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1.
Pestic Biochem Physiol ; 203: 105984, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39084788

ABSTRACT

This study focuses on dilution effect of target-site resistance (TSR) to acetolactate synthase (ALS) inhibitors in Schoenoplectiella juncoides, which harbors two ALS genes, ALS1 and ALS2. We assessed gene expression, enzyme activity, and whole-plant resistance profiles across four S. juncoides lines: the susceptible line, the parental resistant lines with a homozygous mutation in either ALS1 or ALS2, and the bred progeny line with homozygous mutations in both ALS1 and ALS2. Gene expression and enzyme function showed a proportional relationship that the expression ratios of ALS1 to ALS2, approximately 70:30, were consistent with the functional ratio predicted by the double-sigmoidal plateau positions observed in enzyme assays. However, at the whole-plant level, resistance did not correlate to the putative abundance of susceptible enzyme, but the parental lines showed similar resistance to each other despite different enzyme-level resistances. This suggests a non-proportional mechanism in the reflection of physiological enzymatic profiles to whole-plant resistance profiles. These findings highlight the complexity of herbicide resistance and the need for further research to understand the mechanisms that influence resistance outcomes. Understanding these relationships is essential for developing strategies to manage herbicide resistance effectively.


Subject(s)
Acetolactate Synthase , Cyperaceae , Herbicide Resistance , Herbicides , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Acetolactate Synthase/antagonists & inhibitors , Herbicide Resistance/genetics , Herbicides/pharmacology , Cyperaceae/genetics , Cyperaceae/drug effects , Plant Proteins/genetics , Plant Proteins/metabolism , Gene Expression Regulation, Plant/drug effects , Mutation , Genes, Plant
2.
Pestic Biochem Physiol ; 203: 105985, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39084789

ABSTRACT

Avena fatua L. is one of the most damaging and malignant weeds in wheat fields in China. Fenoxaprop-P-ethyl, mesosulfuron-methyl, and isoproturon, which belong to Acetyl-CoA carboxylase- (ACCase), acetolactate synthase- (ALS), and photosystem II- (PS II) inhibitors, respectively, are commonly used in wheat fields and have a long history of use on A. fatua. An A. fatua population (R) resistant to fenoxaprop-P-ethyl, mesosulfuron-methyl, and isoproturon was collected from a wheat field in 2020. This study explored the mechanisms of target site resistance (TSR) and non-target site resistance (NTSR) in the multi-resistant A. fatua. Whole-plant bioassays showed that the R population had evolved high resistance to fenoxaprop-P-ethyl and moderate resistance to mesosulfuron-methyl and isoproturon. However, no mutations were detected in the ACCase, ALS, or psbA genes in the R population. In addition, the ACCase and ALS gene expression levels in the R group were significantly higher than those in the susceptible population (S) after treatment with fenoxaprop-P-ethyl or mesosulfuron-methyl. In vitro ACCase and ALS activity assays showed that ACCase and ALS from the R population were insensitive to fenoxaprop and mesosulfuron-methyl, respectively, with resistance indices 6.12-fold and 17.46-fold higher than those of the S population. Furthermore, pretreatment with P450 inhibitors significantly (P < 0.05) reversed the multi-resistant A. fatua's resistance to fenoxaprop-P-ethyl, mesosulfuron-methyl, and isoproturon. Sethoxydim, flucarbazone­sodium, chlortoluron, and cypyrafluone were effective in controlling multi-resistance A. fatua. Therefore, the overexpression of ACCase and ALS to synthesize sufficient herbicide-targeting proteins, along with P450-mediated metabolism, conferred resistance to fenoxaprop-P-ethyl, mesosulfuron-methyl, and isoproturon in the R population.


Subject(s)
Acetolactate Synthase , Acetyl-CoA Carboxylase , Herbicide Resistance , Herbicides , Oxazoles , Phenylurea Compounds , Propionates , Herbicide Resistance/genetics , Herbicides/pharmacology , Oxazoles/pharmacology , China , Phenylurea Compounds/pharmacology , Acetyl-CoA Carboxylase/genetics , Acetyl-CoA Carboxylase/metabolism , Propionates/pharmacology , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Poaceae/drug effects , Phenylpropionates/pharmacology , Plant Proteins/genetics , Plant Proteins/metabolism , Sulfonylurea Compounds
3.
Article in English | MEDLINE | ID: mdl-39013608

ABSTRACT

The industrial amino acid production workhorse, Corynebacterium glutamicum naturally produces low levels of 2,3,5,6-tetramethylpyrazine (TMP), a valuable flavor, fragrance, and commodity chemical. Here, we demonstrate TMP production (∼0.8 g L-1) in C. glutamicum type strain ATCC13032 via overexpression of acetolactate synthase and/or α-acetolactate decarboxylase from Lactococcus lactis in CGXII minimal medium supplemented with 40 g L-1 glucose. This engineered strain also demonstrated growth and TMP production when the minimal medium was supplemented with up to 40% (v v-1) hydrolysates derived from ionic liquid-pretreated sorghum biomass. A key objective was to take the fully engineered strain developed in this study and interrogate medium parameters that influence the production of TMP, a critical post-strain engineering optimization. Design of experiments in a high-throughput plate format identified glucose, urea, and their ratio as significant components affecting TMP production. These two components were further optimized using response surface methodology. In the optimized CGXII medium, the engineered strain could produce up to 3.56 g L-1 TMP (4-fold enhancement in titers and 2-fold enhancement in yield, mol mol-1) from 80 g L-1 glucose and 11.9 g L-1 urea in shake flask batch cultivation. ONE-SENTENCE SUMMARY: Corynebacterium glutamicum was metabolically engineered to produce 2,3,5,6-tetramethylpyrazine followed by a design of experiments approach to optimize medium components for high-titer production.


