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Florpyrauxifen-benzyl is an herbicide that has been developed in recent years. Its degradation mode in paddy soil environments is not clear. In this study, the degradation dynamics in paddy soil and water were studied by ultrahigh-performance liquid chromatography. Microbial degradation was the main degradation pathway. Using third-generation high-throughput sequencing technology, the changes in the soil bacterial community structure were studied. After 30 days of application, compared with the control group (F0), the abundance of Sphingomonas, Lysobacter, and Flavisolibacter in the recommended and repeated application groups (F1, F5 and F10) increased significantly, and uncultured bacterium and Terrimonas decreased significantly. Compared with the F0 and F1 groups, the species diversity of the F0 and F1 groups showed a significant increase over time. The species diversity of the F5 and F10 groups decreased significantly on Days 5 and 15. On Day 30, the recovery even exceeded that of the control group. Luteimonas and five other genera were positively correlated with herbicide residues, and Pseudolabrys and two other genera were negatively correlated. Repeated application showed a significant effect on the structure of the soil bacterial community, mainly showing a trend of a significant decrease in the initial stage and gradual recovery in the later stage. The results will guide the safe and rational use of florpyrauxifen-benzyl and provide a scientific basis for florpyrauxifen-benzyl dynamic supervision of environmental pollution and protection of black soil in Northeast China.

In order to improve crop yield per unit area, pinoxaden was widely used in weed control in the field to better degrade the residual pinoxaden in the soil. In this experiment, 14 strains were domesticated and isolated from soil samples using pinoxaden as the only carbon and nitrogen source, and the highly degraded strain was T4P20-1. The effects of different pH values, inoculation amount and culture time on the growth and degradation rate of strain T4P20-1 were studied. The optimal growth conditions of strain T4P20-1 were determined, and the degradation rate reached 92.23%. The morphological characteristics of strain T4P20-1 were determined by optical microscope. The strain T4P20-1 was identified as Acinetobacter Pittii by physiological and biochemical characteristics and 16S rDNA homology analysis, and the nucleic acid sequence was submitted to Gentbank to obtain the accession number MW350066. Through gene sequencing, the whole genome framework of strain T4P20-1 and database annotations of GO, KEGG, COG, CAZymes and PHI were obtained. Meanwhile, genes related to herbicide degradation were predicted by gene functional annotations. There was a negative correlation between herbicide and seed germination rate, bud length and root length of maize susceptible to subsequent crop. In conclusion, the strains screened in this study have certain remediation effects on soil contaminated by pinoxaden. It provides a new choice for the degradation of pinoxaden in the future. It can increase crop yields and reduce food security risks.

The evolution of insect resistance to pesticides poses a continuing threat to agriculture and human health. While much is known about the proximate molecular and biochemical mechanisms that confer resistance, far less is known about the regulation of the specific genes/gene families involved, particularly by trans-acting factors such as signal-regulated transcription factors. Here we resolve in fine detail the trans-regulation of CYP6CM1, a cytochrome P450 that confers resistance to neonicotinoid insecticides in the whitefly Bemisia tabaci, by the mitogen-activated protein kinase (MAPK)-directed activation of the transcription factor cAMP-response element binding protein (CREB). Reporter gene assays were used to identify the putative promoter of CYP6CM1, but no consistent polymorphisms were observed in the promoter of a resistant strain of B. tabaci (imidacloprid-resistant, IMR), which overexpresses this gene, compared to a susceptible strain (imidacloprid-susceptible, IMS). Investigation of potential trans-acting factors using in vitro and in vivo assays demonstrated that the bZIP transcription factor CREB directly regulates CYP6CM1 expression by binding to a cAMP-response element (CRE)-like site in the promoter of this gene. CREB is overexpressed in the IMR strain, and inhibitor, luciferase, and RNA interference assays revealed that a signaling pathway of MAPKs mediates the activation of CREB, and thus the increased expression of CYP6CM1, by phosphorylation-mediated signal transduction. Collectively, these results provide mechanistic insights into the regulation of xenobiotic responses in insects and implicate both the MAPK-signaling pathway and a transcription factor in the development of pesticide resistance.

