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1.
为明确以天然产物阿魏酸为母体进行化学结构改造得到的化合物4-羟基-3-甲氧基肉桂酸乙酯的生物活性及其除草机制,利用茎叶喷雾法和小杯法测定其对马唐和反枝苋的生物活性,基于生理生化指标及功能基因表达量对其除草作用机制进行研究。结果表明:4-羟基-3-甲氧基肉桂酸乙酯对马唐茎叶鲜重抑制中浓度IC50为46.27 mg/L;对反枝苋胚根和芽的IC50分别为129.94 mg/L和147.33 mg/L,且在500 mg/L浓度处理时可抑制反枝苋种子萌发;对拟南芥根长的IC50为43.82 mg/L,在160 mg/L浓度处理时拟南芥几乎停止生长、叶片发黄、根毛堆积。该化合物以1 000 mg/L浓度处理马唐叶片2、3、8 h后,电导率较对照组分别增加了22.70%、18.46%和25.62%;1 000 mg/L浓度处理下叶绿素a/b为2.43,较对照的3.62显著下降;处理后叶表微观结构观察发现化合物浓度越大,植物叶片表皮毛倒伏和褶皱越严重;拟南芥AT4G04820基因表达量显著下降,在处理45 min时下降最显著,与对照组相差42.52倍,微管蛋白含量下降,造成微管解离,从而抑制植物生长。表明4-羟基-3-甲氧基肉桂酸乙酯具有较强的除草活性,可能通过破坏细胞结构、抑制光合作用及阻止根生长等途径使杂草生长受到抑制甚至死亡。 相似文献
2.
玉米蛋白粉的芽前除草活性机制 总被引：1，自引：1，他引：0
通过比较玉米蛋白粉在无菌及带菌条件下的芽前除草活性和玉米蛋白粉培养液在除草活性试验前后游离氨含量的变化,探讨玉米蛋白粉的芽前除草活性机制。结果显示:在带菌条件下,玉米蛋白粉能有效抑制8种植物种子萌发时胚根的生长,当玉米蛋白粉中蛋白质含量为14mg/mL时,供试植物胚根的发育完全被抑制,但无菌条件下玉米蛋白粉的胚根生长抑制活性显著降低,对2种供试植物的胚根生长抑制率均低于34%;除草活性试验前各处理组玉米蛋白粉培养液中的游离氨含量小于0.01mg/L,除草活性试验后,在带菌条件下的玉米蛋白粉培养液游离氨含量显著上升,达到3.78～40.52mg/L,而在无菌条件下则保持不变。这表明玉米蛋白粉的芽前除草活性源于其产生的游离氨对种子萌发的抑制作用。 相似文献
3.
为了开发利用棉籽壳中的除草活性物质,分别以无水乙醇、正丁醇、石油醚和乙酸乙酯为溶剂,采用索氏提取法对棉籽壳中的活性物质进行了提取,并对各溶剂粗提物进行了除草活性测定。结果发现:用无水乙醇提取的粗提物对稗草生长的抑制活性最高,经气相色谱-质谱(GC-MS)联用分析,发现该粗提物中主要含有甘油、三环己基3-烯-6-辛酮、4-乙烯基-2-甲氧基苯酚、(邻甲基苯酚)-2-溴-2氯-乙酰酯、十四酸、十四酸乙酯、十六烷酸、辛酸异戊酯和亚油酸9种化合物。进一步的除草活性测定结果表明,亚油酸、辛酸异戊酯、4-乙烯基-2-甲氧基苯酚和(邻甲基苯酚)-2-溴-2氯-乙酰酯4种化合物对稗草表现出一定的除草活性,其中亚油酸活性最强,其IC50值为14.5 mg/L。 相似文献
4.
