细胞色素P450酶系与植物的化学防御

简述了植物细胞色素P450酶系(P450s)在植物防御性物质的合成以及对除草剂等外源化学物质的解毒方面的功能,提出了利用分子生物学等技术,分离人们需要的P450基因,并在转基因植物中得到表达,培育出具有抗病虫、除草剂等功能的转基因作物的展望。     

除草剂安全剂对作物细胞色素P450及其他酶活性和水平的影响

综述了除草剂安全剂对作物中参与除草剂解毒作用的酶以及作为除草剂作用靶标位点酶水平与活性的影响。安全剂能增强细胞色素P450酶系统活性,诱导P450在除草剂降解中的作用;增加作物体内谷胱甘肽的含量,从而促进除草剂与谷胱甘肽的轭合而发挥解毒作用;降低由于除草剂对乙酰乳酸合成酶的抑制作用而引起的植物毒性等。     

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。     

抗阿维菌素小菜蛾的细胞色素P450酶系研究

通过对不同发育时期敏感和抗阿维菌素小菜蛾品系细胞色素P450含量的测定,以及使用不同模式底物对P450单加氧酶活性的比较研究发现:除成虫期外,不同发育时期抗性品系小菜蛾中P450和细胞色素b5的含量都高于敏感品系;抗性品系还原型辅酶Ⅱ(NADPH)-细胞色素P450还原酶活性是敏感品系的1.97倍;同时发现抗性品系中甲氧试卤灵-O-脱甲基酶(MROD)、乙氧试卤灵-O-脱乙基酶(EROD)、乙氧基香豆素-O-脱乙基酶(ECOD)以及对硝基苯甲醚-O-脱甲基酶(PNOD)的活性均明显高于敏感品系,分别为敏感品系的9.41、4.15、1.67和2.94倍。研究结果表明,细胞色素P450含量和单加氧酶活性的增高是小菜蛾对阿维菌素产生抗性的一个重要机制。     

有机磷类杀虫剂代谢机制研究进展

文章对有机磷类杀虫剂代谢机制的研究进展以及昆虫对此类杀虫剂的相关代谢抗性机制进行了总结,阐述了有机磷杀虫剂的生物代谢途径及相关代谢酶系。在生物体中,有机磷类杀虫剂主要发生氧化代谢、水解代谢和轭合代谢等反应。其氧化代谢主要在细胞色素P450酶系(P450s)的催化作用下进行,其中,最重要的氧化反应是硫代有机磷酸酯类杀虫剂氧化脱硫形成生物毒性更高的有机磷氧化物的反应,以及氧化脱芳(烷)基化的反应;有机磷杀虫剂及其氧化产物在生物体内还可发生水解代谢反应,在对氧磷酶PON1等磷酸三酯酶的催化作用下,水解生成低毒性或者无毒的代谢物;有机磷杀虫剂的轭合代谢主要是在谷胱甘肽硫转移酶(GSTs)的催化下进行的。昆虫对有机磷类杀虫剂的代谢抗性与昆虫中参与此类杀虫剂代谢的解毒酶的改变密切相关,其中,与有机磷类杀虫剂代谢相关的P450s基因的过量表达和酶活性增强、丝氨酸水解酯酶的过量表达及基因突变、GSTs基因的过量表达等,均可导致铜绿蝇Lucilia cuprina、桃蚜Myzus persicae等昆虫对二嗪磷和马拉硫磷等有机磷类杀虫剂的代谢抗性。明确有机磷类杀虫剂的结构特点、代谢途径以及昆虫对此类杀虫剂的代谢抗性机制,对掌握有机磷类杀虫剂的毒理学机制,安全有效地使用此类杀虫剂,有效治理害虫对有机磷类杀虫剂的抗药性,以及开发生物选择性好的新型有机磷类杀虫剂,均具有重要意义。     

多功能氧化酶系与甜菜夜蛾对氯氟氰菊酯抗药性的关系

比较了甜菜夜蛾Spodoptera exigua (Hübner)抗氯氟氰菊酯品系和敏感品系5龄幼虫中肠、脂肪体及体壁微粒体细胞色素P450的含量,结果表明,抗性和敏感品系不同组织细胞色素P450的含量均为中肠＞脂肪体＞体壁,抗性品系中肠、脂肪体及体壁细胞色素P450的含量分别是敏感品系的1.78、1.54及1.37倍。中肠微粒体甲氧试卤灵-O-脱甲基酶、乙氧试卤灵-O-脱乙基酶、乙氧香豆素-O-脱乙基酶、芳香基羟基化酶及艾氏剂环氧化酶的活性测定结果表明,抗性品系中肠5种酶的活性分别比敏感品系的酶活性提高1.33、1.73、1.40、1.51及1.30倍,说明甜菜夜蛾对氯氟氰菊酯的抗药性与微粒体多功能氧化酶活性的提高密切相关。     