Subject(s)
Corynebacterium glutamicum , Culture Media , Glucose , Metabolic Engineering , Pyrazines , Corynebacterium glutamicum/genetics , Corynebacterium glutamicum/metabolism , Pyrazines/metabolism , Metabolic Engineering/methods , Culture Media/chemistry , Glucose/metabolism , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Lactococcus lactis/genetics , Lactococcus lactis/metabolism , Lactococcus lactis/enzymology , Carboxy-Lyases/genetics , Carboxy-Lyases/metabolism , Urea/metabolism
4.
J Agric Food Chem ; 72(29): 16140-16151, 2024 Jul 24.
Article in English | MEDLINE | ID: mdl-39007211

ABSTRACT

Given the prevalence of the malignant weed Chinese Sprangletop (Leptochloa chinensis (L.) Nees) in rice fields, the development of novel herbicides against this weed has aroused wide interest. Here, we report a novel diphenyl ether-pyrimidine hybrid, DEP-5, serving as a systematic pre/postemergence herbicide candidate for broad-spectrum weed control in rice fields, specifically for L. chinensis. Notably, DEP-5 exhibits over 80% herbicidal activity against the resistant biotypes even at 37.5 g a.i./ha under greenhouse conditions and has complete control of L. chinensis at 150 g a.i./ha in the rice fields. We uncover that DEP-5 acts as a noncompetitive inhibitor of acetohydroxyacid synthase (AHAS) with an inhibition constant (Ki) of 39.4 µM. We propose that DEP-5 binds to AHAS in two hydrophobic-driven binding modes that differ from commercial AHAS inhibitors. Overall, these findings demonstrate that DEP-5 has great potential to be developed into a herbicide for L. chinensis control and inspire fresh concepts for novel AHAS-inhibiting herbicide design.


Subject(s)
Acetolactate Synthase , Herbicides , Oryza , Plant Proteins , Plant Weeds , Poaceae , Weed Control , Herbicides/pharmacology , Herbicides/chemistry , Oryza/chemistry , Plant Weeds/drug effects , Plant Weeds/enzymology , Acetolactate Synthase/metabolism , Acetolactate Synthase/antagonists & inhibitors , Acetolactate Synthase/genetics , Plant Proteins/metabolism , Plant Proteins/genetics , Plant Proteins/antagonists & inhibitors , Poaceae/chemistry , Poaceae/enzymology , Poaceae/drug effects , Enzyme Inhibitors/pharmacology , Enzyme Inhibitors/chemistry , Pyrimidines/pharmacology , Kinetics , Phenyl Ethers/pharmacology , Phenyl Ethers/chemistry
5.
Pestic Biochem Physiol ; 202: 105912, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38879294

ABSTRACT

Herbicide resistance is a worldwide concern for weed control. Cucumis melo L. var. agrestis Naud. (C. melo) is an annual trailing vine weed that is commonly controlled by nicosulfuron, acetolactate synthase (ALS)-inhibiting herbicides. However, long-term use of this herbicide has led to the emergence of resistance and several nicosulfuron resistant populations of C. melo have been found. Here we identified a resistant (R) C. melo population exhibiting 7.31-fold resistance to nicosulfuron compared with a reference sensitive (S) population. ALS gene sequencing of the target site revealed no amino acid substitution in R plants, and no difference in enzyme activity, as shown by ALS activity assays in vitro. ALS gene expression was not significantly different before and after the application of nicosulfuron. Pretreatment with the cytochrome P450 monooxygenase (P450) inhibitor malathion reduced nicosulfuron resistance in the R population. RNA-Seq transcriptome analysis was used to identify candidate genes that may confer metabolic resistance to nicosulfuron. We selected genes with annotations related to detoxification functions. A total of 20 candidate genes (7 P450 genes, 1 glutathione S-transferase (GST) gene, 2 ATP-binding cassette (ABC) transporters, and 10 glycosyltransferase (GT)) were identified; 12 of them (7 P450s, 1 GST, 2 ABC transporters, and 2 GTs) were demonstrated significantly differential expression between R and S by quantitative real-time RT-PCR (qRT-PCR). Our findings revealed that the resistance mechanism in C. melo was nontarget-site based. Our results also provide a valuable resource for studying the molecular mechanisms of weed resistance.