为了进一步明确牡丹叶及其不同溶剂提取物的化感活性大小,于室内采用琼脂混粉法测定了牡丹叶粉末在不同浓度下对生菜、小麦、黄瓜、稗、夏至草、播娘蒿和独行菜等7种受体植物幼苗生长的影响.结果表明,虽然在低浓度下牡丹叶粉末对各受体植物幼苗生长的影响差异较大,但在高浓度时均表现出了较高的抑制作用,且对胚根(或种子根)的抑制效果明显高于对胚轴或胚芽鞘的抑制.计算对各受体植物胚根或种子根、胚轴或胚芽鞘的有效中浓度(EC50),生菜为0.93～5.25 g/L、小麦为1.20 ～4.65 g/L)、黄瓜为3.58～＞10.0 g/L、稗为0.64～3.36 g/L、夏至草为1.09～5.27 g/L、播娘蒿为1.02 ～9.65 g/L、独行菜为0.79 ～6.84 g/L,以稗的敏感性最高,黄瓜最低.继而探索了牡丹叶乙醇、甲醇和蒸馏水3种溶剂提取物对生菜幼苗生长的抑制效果,发现乙醇提取物的活性最高,提取浓度以80％ (V/V)为宜. 相似文献
5.
黄花棘豆抑制植物病原菌的活性成分研究 总被引：1，自引：0，他引：1
为了测定黄花棘豆(Oxytropis ochrocephala Bunge)提取物对常见病原真菌的活性, 明确其中的有效成分, 以黄花棘豆为材料, 结合生物活性追踪法, 对黄花棘豆的抑菌活性物质进行分离, 并利用现代波谱学技术进行结构鉴定。结果表明, 黄花棘豆乙醇提取物对供试4种病原真菌均表现出较强的活性, 10 mg/mL对番茄灰霉病菌的抑菌率达到82.08 %; 粗提物萃取后的二氯甲烷相和乙酸乙酯相为其活性部分, 10 mg/mL对番茄灰霉病菌的抑菌率分别为84.30 %和83.13 %; 从合并后的二氯甲烷和乙酸乙酯相中分离、鉴定得到了6个化合物, 其中3-羟基-4, 9-二甲氧基紫檀烷、3-羟基-9-甲氧基紫檀烷和3-羟基-8, 9-二甲氧基紫檀烷对供试病原菌表现较好的抑制活性; 3-羟基-4, 9-二甲氧基紫檀烷对番茄灰霉病菌的EC50值为10.42 μg/mL, 3-羟基-8, 9-二甲氧基紫檀烷对黄瓜枯萎病菌的EC50值为27.09 μg/mL。黄花棘豆提取物对病原真菌具有较好的抑制活性, 紫檀烷类化合物为其主要的活性成分, 具备进一步开发和应用的潜力。 相似文献
6.
为了寻找具有较高除草活性的异香豆素类化合物,设计合成了16个新型异香豆素噁二唑类化合物4a～4p,其结构均经核磁共振氢谱、碳谱及高分辨质谱确证。初步除草活性测定结果表明,部分目标化合物在500 mg/L下对马唐Digitaria sanguinalis L.和反枝苋Amaranthusretroflexus L.具有一定的除草活性,其中化合物4j（4-[5-（4-氯-苯基）-[1,2,4]二唑-3-基]-3-己基-6,7-二甲氧基异香豆素）的活性最好,对马唐和反枝苋的致死率分别为64%和62%。 相似文献
7.
虫酰肼对水稻二化螟的拒食、致死作用及田间效果 总被引：14，自引：0，他引：14
室内生测结果表明 ,虫酰肼 (RH- 5992 )对水稻二化螟 Chilo suppressalis具有较高的拒食活性 ,2mg/L以上可使 4龄二化螟在 2d内停止取食 ,而 0.2mg/L即可显著抑制其生长发育 ,导致幼虫最终不能化蛹。虫酰肼对不同日龄二化螟均具有较高活性 ,对初孵蚁螟 ,40mg/L的杀虫效果高达 97.8% ,对于 1～ 7日龄幼虫 ,120mg/L的防治效果均在 90 %以上。虫酰肼对二化螟的致死历程较长 ,致死时间因浓度和二化螟龄期不同而变化 ,浓度增加对 l～ 4龄各龄期致死时间影响较小,而 6龄时 ,随浓度增加 ,致死时间明显缩短 ;在同一低浓度下 ,随着虫龄增加 ,致死时间明显延长 ,高浓度下 ,致死时间与龄期增加无明显相关性。虫酰肼无杀卵活性 ,对卵寄生蜂安全。田间试验表明 ,20%虫酰肼 (F) 1.5L/hm2 对二化螟、大螟 Sesamiainferens、三化螟 Scirpophaga incertulas枯心和稻纵卷叶螟 Cnaphalocrocis medinalis均有良好的控制效果。 相似文献
8.