Anaerobic digestion technology mitigates agricultural organic waste pollution, thereby alleviating the energy crisis. Biochar materials increase the utilisation rate of biomass resources and promote the enrichment and growth of microorganisms. Biochar is an effective exogenous additive that stabilises the anaerobic digestion, improves anaerobic digestion efficiency and gas production. Herein, biochar materials were prepared from rice straw utilising the sequencing batch anaerobic digestion process. The biochar microstructure was characterised by scanning electron microscopy (SEM) and Brunauer–Emmett–Teller (BET) analysis, and microbial succession and metabolic pathways were analysed using 16S rRNA sequencing to reveal the molecular mechanisms. Rice straw biochar addition increased gas production during anaerobic fermentation. SEM revealed that numerous cocci and microbacteria became agglomerated and attached to the surface and pores of biochar, which was revealed by BET analysis to be a good habitat for microorganisms. After anaerobic digestion, the specific surface area and total pore volume of biochar decreased. 16S rRNA gene sequencing showed that biochar affected the abundance of certain bacteria and archaea. Biochar had no obvious effect on the function of bacterial flora but inhibited carbohydrate metabolism by bacteria and glycan biosynthesis and metabolism by archaea in the anaerobic fermentation system while promoting lipid metabolism by archaea. Biochar addition inhibited acetic acid production in the anaerobic fermentation system and promoted methane production based on hydrogen and carbon dioxide levels.

Atrazine is a long residual herbicide commonly used in maize fields. Although atrazine can effectively control weeds and improve crop yield, long-term application leads to continuous pollution in the agricultural ecological environment, especially in the soil ecosystem, and its impact on soil microorganisms is still not clear. Four methods were used in the experiment to clarify the effect of atrazine on the bacterial populations of cultivated soil layers of chernozem in a cold region in different periods: high-performance liquid chromatography (HPLC), colorimetry, microplate, and high-throughput sequencing. The level of residual atrazine in cold chernozem decreased from 4.645 to 0.077 mg/kg soil over time, and the residue gradually leached into deep soil and then decreased after accumulating to a maximum value. Atrazine significantly affected the activities of urease and polyphenol oxidase activity in the soil layers at different periods but had no significant effect on sucrase and phosphatase activity. Atrazine significantly reduced the diversity of microbial carbon source utilization and total activity in soil layers of 0–10 and 20–30 cm but only reduced the diversity of microbial carbon source utilization in the 10–20 cm layer. Atrazine had no significant effect on bacterial populations (10–12 phyla, 29–34 genera), but had a slight effect on the relative abundance of various groups. Atrazine significantly reduced the diversity of bacterial populations in cultivated soil layers of chernozem in a cold region, and the diversity of bacterial populations decreased with decreased residue. This lays a foundation for guiding the safe use of herbicides on farmland in Northeast China.

The evolution of insect resistance to pesticides poses a continuing threat to agriculture and human health. While much is known about the proximate molecular and biochemical mechanisms that confer resistance, far less is known about the regulation of the specific genes/gene families involved, particularly by trans-acting factors such as signal-regulated transcription factors. Here we resolve in fine detail the trans-regulation of CYP6CM1, a cytochrome P450 that confers resistance to neonicotinoid insecticides in the whitefly Bemisia tabaci, by the mitogen-activated protein kinase (MAPK)-directed activation of the transcription factor cAMP-response element binding protein (CREB). Reporter gene assays were used to identify the putative promoter of CYP6CM1, but no consistent polymorphisms were observed in the promoter of a resistant strain of B. tabaci (imidacloprid-resistant, IMR), which overexpresses this gene, compared to a susceptible strain (imidacloprid-susceptible, IMS). Investigation of potential trans-acting factors using in vitro and in vivo assays demonstrated that the bZIP transcription factor CREB directly regulates CYP6CM1 expression by binding to a cAMP-response element (CRE)-like site in the promoter of this gene. CREB is overexpressed in the IMR strain, and inhibitor, luciferase, and RNA interference assays revealed that a signaling pathway of MAPKs mediates the activation of CREB, and thus the increased expression of CYP6CM1, by phosphorylation-mediated signal transduction. Collectively, these results provide mechanistic insights into the regulation of xenobiotic responses in insects and implicate both the MAPK-signaling pathway and a transcription factor in the development of pesticide resistance.