Subject(s)
Acetolactate Synthase , Cucumis melo , Herbicide Resistance , Herbicides , Pyridines , Sulfonylurea Compounds , Herbicide Resistance/genetics , Sulfonylurea Compounds/pharmacology , Herbicides/pharmacology , Herbicides/toxicity , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Cucumis melo/genetics , Cucumis melo/drug effects , Pyridines/pharmacology , RNA-Seq , Gene Expression Profiling , Malathion/pharmacology , Gene Expression Regulation, Plant/drug effects , Plant Proteins/genetics , Plant Proteins/metabolism
6.
Pestic Biochem Physiol ; 202: 105946, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38879333

ABSTRACT

Eriochloa villosa (Thunb.) Kunth is a troublesome weed widely distributed in maize (Zea mays L.) fields in Northeast China. Many populations of E. villosa have evolved resistance to nicosulfuron herbicides, which inhibit acetolactate synthase (ALS). The objectives of this research were to confirm that E. villosa is resistant to nicosulfuron and to investigate the basis of nicosulfuron resistance. Whole-plant dose-response studies revealed that the R population had not developed a high level of cross-resistance and exhibited greater resistant (25.62-fold) to nicosulfuron than that of the S population and had not yet developed a high level of cross-resistance. An in vitro ALS activity assay demonstrated that the I50 of nicosulfuron was 6.87-fold greater in the R population than the S population. However, based on ALS gene sequencing, the target ALS gene in the R population did not contain mutations. Quantitative real-time polymerase chain reaction (qRT-PCR) revealed that ALS gene expression between the R and S populations was significantly different after nicosulfuron application, but no differences were observed in the gene copy number. After the cytochrome P450 inhibitor malathion or the GST inhibitor NBD-Cl was applied, the resistant E. villosa population exhibited increased sensitivity to nicosulfuron. Based on the activities of GSTs and P450s, the activities of the R population were greater than those of the S population after nicosulfuron application. This is the first report that the resistance of E. villosa to ALS inhibitors results from increased target gene expression and increased metabolism. These findings provide a theoretical foundation for the effective control of herbicide-resistant E. villosa.


Subject(s)
Acetolactate Synthase , Herbicide Resistance , Herbicides , Pyridines , Sulfonylurea Compounds , Sulfonylurea Compounds/pharmacology , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Acetolactate Synthase/antagonists & inhibitors , Herbicide Resistance/genetics , Herbicides/pharmacology , Pyridines/pharmacology , Plant Proteins/genetics , Plant Proteins/metabolism , Gene Expression Regulation, Plant/drug effects , Poaceae/genetics , Poaceae/drug effects
7.
Molecules ; 29(11)2024 May 21.
Article in English | MEDLINE | ID: mdl-38893290

ABSTRACT

Herbicides are useful tools for managing weeds and promoting food production and sustainable agriculture. In this study, we report on the development of a novel class of lipophilic pyrimidine-biphenyl (PMB) herbicides. Firstly, three PMBs, Ia, IIa, and IIIa, were rationally designed via a scaffold hopping strategy and were determined to inhibit acetohydroxyacid synthase (AHAS). Computational simulation was carried out to investigate the molecular basis for the efficiency of PMBs against AHAS. With a rational binding mode, and the highest in vitro as well as in vivo potency, Ia was identified as a preferable hit. Furthermore, these integrated analyses guided the design of eighteen new PMBs, which were synthesized via a one-step Suzuki-Miyaura cross-coupling reaction. These new PMBs, Iba-ic, were more effective in post-emergence control of grass weeds compared with Ia. Interestingly, six of the PMBs displayed 98-100% inhibition in the control of grass weeds at 750 g ai/ha. Remarkably, Ica exhibited ≥ 80% control against grass weeds at 187.5 g ai/ha. Overall, our comprehensive and systematic investigation revealed that a structurally distinct class of lipophilic PMB herbicides, which pair excellent herbicidal activities with new interactions with AHAS, represent a noteworthy development in the pursuit of sustainable weed control solutions.


Subject(s)
Herbicides , Pyrimidines , Herbicides/chemistry , Herbicides/pharmacology , Pyrimidines/chemistry , Pyrimidines/pharmacology , Acetolactate Synthase/antagonists & inhibitors , Acetolactate Synthase/metabolism , Acetolactate Synthase/chemistry , Biphenyl Compounds/chemistry , Biphenyl Compounds/antagonists & inhibitors , Molecular Docking Simulation , Plant Weeds/drug effects , Structure-Activity Relationship , Molecular Structure
8.
Biochem Biophys Res Commun ; 718: 150087, 2024 Jul 23.
Article in English | MEDLINE | ID: mdl-38735139

ABSTRACT

Flooding deprives plants of oxygen and thereby causes severe stress by interfering with energy production, leading to growth retardation. Enzymes and metabolites may help protect plants from waterlogging and hypoxic environmental conditions. Acetolactate synthase (ALS) is a key enzyme in the biosynthesis of branched-chain amino acids (BCAAs), providing the building blocks for proteins and various secondary metabolites. Additionally, under energy-poor conditions, free BCAAs can be used as an alternative energy source by mitochondria through a catabolic enzyme chain reaction. In this study, we characterized ALS-INTERACTING PROTEIN 1 (OsAIP1), which encodes the regulatory subunit of ALS in rice (Oryza sativa). This gene was expressed in all parts of the rice plant, and its expression level was significantly higher in submerged and low-oxygen environments. Rice transformants overexpressing OsAIP1 showed a higher survival rate under hypoxic stress than did non-transgenic control plants under the same conditions. The OsAIP1-overexpressing plants accumulated increased levels of BCAAs, demonstrating that OsAIP1 is an important factor in the hypoxia resistance mechanism. These results suggest that ALS proteins are part of a defense mechanism that improves the tolerance of plants to low-oxygen environments.


