抗性日本看麦娘P450与GSTs的活性均高于敏感日本看麦娘。高效氟吡甲禾灵茎叶喷雾处理2 d后,敏感植株反应剧烈,P450与GSTs活性均呈现急剧的变化趋势,而抗性种群的变化趋势平缓。处理后第6 d,敏感种群较抗性种群先出现下降趋势,其活性也明显低于抗性种群。处理后第10 d活性均降到最低,并且依然低于施药初期。从而可以得出:高效氟吡甲禾灵被抗性日本看麦娘体内的细胞色素P450还原酶催化,经过羟化作用迅速解毒,并在GSTs的催化下形成了无毒或低毒的化合物,使其免受伤害。表明代谢酶活性增强是日本看麦娘对高效氟吡甲禾灵产生抗性的机理之一。     

靶标酶在除草剂研究与开发中的作用

大多数除草剂都是通过特殊酶的抑制而产生杀草作用的。根据作用靶标对除草剂进行分类,了解靶标酶的作用机理及特性,对于新型除草剂的设计和杂草抗性的防治能够起到很大的帮助。本文介绍了谷胱甘肽转移酶(GST)、细胞色素P450酶、乙酰乳酸合成酶(ALS)、乙酞辅酶A羧化酶(ACCace)的研究进展。并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。     

棉铃虫微粒体多功能氧化酶系组分含量及酶活性在不同生长发育阶段的变化规律研究

细胞色素 P4 50和细胞色素 b5在 KQR和 HDS种群棉铃虫的不同生长发育阶段含量不同 ,但变化规律大致相似 ,均是在 3龄期含量较低 ,从 3龄到 6龄含量上升并达到最高值 ,然后含量逐渐下降 ,直到蛹期达最低值。单加氧酶 MROD和 ECOD在 KQR种群棉铃虫不同生长发育阶段活性大小不同 ,而且变化规律明显不同。从 3龄到 6龄期间 ,MROD活性呈上升趋势 ,并在 6龄期达到最大 ,之后活性逐渐下降 ,在蛹和成虫阶段活性达最小 ;而 ECOD活性在不同生长发育阶段间的差异则不是很大 ,没有明显的阶段表达特异性     

淡紫灰链霉菌株xjy活性产物的抑菌作用及对蔬菜病害的防治效果

拮抗性微生物是生物农药的重要来源之一,加强拮抗菌的应用基础研究对于发展生物农药具有促进作用.在植物病害生物防治中拮抗性微生物主要是链霉菌属及其相关类群[1].     

除草剂安全剂的生理生化作用机制研究进展

除草剂安全剂是一种化学物质,它可以通过生理或生化的途径降低除草剂对作物的毒性,而不降低除草剂的功效.安全剂影响作物的吸收和传导,诱导作物体内P450酶活性、谷胱甘肽调控及其靶标酶ALS的活性.其生理和生化机制研究,不仅有助于安全剂的开发和优化,同时也是了解和运用除草剂活性和抗性机制的途径.该文综述了近年来国内外安全剂生理生化作用机制的研究进展,并探讨其研究方向.     

细胞色素P450s的纯化与鉴定

综述了细胞色素 P450s纯化和鉴定技术的研究进展。纯化技术包括色谱、电泳和基因克隆技术 ;鉴定方法有光谱测定、酶活测定、电泳分析和蛋白质印迹测定。     

The basis for the safening of clomazone by phorate insecticide in cotton and inhibitors of cytochrome P450s

Clomazone may be safely used in cotton to manage weeds when applied following treatments of the organophosphate insecticides phorate or disulfoton. The loss of chlorophyll and carotenoids with 6 days of 100 nM clomazone treatment of cotton seedlings was partially prevented with phorate in hydroponic solution in a rate-dependent manner. In a study to examine the timing of safening from a one-day clomazone (100 nM) treatment, maximum safening was achieved when phorate (50 μM) was applied the same day as clomazone. Phorate decreased metabolism of ¹⁴C-clomazone to polar metabolites in excised cotton shoots and shoots of intact cotton plants. Microsomal studies of corn shoots showed an NADPH-dependent/cytochrome P450 reaction was inhibited by phorate. Additional studies with corn microsomes, corn seedlings and cotton seedlings supported the basis of clomazone safening is the inhibition of toxic clomazone metabolism by P450 inhibitors.     