9.
为了探讨麦田常见杂草对苯磺隆敏感性差异的分子机制,测定了苯磺隆对4种杂草活性及对杂草体内靶标酶(ALS)和代谢酶(GSTs)的影响差异。结果表明,泽漆对苯磺隆的敏感性最低,IC50为123.16gai/hm2;猪殃殃和荠菜次之,分别为8.47、1.07gai/hm2;播娘蒿最敏感,为0.29gai/hm2。离体条件下,苯磺隆对播娘蒿、泽漆ALS的IC50值分别为6.40、54.90mgai/L。活体条件下,苯磺隆处理后,播娘蒿体内ALS活力低于对照,第9天降为对照的31.20%,而敏感性低的泽漆处理后1～2天ALS活力虽略有下降,但第3天明显提高,第4天达到峰值,为对照的2.90倍,此后逐渐恢复至对照水平。4种杂草本身所含GSTs活性存在较大差异,泽漆GSTs活性最高。经苯磺隆处理后,泽漆与猪殃殃GSTs活性明显提高,第4天时达到峰值,相对活性分别为1.23和1.25,并持续在较高水平;而荠菜、播娘蒿GSTs活性虽分别在第3、5天达到峰值,但多数时间相对活性低于1。结果表明,麦田不同杂草体内ALS的敏感性差异和GSTs的代谢差异是对苯磺隆敏感性不同的两个重要原因。 相似文献
10.
为了寻找具有较高除草活性的农药先导化合物,将吡唑环与双酰肼结构进行拼接,设计合成了13个未见报道的含吡唑环的双酰肼类目标化合物6a~6m,其结构均通过核磁共振氢谱及高分辨质谱确认。培养皿法测定结果表明:在200 mg/L下,化合物N'-(2-(2,4-二氯苯氧基)乙酰基)-3-(二氟甲基)-1-甲基-1H-吡唑-4-甲酰肼(6i)对小麦Triticum aestivum、油菜Brassicacampestris、高粱Sorghum bicolor、萝卜Raphanus sativus和黄瓜Cucumis sativus根、茎的抑制率均达80%以上。盆栽试验表明:在有效成分150 g/hm2剂量下,采用苗后茎叶喷雾处理,化合物6i对反枝苋Amaranthus retroflexus和鳢肠Eclipta prostrata的抑制率均达80%;相同剂量下采用苗前土壤喷雾处理,6i对反枝苋A. retroflexus的抑制率也达80%。 相似文献
11.
TRAN DANG KHANH TRAN DANG XUAN ILL MIN CHUNG SHINKICHI TAWATA 《Weed Biology and Management》2008,8(4):267-275
Barnyardgrass is one of the most noxious paddy weeds in the world and causes great trouble to many crops. In a bioassay, the aqueous extract of paddy soil infested with barnyardgrass showed phytotoxic action against the growth of the tested crops and paddy weeds, of which rice was the most suppressed among the crops. In contrast, barnyardgrass was the least affected paddy weed. By the use of a separation resin, 18 compounds belonging to terpenes, derivatives of cinnamic acid and ferulic acid, long‐chain fatty acids, and steroids that were potentially involved in the phytotoxic activities in barnyardgrass‐infested soil were isolated and identified by gas chromatography–mass spectrometry analysis. Of these, the quantities of linalool, 4‐terpinenol, coumaran, methyl phenethyl ketone, and methyl ester cinnamic acid were 1.42, 0.37, 0.02, 3.12, and 4.59 μg g?1 of the wet soil, respectively. The herbicidal activity was varied among these qualified test compounds, in which methyl phenethyl ketone and methyl ester cinnamic acid were more herbicidal than coumaran, linalool, and 4‐terpinenol. A mixture of these compounds was also the least inhibitive against the growth of barnyardgrass, but exerted strong suppression against that of rice and monochoria. The present study demonstrates that barnyardgrass possesses strong phytotoxic properties and releases plant growth inhibitors into the soil to compete with rice and other paddy weeds in its vicinity by a chemical pathway. 相似文献
12.