Subject(s)
Acetolactate Synthase , Gene Expression Regulation, Plant , Oryza , Plant Proteins , Oryza/genetics , Oryza/metabolism , Oryza/enzymology , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Plants, Genetically Modified , Stress, Physiological/genetics , Amino Acids, Branched-Chain/metabolism , Oxygen/metabolism , Protein Subunits/metabolism , Protein Subunits/genetics
9.
J Agric Food Chem ; 72(21): 12014-12028, 2024 May 29.
Article in English | MEDLINE | ID: mdl-38748759

ABSTRACT

Alopecurus aequalis Sobol. is a predominant grass weed in Chinese winter wheat fields, posing a substantial threat to crop production owing to its escalating herbicide resistance. This study documented the initial instance of an A. aequalis population (AHFT-3) manifesting resistance to multiple herbicides targeting four distinct sites: acetyl-CoA carboxylase (ACCase), acetolactate synthase, photosystem II, and 1-deoxy-d-xylulose-5-phosphate synthase. AHFT-3 carried an Asp-to-Gly mutation at codon 2078 of ACCase, with no mutations in the remaining three herbicide target genes, and exhibited no overexpression of any target gene. Compared with the susceptible population AHFY-3, AHFT-3 metabolized mesosulfuron-methyl, isoproturon, and bixlozone faster. The inhibition and comparison of herbicide-detoxifying enzyme activities indicated the participation of cytochrome P450s in the resistance to all four herbicides, with glutathione S-transferases specifically linked to mesosulfuron-methyl. Three CYP72As and a Tau class glutathione S-transferase, markedly upregulated in resistant plants, potentially played pivotal roles in the multiple-herbicide-resistance phenotype.


Subject(s)
Acetyl-CoA Carboxylase , Herbicide Resistance , Herbicides , Plant Proteins , Poaceae , Herbicide Resistance/genetics , Herbicides/pharmacology , Herbicides/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Acetyl-CoA Carboxylase/genetics , Acetyl-CoA Carboxylase/metabolism , Poaceae/genetics , Poaceae/metabolism , Poaceae/drug effects , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Cytochrome P-450 Enzyme System/genetics , Cytochrome P-450 Enzyme System/metabolism , Mutation , Plant Weeds/drug effects , Plant Weeds/genetics , Plant Weeds/metabolism
10.
Pest Manag Sci ; 80(9): 4757-4769, 2024 Sep.
Article in English | MEDLINE | ID: mdl-38809094

ABSTRACT

BACKGROUND: This study investigates factors contributing Amaranthus albus control failure in processing tomato fields in northern Israel. The study region is characterized by a significant climate gradient from east to west, providing the opportunity to investigate the effect of critical elements of the agricultural environment, e.g., temperature. Eight populations were collected from commercial fields in this region. Post-emergence herbicide efficacy of metribuzin, a photosystem II inhibitor, and rimsulfuron, an acetolactate synthase (ALS) inhibitor, was assessed through dose-response analyses at various growth stages. Temperature effects on control efficacy and resistance mechanisms were also explored. RESULTS: Standard metribuzin dose (X) was ineffective on A. albus plants with more than six true-leaves, whereas 2X dose proved effective. Rimsulfuron at 16X dose was ineffective on plants with more than four true-leaves. We report here the first case of target site resistance to ALS inhibitors in A. albus, due to point mutation in the ALS gene (Pro197 to Leu). Furthermore, our findings suggest potential involvement of CYT P450 enzymes in enhanced metabolizing of rimsulfuron. An overall decrease in dry weight was observed in response to both herbicides at 16/22 °C (P < 0.0001). Rimsulfuron was effective against only one population when applied at 28/34 °C. A possible fitness cost associated with target site-resistant biotypes was observed under low temperature conditions, leading to effective control. CONCLUSION: This regional-scale study highlights the challenges faced by growers, emphasizes the need for adapting management practices to the local climatic conditions and lays the groundwork for implementing location-specific weed management strategies in commercial fields. © 2024 The Author(s). Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.