聚乙二醇8000对棉铃虫微粒体蛋白沉淀作用的研究

为建立棉铃虫Helicoverpa armigera微粒体P450的分离纯化方案,比较了不同浓度下聚乙二醇8000(PEG8000)对棉铃虫幼虫中肠和脂肪体微粒体蛋白的沉淀作用。结果表明,终浓度为8.0×104 mg/L的PEG8000可以使中肠和脂肪体微粒体蛋白的78%沉淀下来,其中包含的细胞色素P450分别占中肠和脂肪体P450总量的28%和34%。SDS-PAGE显示,中肠微粒体经8.0×104 mg/L的PEG8000沉淀后,被沉淀蛋白的分子质量主要集中在14.1 ~ 40 kD和66 ~97 kD范围内。     

细胞色素P450s酶系催化除草剂代谢的研究进展

综述了细胞色素P450s酶系催化的单加氧反应机理,细胞色素P450s酶系在酰胺类、三氮苯类、磺酰脲类、脲类、苯氧羧酸类等除草剂的活性或降解代谢中的催化反应。讨论了研究细胞色素P450s酶系代谢作用在除草剂选择性、抗药性机理,抗除草剂作物的培育以及除草剂安全剂的解毒机理等方面的意义。     

Biotransformation of s-Triazine Herbicides and Related Degradation Products in Liquid Cultures by the White Rot Fungus Phanerochaete chrysosporium

The ability of the white rot basidiomycete Phanerochaete chrysosporium to transform s-triazine herbicides has been investigated in laboratory experiments. The chlorinated metabolites formed during atrazine N-dealkylations were not further transformed by the fungus, whereas hydroxy-atrazine was converted to an unknown product. P. chrysosporium was also able to carry out the N-dealkylation of the herbicides simazine, propazine and terbuthylazine. Herbicide metabolism was not supported by purified peroxidases. The highest rates of herbicide N-dealkylation were obtained in liquid cultures maintained under moderate temperature allowing a long mycelium growing phase. Atrazine transformation was found to be supported by the mycelium, which contained significant amounts of microsomal cytochrome P450. Herbicide N-dealkylation was decreased in the presence of 1-aminobenzotriazole, in agreement with the involvement of P450 monooxygenases in atrazine metabolism. © 1997 SCI.     

新烟碱类杀虫剂吡虫啉和噻虫嗪的代谢研究进展

对新烟碱类杀虫剂吡虫啉和噻虫嗪的化学结构特点及代谢研究进展进行了综述,重点对其在哺乳动物、植物和昆虫体内的代谢途径及相关的生物代谢酶进行了阐述。吡虫啉和噻虫嗪在环境中可被动物、植物、微生物及昆虫所代谢,与其生物代谢相关的酶主要是微粒体细胞色素P450同工酶和醛氧化酶,其中,P450同工酶可催化吡虫啉和噻虫嗪发生羟基化、去饱和、脱烷基、硝基还原等代谢反应,而醛氧化酶主要催化其硝基部分的还原。吡虫啉和噻虫嗪经过代谢后其生物活性通常有所降低,但也有部分代谢产物的活性反而升高,增加了其对昆虫的毒性以及对非靶标生物的风险。明确吡虫啉和噻虫嗪的代谢途径、代谢产物及其生物活性,对于了解新烟碱类杀虫剂的代谢机理,以及安全有效地使用该类杀虫剂具有重要意义。     