三唑并嘧啶磺酰胺类除草剂的研究概况

三唑并嘧啶磺酰胺类除草剂是将磺酰脲类除草剂通过脲桥的结构改造和修饰而得,它既保持了磺酰脲类除草剂的超高效性,又克服了一些磺酰脲类除草剂品种在土壤中残留期较长、易对后茬作物造成伤害等缺点。本文综述了三唑并嘧啶磺酰胺类除草剂的结构、主要品种、作用机理、应用研究和发展前景。     

细胞色素P450抑制剂对白腐菌Phlebia lindtneri降解氯丹的影响

为确定细胞色素P450酶系在白腐菌Phlebia lindtneri降解有机氯类农药氯丹中的作用,在液体培养条件下,以胡椒基丁醚和1-氨基苯并三唑作为细胞色素P450的抑制剂,分析了不同浓度抑制剂对氯丹的降解、代谢产物的生成以及中间代谢物降解的影响。结果表明:与对照相比,高浓度(1.0 mmol/L)胡椒基丁醚或1-氨基苯并三唑处理15 d后氯丹的降解率均下降了约60%,且其代谢产物中除七氯和二氯代六氯的检出量显著增加外,其余环氧化及羟基化代谢产物均未检出;此外,添加高浓度的抑制剂可导致白腐菌降解中间代谢产物七氯及二氯代六氯的降解率下降90%以上,氧化氯丹的降解率下降70%以上,但不影响环氧七氯的降解。表明细胞色素P450可能是氯丹降解的主要酶系,其参与催化了氯丹的初始羟基化和水解、七氯和二氯代六氯的环氧化及氧化氯丹的水解等多个反应过程。     

磺酰脲类除草剂的微生物降解研究进展

磺酰脲类除草剂是使用最广泛的除草剂之一。微生物降解是磺酰脲类除草剂在土壤中降解的重要方式。本文简要概述了土壤微生物对磺酰脲类除草剂的降解、降解机理及影响微生物降解磺酰脲类除草剂的因素。     

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。     

Identification of cytochrome P450 differentiated expression related to developmental stages in bromadiolone resistance in rats (Rattus norvegicus)

Adult, 20-week-old, rats from a Danish bromadiolone-resistant strain of rats (Rattus norvegicus) over-express the cytochrome P450 genes Cyp2e1, Cyp3a2 and Cyp3a3 upon bromadiolone exposure. Furthermore, adult female rats of this strain over-express the Cyp2c13 gene and suppress Cyp2c12, while males over-express the Cyp2a1 gene. The altered gene expression has been suggested to be involved in the bromadiolone resistance by facilitating enhanced anticoagulant metabolism. To investigate the gene expression of these cytochrome P450 genes in rats of different developmental stages we compared expression profiles from 8-, 12- and 20-week-old resistant rats of the Danish strain to profiles of anticoagulant-susceptible rats of same ages. The three age-groups were selected to represent a group of pre-pubertal, pubertal and adult rats. We found expression profiles of the pre-pubertal and pubertal resistant rats to concur with profiles of the adults suggesting that cytochrome P450 enzymes are involved in the Danish bromadiolone resistance regardless of developmental stage. We also investigated the relative importance of the six cytochrome P450s in the different development stages of the resistant rats. The P450-3a2 and -3a3 isoforms were proposed to be of higher importance in adult male resistance than in pre-pubertal resistance. In contrast, the P450-2c13 and -3a2 isoforms were proposed to be more important in sexual immature female resistance, while the P450-2e1 and -3a3 isoforms were suggested to play a more significant role in adult female resistance.     

昆虫细胞色素P450基因的表达与调控及P450介导抗性的分子机制

本文综述了在杀虫剂抗性中起重要作用的 P4 50酶系研究的最新进展。内容包括 :细胞色素 P4 50酶系基因及其基因的表达与调控 ,P4 50介导抗性的分子基础。细胞色素 P4 50表达表现出发育期、组织、品系特异性及可诱导性。 P4 50表达的调控机制复杂 ,可能受顺式调控元件 (如 CYP6 B1)或反式作用因子 (如CYP6 A1)或顺式、反式因子的共同调控 (如 CYP6 D1)。调控可能涉及转录增强的转录机制或 m RNA稳定性增加的转录后机制。 P4 50的超量表达是 P4 50酶系介导抗性的主要机制 ,P4 50的氨基酸替换也可能在杀虫剂抗性中起作用。     