Subject(s)
Acetolactate Synthase , Amaranthus , Herbicide Resistance , Herbicides , Temperature , Amaranthus/drug effects , Amaranthus/growth & development , Amaranthus/genetics , Herbicide Resistance/genetics , Herbicides/pharmacology , Acetolactate Synthase/metabolism , Acetolactate Synthase/genetics , Weed Control/methods , Israel , Triazines
11.
Sci Rep ; 14(1): 10544, 2024 05 08.
Article in English | MEDLINE | ID: mdl-38719860

ABSTRACT

The increasing amount of weeds surviving herbicide represents a very serious problem for crop management. The interaction between microbial community of soil and herbicide resistance, along with the potential evolutive consequences, are still poorly known and need to be investigated to better understand the impact on agricultural management. In our study, we analyzed the microbial composition of soils in 32 farms, located in the Northern Italy rice-growing area (Lombardy) with the aim to evaluate the relationship between the microbial composition and the incidence of resistance to acetolactate synthase (ALS) and acetyl-CoA carboxylase (ACCase) inhibiting herbicides in Echinochloa species. We observed that the coverage of weeds survived herbicide treatment was higher than 60% in paddy fields with a low microbial biodiversity and less than 5% in those with a high microbial biodiversity. Fungal communities showed a greater reduction in richness than Bacteria. In soils with a reduced microbial diversity, a significant increase of some bacterial and fungal orders (i.e. Lactobacillales, Malasseziales and Diaporthales) was observed. Interestingly, we identified two different microbial profiles linked to the two conditions: high incidence of herbicide resistance (H-HeR) and low incidence of herbicide resistance (L-HeR). Overall, the results we obtained allow us to make hypotheses on the greater or lesser probability of herbicide resistance occurrence based on the composition of the soil microbiome and especially on the degree of biodiversity of the microbial communities.


Subject(s)
Acetolactate Synthase , Acetyl-CoA Carboxylase , Echinochloa , Herbicide Resistance , Herbicides , Soil Microbiology , Italy/epidemiology , Herbicides/pharmacology , Acetolactate Synthase/antagonists & inhibitors , Acetolactate Synthase/genetics , Echinochloa/drug effects , Acetyl-CoA Carboxylase/genetics , Acetyl-CoA Carboxylase/antagonists & inhibitors , Plant Weeds/drug effects , Microbiota/drug effects , Biodiversity , Bacteria/drug effects , Bacteria/genetics , Bacteria/isolation & purification , Bacteria/classification , Soil/chemistry , Fungi/drug effects , Fungi/isolation & purification , Fungi/genetics
12.
Mol Biol Rep ; 51(1): 682, 2024 May 25.
Article in English | MEDLINE | ID: mdl-38796647

ABSTRACT

BACKGROUND: Control of blackleg disease of canola caused by the fungus Leptosphaeria maculans relies on strategies such as the inhibition of growth with fungicides. However, other chemicals are used during canola cultivation, including fertilizers and herbicides. There is widespread use of herbicides that target the acetolactate synthase (ALS) enzyme involved in branched chain amino acid synthesis and low levels of these amino acids within leaves of Brassica species. In L. maculans the ilv2 gene encodes ALS and thus ALS-inhibiting herbicides may inadvertently impact the fungus. METHODS AND RESULTS: Here, the impact of a commercial herbicide targeting ALS and mutation of the homologous ilv2 gene in L. maculans was explored. Exposure to herbicide had limited impact on growth in vitro but reduced lesion sizes in plant disease experiments. Furthermore, the mutation of the ilv2 gene via CRISPR-Cas9 gene editing rendered the fungus non-pathogenic. CONCLUSION: Herbicide applications can influence disease outcome, but likely to a minor extent.


Subject(s)
Acetolactate Synthase , Amino Acids, Branched-Chain , Herbicides , Leptosphaeria , Plant Diseases , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Plant Diseases/microbiology , Herbicides/pharmacology , Amino Acids, Branched-Chain/biosynthesis , Amino Acids, Branched-Chain/metabolism , Leptosphaeria/genetics , Leptosphaeria/pathogenicity , Mutation/genetics , Fungal Proteins/genetics , Fungal Proteins/metabolism , Gene Editing/methods , Plant Leaves/microbiology , CRISPR-Cas Systems/genetics , Brassica/microbiology , Ascomycota/pathogenicity , Ascomycota/genetics
13.
J Agric Food Chem ; 72(20): 11405-11414, 2024 May 22.
Article in English | MEDLINE | ID: mdl-38717990

ABSTRACT

This study investigated the multiple herbicide resistance (MHR) mechanism of one Echinochloa crus-galli population that was resistant to florpyrauxifen-benzyl (FPB), cyhalofop-butyl (CHB), and penoxsulam (PEX). This population carried an Ala-122-Asn mutation in the acetolactate synthase (ALS) gene but no mutation in acetyl-CoA carboxylase (ACCase) and transport inhibitor response1 (TIR1) genes. The metabolism rate of PEX was 2-fold higher, and the production of florpyrauxifen-acid and cyhalofop-acid was lower in the resistant population. Malathion and 4-chloro-7-nitrobenzoxadiazole (NBD-Cl) could reverse the resistance, suggesting that cytochrome P450 (CYP450) and glutathione S-transferase (GST) contribute to the enhanced metabolism. According to RNA-seq and qRT-PCR validation, two CYP450 genes (CYP71C42 and CYP71D55), one GST gene (GSTT2), two glycosyltransferase genes (rhamnosyltransferase 1 and IAAGLU), and two ABC transporter genes (ABCG1 and ABCG25) were induced by CHB, FPB, and PEX in the resistant population. This study revealed that the target mutant and enhanced metabolism were involved in the MHR mechanism in E. crus-galli.


