ABSTRACT
ABSTRACT: This study aimed to evaluate the antagonistic effect of the mixture ofacetyl coenzyme-A carboxylase (ACCase) enzyme inhibiting herbicides and auxin herbicides in Lolium multiflorum and to determine mechanisms to mitigate this possible effect. The first experiments were conducted by associating the herbicide clethodim (108 g a.i. ha−1), quizalofop-p-ethyl (54 g a.i. ha−1), and clethodim + quizalofop-p-ethyl (108+54 g a.i. ha−1) with 2,4-D (1005 g a.e. ha−1) or triclopyr (720 g a.e. ha−1), in addition to the sole application of the respective graminicides. Another experiment included clethodim (54; 81; 108; 162; 216 g a.i. ha−1), quizalofop-p-ethyl (27; 40.5; 54; 81; 108 g a.i. ha−1), and clethodim + quizalofop-p-ethyl (54+27; 81+40.5; 108+54; 162+81; 216+108 g a.i. ha−1) mixed with 2,4-D (1005 g a.e. ha−1), or triclopyr (720 g a.e. ha−1), in addition to the control treatments without herbicide application. In the second experiment, herbicides clethodim (108 g a.i. ha−1), quizalofop-p-ethyl (54 g a.i. ha−1), and clethodim + quizalofop-p-ethyl (108+54 g a.i. ha−1) in combination with the herbicides 2,4-D (1005 g a.e. ha−1) or triclopyr (720 g a.e. ha−1)had malathion (1000 g a.i. ha−1) or glyphosate (720 g a.e. ha−1) mixed, in addition to the sole applications of the graminicides. The herbicide clethodim + quizalofop-p-ethyl did not present an antagonistic interaction with the auxin herbicides, and obtained 85% weed control. To obtain control similar to the sole application of this graminicide, the dose of the herbicide clethodim needs to be increased by 20%. However, the mixture of the herbicide quizalofop-p-ethyl with 2,4-D and triclopyr affects the ryegrass control. The use of strategies that increase the absorption of ACCase herbicides or the inhibition of P450 enzymes are ways to mitigate the antagonistic effect caused by the association of the two auxin herbicides.
RESUMO: O objetivo do trabalho foi avaliar o efeito antagônico da mistura de herbicidas inibidores da enzima ACCase e herbicidas auxínicos em Lolium multiflorum e determinar mecanismos de mitigação deste possível efeito. No primeiro momento foram conduzidos experimentos associando o herbicida clethodim (108 g i.a. ha-1), quizalofop-p-ethyl (54 g i.a. ha-1) e clethodim + quizalofop-p-ethyl (108 + 54 g i.a. ha-1) com 2,4-D (1005 g e.a. ha-1) ou triclopyr (720 g e.a. ha-1), além da aplicação isolada dos respectivos graminicidas. Outro experimento contou com clethodim (54; 81; 108; 162; 216 g i.a ha-1), quizalofop-p-ethyl (27; 40,50; 54; 81; 108 g i.a ha-1) e clethodim + quizalofop-p-ethyl (54 + 27; 81 + 40,50; 108 +54; 162 +81; 216 + 108 g i.a ha-1) em mistura com 2,4-D (1005 g e.a ha-1) ou triclopyr (720 g e.a. ha-1), além das testemunhas sem aplicação herbicida. No segundo momento os herbicidas clethodim (108 g i.a. ha-1), quizalofop-p-ethyl (54 g i.a. ha-1) e clethodim + quizalofop-p-ethyl (108 + 54 g i.a. ha-1) em associação com os herbicidas 2,4-D (1005 g e.a ha-1) ou triclopyr (720 g e.a. ha-1), contaram com adição de malathion (1000 g i.a. ha-1) ou glyphosate (720 g e.a. ha-1), além das aplicações isoladas dos graminicidas. O herbicida clethodim + quizalofop-p-ethyl não apresentou interação antagônica com os herbicidas auxínicos, obtendo controle de 85%. Já para o herbicida clethodim é necessário o aumento de dose em 20 % é capaz de obter controle similar a aplicação isolada deste graminicida. Porém para o herbicida quizalofop-p-ethyl a mistura com os herbicidas 2,4-D e triclopyr repercute na diminuição do controle do azevém. O uso de estratégias que aumente a absorção do herbicida inibidor de ACCase ou a inibição das enzimas P450 são formas de mitigar o efeito antagônico causado pela associação destes dois tipos de herbicidas.
ABSTRACT
BACKGROUND: Quizalofop-p-ethyl (QPE), a unitary R configuration aromatic oxyphenoxypropionic acid ester (AOPP) herbicide, was widely used and had led to detrimental environmental effects. For finding the QPEdegrading bacteria and promoting the biodegradation of QPE, a series of studies were carried out. RESULTS: A QPE-degrading bacterial strain YC-XJ1 was isolated from desert soil and identified as Methylobacterium populi, which could degrade QPE with methanol by cometabolism. Ninety-seven percent of QPE (50 mg/L) could be degraded within 72 h under optimum biodegradation condition of 35°C and pH 8.0. The maximum degradation rate of QPE was 1.4 mg/L/h, and the strain YC-XJ1 exhibited some certain salinity tolerance. Two novel metabolites, 2-hydroxy-6-chloroquinoxaline and quinoxaline, were found by high-performance liquid chromatography/mass spectroscopy analysis. The metabolic pathway of QPE was predicted. The catalytic efficiency of strain YC-XJ1 toward different AOPPs herbicides in descending order was as follows: haloxyfop-pmethyl ≈ diclofop-methyl ≈ fluazifop-p-butyl N clodinafop-propargyl N cyhalofop-butyl N quizalofop-p-ethyl N fenoxaprop-p-ethyl N propaquizafop N quizalofop-p-tefuryl. The genome of strain YC-XJ1 was sequenced using a combination of PacBio RS II and Illumina platforms. According to the annotation result, one α/ß hydrolase gene was selected and named qpeh1, for which QPE-degrading function has obtained validation. Based on the phylogenetic analysis and multiple sequence alignment with other QPE-degrading esterases reported previously, the QPEH1 was clustered with esterase family V. CONCLUSION: M. populi YC-XJ1 could degrade QPE with a novel pathway, and the qpeh1 gene was identified as one of QPE-degrading esterase gene.