基于转录组测序技术分析吡虫啉或氟啶虫胺腈对麦二叉蚜细胞色素P450基因表达的影响

为了筛选出麦二叉蚜Schizaphis graminum 参与吡虫啉或氟啶虫胺腈代谢调节的细胞色素P450(P450) 基因,采用浸渍法,用吡虫啉或氟啶虫胺腈处理麦二叉蚜24 h后,通过构建转录组测序文库,并进行RNA-seq测序,筛选出差异性表达的P450基因,并进行实时荧光定量PCR(qPCR) 验证。结果表明:用吡虫啉处理麦二叉蚜后,有19个P450基因上调表达,15个P450基因下调表达;用氟啶虫胺腈处理麦二叉蚜后,有18个P450基因上调表达,15个P450基因下调表达。运用qPCR验证了吡虫啉对12个P450基因的诱导表达,其结果与DGE测序文库显示的结果基本一致。这些结果可为深入研究麦二叉蚜P450对蚍虫啉和氟啶虫胺腈的解毒代谢作用提供依据。     

The role of cytochrome P450 monooxygenase in the different responses to fenoxaprop-P-ethyl in annual bluegrass (Poa annua L.) and short awned foxtail (Alopecurus aequalis Sobol.)

Herbicide resistance or tolerance in weeds mediated by cytochrome P450 monooxygenase is a considerable problem. However, cytochrome P450 mediated resistance or tolerance in weeds was less studied. Thus, in this work, the role of the cytochrome P450 monooxygenase in the different responses of Poa annua and Alopecurus aequalis to fenoxaprop-P-ethyl was studied. We found that the effect of fenoxaprop-P-ethyl could be synergized by piperonyl butoxide (PBO) in P. annua, but not by malathion. After being treated with fenoxaprop-P-ethyl (containing mefenpyr-diethyl), the contents of cytochrome P450 and cytochrome b₅ in P. annua increased significantly compared to plants treated with mefenpyr-diethyl only or untreated plants. However, the increase was less in A. aequalis, which was susceptible to fenoxaprop-P-ethyl. The activities of ρ-nitroanisole O-demethylase (PNOD), ethoxyresorufin O-deethylase (EROD), ethoxycoumarin oxidase (ECOD) and NADPH-dependent cytochrome P450 reductase mediated by cytochrome P450 monooxygenase increased in P. annua after treatment with fenoxaprop-P-ethyl, especially the activities of ECOD and cytochrome P450 reductase. Besides this, cytochrome P450 monooxygenase activity toward fenoxaprop-P-ethyl in P. annua increased significantly compared to untreated or treated with mefenpyr-diethyl plants and treated or untreated A. aequalis. Cytochrome P450 monooxygenase may play an important role in the different responses to fenoxaprop-P-ethyl in P. annua and A. aequalis.     

In-vivo effects of 2,4-D and atrazine on cytochrome P-450 and insecticide toxicity in southern armyworm (Spodoptera eridania) larvae

After feeding 2,4-D or atrazine in a diet to southern armyworm (Spodoptera eridania Cram.) larvae for three days, the effect on total content and activities of cytochrome P450 and on insecticide toxicity were determined. Both 2,4-D and atrazine induced cytochrome P450-catalyzed aldrin epoxidation (AE) and methoxyresorufin O-demethylatin (MROD). The 2,4-D was a more potent inducer for total cytochrome P450 content, whereas atrazine disproportionately increased AE. Both compounds increased MROD significantly. The apparent kinetic characteristics of AE indicates that 2,4-D and atrazine induced similar P450 isozymes (K_m 8.78 and 7.80 μM, respectively), which may differ from the constitutive isozyme (K_m 3.14 μM). The 2,4-D-induced cytochrome P450 contributed to decreased carbaryl and permethrin toxicity, whereas the atrazine-induced cytochrome P450 caused decreased parathion and permethrin toxicity. The carbaryl toxicity correlated directly with 2,4-D-induced total P450 content and activities but not with atrazine-induced changes. The 2,4-D and atrazine also induced nonspecific esterase activity which may contribute to permethrin detoxification.     

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。     

Expression of a wheat cytochrome P450 monooxygenase in yeast and its inhibition by glyphosate

Glyphosate is a non-selective herbicide which acts by inhibiting 5-enolpyruvylshikimate-3-phosphate synthase. Wheat cytochrome P450 monooxygenase specifically catalyzes the metabolism of some sulfonylurea herbicides such as chlorsulfuron and triasulfuron. Here we report that glyphosate is an inhibitor of a wheat cytochrome (CYP71C6v1), the cDNA of which was amplified by RT-PCR and heterologously expressed in yeast. The microsomal fractions derived from this strain had a Soret peak at 502 nm in the reduced carbon monoxide difference spectrum, which is a typical spectral characteristic. The addition of glyphosate to the microsomal protein resulted in a Type II spectrum indicative of binding via the nitrogen group to haem of cytochrome P450 as a sixth ligand. A spectral dissociation constant, K(s) of 70 micromol litre(-1) was observed and an IC50 of 11 micromol litre(-1) was found for glyphosate inhibition of CYP71C6v1 P450 activity.