Subject(s)
Cytochrome P-450 Enzyme System , Echinochloa , Herbicide Resistance , Herbicides , Mutation , Plant Proteins , Herbicide Resistance/genetics , Herbicides/pharmacology , Herbicides/metabolism , Echinochloa/genetics , Echinochloa/drug effects , Echinochloa/metabolism , Echinochloa/growth & development , Plant Proteins/genetics , Plant Proteins/metabolism , Cytochrome P-450 Enzyme System/genetics , Cytochrome P-450 Enzyme System/metabolism , Acetyl-CoA Carboxylase/genetics , Acetyl-CoA Carboxylase/metabolism , Plant Weeds/drug effects , Plant Weeds/genetics , Plant Weeds/metabolism , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Butanes , Nitriles , Sulfonamides , Uridine/analogs & derivatives
14.
Plant Sci ; 345: 112104, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38685454

ABSTRACT

Weeds are the primary biotic constraint affecting sesame growth and production. Here, we applied EMS mutagenesis to an elite sesame cultivar and discovered a novel point mutation in the sesame SiALS gene conferring resistance to imidazolinone, a group of acetolactate-synthase (ALS)-inhibitors. The mutant line exhibited high resistance to imazamox, an ALS-inhibitor, with hybrid plants displaying an intermediate response. Field-based validation confirmed the mutant line's substantial resistance, leading to a significantly higher yield under imazamox treatment. Under pre-emergence application of imazapic, the mutant plants sustained growth, whereas wild-type and weed were effectively controlled. Field trials using s-metolachlor and imazapic combined resulted in weed-free plots compared to untreated controls. Consequently, this treatment showed a significantly greater yield (2280 vs. 880 Kg ha-1) than the commercial practice (s-metolachlor). Overall, our study unveils the potential of utilizing this point mutation in sesame breeding programs, offering new opportunities for integrated weed management strategies for sesame cultivation. Developing herbicide-resistant crop plants holds promise for supporting sustainable production and addressing the challenges of weed infestations in sesame farming.


Subject(s)
Herbicide Resistance , Herbicides , Sesamum , Weed Control , Weed Control/methods , Herbicide Resistance/genetics , Sesamum/genetics , Sesamum/growth & development , Herbicides/pharmacology , Acetolactate Synthase/genetics , Plant Weeds/genetics , Plant Weeds/drug effects , Plant Proteins/genetics , Plant Proteins/metabolism , Mutation , Crops, Agricultural/genetics , Crops, Agricultural/growth & development
15.
Pestic Biochem Physiol ; 201: 105911, 2024 May.
Article in English | MEDLINE | ID: mdl-38685231

ABSTRACT

Ammannia auriculata Willd. is a noxious broadleaf weed, commonly infesting rice ecosystems across southern China. A putative resistant A. auriculata population (AHSC-5) was sampled from a rice field of Anhui Province, where bensulfuron-methyl (BM) was unable to control its occurrence. This study aimed to determine the sensitivities of the AHSC-5 population to common-use herbicides, and to investigate the underlying resistance mechanisms. The bioassays showed that the AHSC-5 population was 138.1-fold resistant to BM, compared with the susceptible population (JSGL-1). Pretreatment of malathion reduced the resistance index to 19.5. ALS sequencing revealed an Asp376Glu substitution in the AHSC-5 population, and in vitro ALS activity assays found that 50% activity inhibition (I50) of BM in AHSC-5 was 75.4 times higher than that of JSGL-1. Moreover, the AHSC-5 population displayed cross-resistance to pyrazosulfuron-ethyl (10.6-fold), bispyribac­sodium (3.6-fold), and imazethapyr (2.2-fold), and was in the process of evolving multiple resistance to synthetic auxin herbicides fluroxypyr (2.3-fold) and florpyrauxifen-benzyl (3.1-fold). This study proved the BM resistance in A. auriculata caused by the Asp376Glu mutation and P450-regulated metabolism. This multi-resistant population can still be controlled by penoxsulam, MCPA, bentazone, and carfentrazone-ethyl, which aids in developing targeted and effective weed management strategies.


Subject(s)
Acetolactate Synthase , Cytochrome P-450 Enzyme System , Herbicide Resistance , Herbicides , Acetolactate Synthase/genetics , Acetolactate Synthase/antagonists & inhibitors , Herbicides/pharmacology , Herbicide Resistance/genetics , Cytochrome P-450 Enzyme System/genetics , Cytochrome P-450 Enzyme System/metabolism , Malathion/pharmacology , Sulfonylurea Compounds/pharmacology , Plant Weeds/drug effects , Plant Weeds/genetics , Amino Acid Substitution
16.
Plant Physiol Biochem ; 210: 108597, 2024 May.
Article in English | MEDLINE | ID: mdl-38598868