吡唑解草酯对小麦细胞色素P450的诱导作用及其光谱特征

用吡唑解草酯浇灌小麦,试验结果表明,50μmol/L吡唑解草酯处理抗6号小麦,可使其细胞色素P450含量达到最大值108.18 pmol/mg蛋白质,为对照组的1.67倍;100μmol/L吡唑解草酯处理敏18号小麦,可使其细胞色素P450含量达到最大值80.97 pmol/mg蛋白质,为对照组的1.86倍。吡唑解草酯对两个小麦品种的细胞色素P450均有诱导作用,抗6号小麦更容易被诱导,这与两小麦品种的耐药性一致。室温(20±1)℃下扫描不同时间的细胞色素P450-CO结合光谱,结果表明,微粒体粗提液室温(20±1)℃保存200 min后,细胞色素P450完全转变为细胞色素P420。     

北京、山东和湖南地区烟粉虱抗药性及CYP4v2和CYP6CX1 mRNA水平表达量分析

于2011年采集北京、山东和湖南三地的烟粉虱,进行B、Q隐种鉴定,并测定4种杀虫剂的抗药性,同时通过荧光定量PCR分析CYP4v2和CYP6CX1两个基因的mRNA水平的表达量。结果表明,北京、湖南和长沙烟粉虱均为Q隐种。抗药性监测表明,北京和湖南种群对阿维菌素敏感,山东种群抗性水平较低,而对烟碱类药剂噻虫嗪出现不同程度的抗药性,其中湖南地区烟粉虱对噻虫嗪的抗药性达到49.08倍的高抗水平,北京和山东地区也达到中抗水平。另外,这3个地区的种群对毒死蜱和联苯菊酯抗性水平都较低。通过qRT-PCR分析三地的CYP4v2和CYP6CX1基因表达量,发现相对于敏感种群CYP4v2基因在北京、山东和湖南3个地理种群中分别过量表达3.85倍、19.57倍和10.78倍,而CYP6CX1基因在北京种群中过量表达20.55倍。结果提示田间烟粉虱的细胞色素P450基因CYP4v2和CYP6CX1过量表达可能会是烟粉虱抗药性的形成机制之一。     

Synergistic and antagonistic effects of atrazine on the toxicity of organophosphorodithioate and organophosphorothioate insecticides to Chironomus tentans (Diptera: Chironomidae)

The acute toxicities of two organophosphorodithioate (dimethoate and disulfoton) and two organophosphorothioate (omethoate and demeton-S-methyl) insecticides were evaluated individually and in binary combination with the herbicide atrazine using fourth-instar larvae of the aquatic midge, Chironomus tentans. Atrazine alone up to 1000 μg/L did not show significant toxicity to the midges in a 48-h bioassay. However, atrazine concentrations as low as 1 μg/L in combination with dimethoate at EC₂₅ (concentration to affect 25% of tested midges), 100 μg/L in combination with disulfoton (EC₂₅), and 10 μg/L in combination with demeton-S-methyl (EC₂₅) significantly enhanced the toxicity of each organophosphate insecticide. In contrast, atrazine concentrations of 10 μg/L and above in combination with omethoate (EC₂₅) significantly decreased the toxicity of the insecticide. Biochemical analysis indicated that increased toxicity of dimethoate, disulfoton, and demeton-S-methyl in binary combination with atrazine correlated to the increased inhibition of acetylcholinesterase. Furthermore, cytochrome P450-dependent O-deethylation activity in the midges exposed to atrazine at 1000 μg/L was 1.5-fold higher than that in the control midges. Thus, atrazine appeared to induce cytochrome P450 monooxygenases in the midges. Elevated cytochrome P450 monooxygenase activity may increase the toxicities of dimethoate, disulfoton, and demeton-S-methyl by enhancing the oxidative activation of dimethoate into omethoate, and disulfoton and demeton-S-methyl into their sulfoxide analogs with increased anticholinesterase activity. In contrast, atrazine reduced the toxicity of omethoate possibly by enhancing the oxidative metabolic detoxification since omethoate does not require oxidative activation.