In order to solve the problem of soil, water pollution and sensitive crop drug damage caused by chlorosulfuron residue, and to provide degradation strain resources for microbial remediation of contaminated soil, a chlorimuron-ethyl-degrading strain T9DB-01 was isolated from chlorosulfuron contaminated soil by the method of enrichment culture and step by step domestication. Strain T9DB-01 was identified as Pseudomonas sp. by morphological characteristics, physiological and biochemical analysis and 16S rDNA gene sequence analysis. The effects of temperature, pH value, substrate concentration, medium volume, and inoculation volume on the degradation of chlorsulfuron-methyl by strain T9DB-01 were investigated by single factor experiment. The degradation conditions of chlorosulfuron by strain T9DB-01 were optimized by orthogonal test and verification. Results show that 30 °C, pH 8.0, inoculum 4%, liquid volume 100 mL/250 mL, substrate concentration of 200 mg/L, cultured for 5 d, the strain degraded 93.7% chlorsulfuron-methyl. The degrading strain has certain application potential for bioremediation of chlorsulfuron-contaminated soil.为解决氯嘧磺隆残留对土壤、水体污染及后茬敏感作物药害问题，为污染土壤微生物修复提供降解菌种资源，文中采用富集培养、逐级驯化等方法，从氯嘧磺隆污染土壤中分离到1 株高效氯嘧磺隆降解菌T9DB-01，经形态特征、生理生化及16S rDNA 序列分析，鉴定为假单胞菌Pseudomonas sp.。采用单因素实验探究温度、pH值、底物浓度、装液量和接种量对菌株T9DB-01 降解氯嘧磺隆的影响，采用正交试验及验证，优化菌株T9DB-01对氯嘧磺隆降解条件。结果表明，在30 ℃，pH 8.0，底物浓度200 mg/L，装液量100 mL/250 mL，接种量4%的条件下，5 d 后降解率达到93.7%。该降解菌株对氯嘧磺隆污染土壤原位生物修复具有一定的应用潜力。.

The main purpose of this study was to explore the effects of the recommended usage level and twice the recommended usage level of the long-acting herbicide fomesafen on the soil enzymes and microbial community structure in chernozems of soybean fields. Culturable microbial biomass and phospholipid fatty acids (PLFA) were used as the main references for this evaluation. The digestion curve of fomesafen in soil conforms to the law of a single exponential function. The activities of four soil enzymes decreased significantly when exposed to twice the recommended amount, and then returned to the control level. The inhibition of the fungal and bacterial biomass section of culturable microorganisms in soil at twice the recommended usage level was greater than that under the recommended usage level, and this dosage also stimulated the rapid recovery of the initial level of fungal biomass before the application of fomesafen. The PLFA analysis showed that the ratio of GN/GP decreased significantly, and soil pressure increased significantly. Compared with the recommended usage level, the effect of twice the recommended usage level of fomesafen on soil microbial community structures was more significant. This provides a reference for environmental location recommendations, environmental safety assessments, and the rational use of herbicides.

Plants protect themselves with a vast array of toxic secondary metabolites, yet most plants serve as food for insects. The evolutionary processes that allow herbivorous insects to resist plant defenses remain largely unknown. The whitefly Bemisia tabaci is a cosmopolitan, highly polyphagous agricultural pest that vectors several serious plant pathogenic viruses and is an excellent model to probe the molecular mechanisms involved in overcoming plant defenses. Here, we show that, through an exceptional horizontal gene transfer event, the whitefly has acquired the plant-derived phenolic glucoside malonyltransferase gene BtPMaT1. This gene enables whiteflies to neutralize phenolic glucosides. This was confirmed by genetically transforming tomato plants to produce small interfering RNAs that silence BtPMaT1, thus impairing the whiteflies' detoxification ability. These findings reveal an evolutionary scenario whereby herbivores harness the genetic toolkit of their host plants to develop resistance to plant defenses and how this can be exploited for crop protection.