ABSTRACT

BACKGROUND: Shortawn foxtail (Alopecurus aequalis Sobol.) is a noxious weed in China. The resistance of A. aequalis developed rapidly due to the long-term application of acetolactate synthase (ALS)-inhibiting herbicides. Here, a suspected mesosulfuron-methyl-resistant A. aequalis population, Aa-R, was collected from a wheat field in China. RESULTS: A dose‒response test showed that the Aa-R population has evolved a high level of resistance to mesosulfuron-methyl, and its growth was suppressed by imazamox, pyroxsulam and bispyribac-sodium. ALS gene sequence analysis revealed that a known resistance-related mutation (Pro-197-Thr) was present in the Aa-R population. Moreover, ALS gene overexpression was detected in the Aa-R population. The mesosulfuron-methyl resistance could be reversed by cytochrome P450 monooxygenase (CYP450) and glutathione S-transferase (GST) inhibitors. In addition, enhanced metabolism of mesosulfuron-methyl was detected in the Aa-R population compared with the susceptible population. NADPH-cytochrome P450 reductase and GST activities were strongly inducible in the Aa-R population. One CYP450 gene, CYP74A2, and one GST gene, GST4, were constitutively upregulated in the Aa-R population. Molecular docking results showed the binding affinity of CYP74A2 and GST4 for the tested ALS-inhibiting herbicides, respectively. CONCLUSION: This study confirmed that target-site resistance and non-target-site resistance involving CYP450 and GST were the main mechanisms involved in resistance in the mesosulfuron-methyl-resistant A. aequalis population.


Subject(s)
Acetolactate Synthase , Herbicide Resistance , Herbicides , Poaceae , Sulfonylurea Compounds , Herbicide Resistance/genetics , Sulfonylurea Compounds/pharmacology , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Herbicides/pharmacology , Poaceae/genetics , Poaceae/drug effects , Poaceae/metabolism , Cytochrome P-450 Enzyme System/genetics , Cytochrome P-450 Enzyme System/metabolism , Plant Proteins/genetics , Plant Proteins/metabolism , Glutathione Transferase/metabolism , Glutathione Transferase/genetics , Imidazoles/pharmacology , Gene Expression Regulation, Plant/drug effects , Mutation , Molecular Docking Simulation , Benzoates , Pyrimidines
17.
Pestic Biochem Physiol ; 201: 105882, 2024 May.
Article in English | MEDLINE | ID: mdl-38685248

ABSTRACT

White mustard, (Sinapis alba), a problematic broadleaf weed in many Mediterranean countries in arable fields has been detected as resistant to tribenuron-methyl in Tunisia. Greenhouse and laboratory studies were conducted to characterize Target-Site Resistance (TSR) and the Non-Target Site Resistance (NTSR) mechanisms in two suspected white mustard biotypes. Herbicide dose-response experiments confirmed that the two S. alba biotypes were resistant to four dissimilar acetolactate synthase (ALS)-pinhibiting herbicide chemistries indicating the presence of cross-resistance mechanisms. The highest resistance factor (>144) was attributed to tribenuron-methyl herbicide and both R populations survived up to 64-fold the recommended field dose (18.7 g ai ha-1). In this study, the metabolism experiments with malathion (a cytochrome P450 inhibitor) showed that malathion reduced resistance to tribenuron-methyl and imazamox in both populations, indicating that P450 may be involved in the resistance. Sequence analysis of the ALS gene detected target site mutations in the two R biotypes, with amino acid substitutions Trp574Leu, the first report for the species, and Pro197Ser. Molecular docking analysis showed that ALSPro197Ser enzyme cannot properly bind to tribenuron-methyl's aromatic ring due to a reduction in the number of hydrogen bonds, while imazamox can still bind. However, Trp574Leu can weaken the binding affinity between the mutated ALS enzyme and both herbicides with the loss of crucial interactions. This investigation provides substantial evidence for the risk of evolving multiple resistance in S. alba to auxin herbicides while deciphering the TSR and NTSR mechanisms conferring cross resistance to ALS inhibitors.


Subject(s)
Acetolactate Synthase , Herbicide Resistance , Herbicides , Malathion , Mutation , Sinapis , Acetolactate Synthase/genetics , Acetolactate Synthase/metabolism , Acetolactate Synthase/antagonists & inhibitors , Herbicides/pharmacology , Herbicide Resistance/genetics , Sinapis/drug effects , Sinapis/genetics , Malathion/pharmacology , Plant Proteins/genetics , Plant Proteins/metabolism , Arylsulfonates/pharmacology , Molecular Docking Simulation , Imidazoles/pharmacology
18.
Mol Ecol ; 33(11): e17368, 2024 Jun.
Article in English | MEDLINE | ID: mdl-38676602

ABSTRACT

Weedy rice, a pervasive and troublesome weed found across the globe, has often evolved through fertilization of rice cultivars with little importance of crop-weed gene flow. In Argentina, weedy rice has been reported as an important constraint since the early 1970s, and, in the last few years, strains with herbicide-resistance are suspected to evolve. Despite their importance, the origin and genetic composition of Argentinian weedy rice as well its adaptation to agricultural environments has not been explored so far. To study this, we conducted genotyping-by-sequencing on samples of Argentinian weedy and cultivated rice and compared them with published data from weedy, cultivated and wild rice accessions distributed worldwide. In addition, we conducted a phenotypic characterization for weedy-related traits, a herbicide resistance screening and genotyped accessions for known mutations in the acetolactate synthase (ALS) gene, which confers herbicide resistance. Our results revealed large phenotypic variability in Argentinian weedy rice. Most strains were resistant to ALS-inhibiting herbicides with a high frequency of the ALS mutation (A122T) present in Argentinian rice cultivars. Argentinian cultivars belonged to the three major genetic groups of rice: japonica, indica and aus while weeds were mostly aus or aus-indica admixed, resembling weedy rice strains from the Southern Cone region. Phylogenetic analysis supports a single origin for aus-like South American weeds, likely as seed contaminants from the United States, and then admixture with local indica cultivars. Our findings demonstrate that crop to weed introgression can facilitate rapid adaptation to agriculture environments.