Lignin biosynthesis is essential for plant growth. 4‐Coumarate CoA ligase (4‐CL, EC6.2.1.12) is involved in the monolignol synthesis and occupies a key role in regulating carbon flow into the phenylpropanoid metabolism pathway. Naringenin, one of the metabolites in this pathway, is known as a potent in vitro inhibitor of 4‐CL. The growth of rice (Oryza sativa L. cv. Koshihikari), maize (Zea mays L. cv. Yellow corn) and Echinochloa oryzicola Vasing seedlings at the 2nd leaf stage was inhibited after continuous root application with 0.1 mmol L?1 naringenin for 1 week, although naringenin did not kill these gramineous plants. The highest inhibition of fresh weight increase was observed in maize, followed by rice and E. oryzicola. The symptoms in these plants were root browning, delay of leaf/root development and shoot dwarfing. Naringenin treatment increased the contents of 4‐CL substrates, cinnamic acid, 4‐coumaric acid, caffeic acid and ferulic acid from 1.2 to 7.2 times and from 1.2 to 3.5 times in shoots and roots, respectively, except for ferulic acid in E. oryzicola roots. It also caused a slight decrease of the lignin content and alteration of lignin constitutions in rice plants. These results suggested that the monolignol pathways after 4‐CL towards lignin has the possibility to be the novel action sites of plant growth retardants, although further investigations are needed to clarify the mode of action. 相似文献
13.
Yukio Nezu Masahiro Miyazaki Kazuhiko Sugiyama Nobuhide Wada Ikuo Kajiwara Takeshige Miyazawa 《Pest management science》1996,47(2):115-124
A new series of the O-pyrimidinylsalicylates was synthesized and their herbicidal activity was examined. Some of these compounds showed very strong herbicidal activity under pre- and post-emergent treatment conditions against various kinds of grass and broadleaf weeds. Among these compounds, O-(4, 6-dimethoxypyrimidin-2-yl) salicylic acid and its methyl ester were found to exhibit the highest activity. The herbicidal symptoms observed after the treatments included early cessation of plant growth followed by chlorosis, necrosis and plant death. The symptoms were similar to those caused by sulfonylureas and imidazolinones, which inhibit branched-chain amino acid biosynthesis. 相似文献
14.
Michael A. Venis 《Pest management science》1982,13(3):309-317
An esterase, that has been partially purified from oat tissues, catalyses the hydrolysis of the wild oat herbicide benzoylprop-ethyl and of the related esters of N-benzoyl-N-(3-chloro-4-fluorophenyl)-DL -alanine, including flamprop-methyl and flampropisopropyl. The enzyme is virtually stereospecific for the L -isomers in the racemic mixtures. Hydrolysis of flamprop-methyl in oat tissues shows similar enantiomeric discrimination, but the ethyl and isopropyl ester analogues are converted in vivo to the free acid with very little overall stereoselectivity. Oat tissues must, therefore, contain another enzyme, labile to isolation, that acts on the D -isomers of the higher esters. This was confirmed by showing that it is possible to manipulate the stereoselectivity of the de-esterification of the ethyl ester in vivo by selective inhibition of either the L -isomer pathway with paraoxon (diethyl 4-nitrophenyl phosphate), or the D -isomer route with piperonyl butoxide. The relationship of these findings to the superior herbicidal performance of the L -isomers of these esters, relative to their racemates, is discussed. 相似文献
15.