Subject(s)
Acetolactate Synthase , Herbicide Resistance , Herbicides , Oryza , Oryza/genetics , Herbicide Resistance/genetics , Argentina , Acetolactate Synthase/genetics , Plant Weeds/genetics , Phenotype , Genotype , Adaptation, Physiological/genetics , Crops, Agricultural/genetics , Gene Flow , Agriculture , Mutation
19.
Pest Manag Sci ; 80(8): 3717-3725, 2024 Aug.
Article in English | MEDLINE | ID: mdl-38483107

ABSTRACT

BACKGROUND: Japanese brome (Bromus japonicus Thumb.) is one of the problematic annual weeds in winter wheat (Triticum aestivum L.) and is generally controlled by acetolactate synthase (ALS) inhibitors. Repeated use of the ALS inhibitor propoxycarbazone-Na resulted in the evolution of resistance to this herbicide in three B. japonicus populations, i.e., R1, R2, and R3 in Kansas (KS). However, the level of resistance and mechanism conferring resistance in these populations is unknown. The objectives of this research were to (i) evaluate the level of resistance to propoxycarbazone-Na in R1, R2, and R3 in comparison with a known susceptible population (S1), (ii) investigate the mechanism of resistance involved in conferring ALS-inhibitor resistance, and (iii) investigate the cross-resistance to other ALS inhibitors. RESULTS: Dose-response (0 to 16x; x = 44 g ai ha-1 of propoxycarbazone-Na) assay indicated 167, 125, and 667-fold resistance in R1, R2 and R3 populations, respectively, compared to S1 population. ALS gene sequencing confirmed the mutations resulting in amino acid substitutions, i.e., Pro-197-Thr (R3, R1)/Ser (R2, R1) bestowing resistance to these ALS inhibitors. Such amino acid substitutions also showed differential cross-resistance to sulfosulfuron, mesosulfuron-methyl, pyroxsulam, and imazamox among resistant populations. Pretreatment with malathion (a cytochrome P450 enzyme-inhibitor) followed by imazamox treatment suggested cross-resistance to this herbicide possibly via metabolism only in R3 population. CONCLUSION: Overall, these results confirm the first case of target-site based resistance to ALS inhibitors in B. japonicus in the US, highlighting the need for exploring herbicides with alternative modes of action to enhance weed control in winter wheat. © 2024 Society of Chemical Industry.


Subject(s)
Acetolactate Synthase , Bromus , Herbicide Resistance , Herbicides , Plant Proteins , Acetolactate Synthase/genetics , Acetolactate Synthase/antagonists & inhibitors , Acetolactate Synthase/metabolism , Bromus/enzymology , Bromus/drug effects , Bromus/genetics , Herbicide Resistance/genetics , Herbicides/pharmacology , Kansas , Plant Proteins/genetics , Plant Proteins/metabolism , Plant Proteins/antagonists & inhibitors , Plant Weeds/drug effects , Plant Weeds/genetics , Plant Weeds/enzymology
20.
Arch Biochem Biophys ; 754: 109962, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38499055

ABSTRACT

Acetohydroxyacid synthase (AHAS) is one of the key enzymes of the biosynthesis of branched-chain amino acids, it is also an effective target for the screening of herbicides and antibiotics. In this study we present a method for preparing Escherichia coli AHAS I holoenzyme (EcAHAS I) with exceptional stability, which provides a solid ground for us to re-investigate the in vitro catalytic properties of the protein. The results show EcAHAS I synthesized in this way exhibits similar function to Bacillus subtilis acetolactate synthase in its catalysis with pyruvate and 2-ketobutyrate (2-KB) as dual-substrate, producing four 2-hydroxy-3-ketoacids including (S)-2-acetolactate, (S)-2-aceto-2-hydroxybutyrate, (S)-2-propionyllactate, and (S)-2-propionyl-2-hydroxybutyrate. Quantification of the reaction indicates that the two substrates almost totally consume, and compound (S)-2-aceto-2- hydroxybutyrate forms in the highest yield among the four major products. Moreover, the protein also condenses two molecules of 2-KB to furnish (S)-2-propionyl-2-hydroxybutyrate. Further exploration manifests that EcAHAS I ligates pyruvate/2-KB and nitrosobenzene to generate two arylhydroxamic acids N-hydroxy-N-phenylacetamide and N-hydroxy-N-phenyl- propionamide. These findings enhance our comprehension of the catalytic characteristics of EcAHAS I. Furthermore, the application of this enzyme as a catalyst in construction of C-N bonds displays promising potential.


Subject(s)
Acetolactate Synthase , Escherichia coli , Acetolactate Synthase/chemistry , Glycogen Synthase , Hydroxybutyrates , Pyruvates , Holoenzymes
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