氟氯吡啶酯与双氟磺草胺复配的田间除草效果及其对作物安全性评价 总被引：7，自引：2，他引：5
氟氯吡啶酯属于人工合成激素类除草剂全新类别,是芳香基吡啶甲酸类家族的第1位成员,为明确其作用特点、除草活性、与双氟磺草胺复配后的除草效果以及对小麦和后茬作物的安全性,连续2年分别于小麦越冬前和返青初期施药,在冬小麦田进行了田间试验。结果表明,7.5 g/L氟氯吡啶酯EC在7.5 g/hm2用量下,对猪殃殃、播娘蒿防效较好,2次施药末次调查对猪殃殃防效为96.5%和100%,对播娘蒿防效为94.1%和81.1%;对麦瓶草防效较差,末次调查为57.1%和27.9%,对麦家公无效。复配制剂20%氟氯吡啶酯·双氟磺草胺WG在15、20、30 g/hm2用量下,对猪殃殃、播娘蒿、麦瓶草防效均较好,株防效为90.5%~100%,对麦家公防效略差,越冬前施药株防效为78.8%~98.6%,返青初期施药株防效为20.9%~82.5%;末次调查时杂草总鲜重防效为90.1%~98.2%,2次施药结果差异不显著。小麦田喷施该复配制剂15~45 g/hm2剂量,对小麦安全,未见任何药害症状;且对后茬作物玉米、大豆、花生、棉花、谷子均安全。 相似文献
16.
Inhibition of S-cysteinyl-hydroxychlorpropham transferase from oat (Avena sativa L.) by various compounds was studied. The β-O-glucoside of the substrate, isopropyl-3′-chloro-4′-hydroxycarbanilate (4-hydroxychlorpropham), and isopropyl-3′-chlorocarbanilate (chlorpropham) did not inhibit the enzyme. Isopropyl-5′-chloro-2′-hydroxycarbanilate (2-hydroxy-5-chlorpropham), was a competitive inhibitor with respect to 4-hydroxychlorpropham, but 2-β-O-glucosyl-5-chlorpropham was not an inhibitor. The inhibition patterns exhibited by 2-hydroxy-5-chlorpropham and other aryl-hydroxylated analogs suggested that the site of aryl-cysteine thioether conjugation might be the ortho (2′) aromatic carbon. Inhibitions by 3-chloro-4-hydroxyaniline and ferulic acid suggest that related phenols and/or naturally occurring phenolic plant acids could serve as substrates for the enzyme system. Glutathione was a competitive inhibitor with respect to cysteine and could also form a conjugate with 4-hydroxychlorpropham. Atypical inhibitions of cysteine conjugation by cysteine ethyl ester or firefly d-luciferin were described. Similarities between S-cysteinyl-hydroxychlorpropham transferase and firefly luciferase were noted. 相似文献
17.
Ruling factors governing pre-emergence herbicidal activity were analysed for 16 photosynthesis-inhibiting 5-hydroxy-3-methyl-2–oxo-imidazolidine-1-carboxamide derivatives. Herbicidal performance was quantified by the reduction in area of experimental weed vegetation, measured by a computer-aided image analysis system. A system for fluorometric estimation of photosynthesis inhibitor concentration in aqueous solution greatly facilitated determination of the soil adsorption coefficients (Kd). Maximum herbicidal performance was found for N-sec-butyl-5-hydroxy-3-methyl-2-oxo-imidazolidine-1-carboxamide, a compound with the second lowest soil adsorptivity and average photosynthesis-inhibiting activity. A multiple regression analysis suggested that herbicidal performance of the soil-applied imidazolidine derivatives was determined by a balance between Kd and photosynthesis-inhibiting activity. In the present experimental system, however, the main influence was attributed to Kd. 相似文献