The whitefly (Bemisia tabaci) is a cosmopolitan and devastating pest of agricultural crops and ornamentals. B. tabaci causes extensive damage by feeding on phloem and by transmitting plant viruses. Like many other organisms, insects depend on amino acid transporters (AATs) to transport amino acids into and out of its cells. We present a genome-wide and transcriptome-wide investigation of the following two families of AATs in B. tabaci biotype B: amino acid/auxin permease (AAAP) and amino acid/polyamine/organocation (APC). A total of 14 putative APCs and 25 putative AAAPs were identified, and a 10-paralog B. tabaci-specific expansion of AAAPs was found by maximum likelihood phylogeny. Detailed gene structure information revealed that 9 members of the B. tabaci-specific AAAP family expansion closely situated on a same scaffold. Expression profiling of the B. tabaci B APC and AAAP genes as affected by stage and plant host showed diverse expression patterns. The analysis of evolutionary rates indicated that purifying selection can explain the B. tabaci-specific AAAP expansion. RNA interference (RNAi)-mediated suppression of two AAAP genes (BtAAAP15 and BtAAAP21) significantly increased the mortality of B. tabaci B adults. The results provide a foundation for future functional analysis of APC and AAAP genes in B. tabaci.

The whitefly (Bemisia tabaci), an important invasive pest that causes severe damage to crops worldwide, has developed resistance to a variety of insecticides. Carboxylesterases (COEs) are important multifunctional enzymes involved in the growth, development, and xenobiotic metabolism of insects. However, systematic studies on the COEs of B. tabaci are scarce. Here, 42 putative COEs in different functional categories were identified in the Mediterranean species of B. tabaci (B. tabaci MED) based on a genome database and neighbor-joining phylogeny. The expression patterns of the COEs were affected by the development of B. tabaci. The expression levels of six COEs were positively correlated with the concentration of imidacloprid to which B. tabaci adults were exposed. The mortality of B. tabaci MED adults fed dsBTbe5 (67.5%) and dsBTjhe2 (58.4%) was significantly higher than the adults fed dsEGFP (41.1%) when treated with imidacloprid. Our results provide a basis for functional research on COEs in B. tabaci and provide new insight into the imidacloprid resistance of B. tabaci.

Understanding the influence of fertilizer on soil quality is vital to agricultural management, yet there are few studies, particularly in black soil. In this study, soils under various treatments, namely no fertilizer, bio-organic + humic acid, bio-organic + chemical, and chemical fertilizer, were sampled to identify their major physiochemical properties, and to investigate the fungal community structure using environmental sequencing techniques. Physiochemical properties and fungal community structure were examined at four important stages of the maize life cycle: seedling, jointing, heading period, and maturity. We found that chemical fertilizer in the mature stage increased the soil available phosphorous (AP) content. Organic matter content was greatly affected by bio-organic + chemical fertilizer during the mature stage. Bio-organic + humic acid significantly increased soil phosphatase activity in maturing maize, whilst chemical fertilizers reduced invertase activity. Taken together, our results clearly illustrated that bio-organic + humic and chemical fertilization indirectly alter fungal community structure via changing soil properties (especially AP). Chemical fertilizer markedly heightened the AP content, thereby decreasing specific fungal taxa, particularly Guehomyces. OM was of positive connection with bio-organic + humic acid and Mortierella abundance, respectively, through RDA analysis, which are in agreement with our result that bio-organic + humic acid fertilization to some extent increased Mortierella abundance. Additionally, bio-organic + humic acid decreased the abundance of Fusarium and Humicola, suggesting that bio-organic + humic acid possibly could help control crop disease. These results help to inform our fundamental understanding of the interactions between fertilizers, soil properties, and fungal communities.

The whitefly, Bemisia tabaci, has developed a high level of resistance to thiamethoxam, a second generation neonicotinoid insecticide that has been widely used to control this pest. In this study, we assessed the level of cross-resistance, the activities of detoxifying enzymes, and the expression profiles of 23 glutathione S-transferase (GST) genes in a thiamethoxam-resistant ant and -susceptible strain of Bemisia tabaci Q. The thiamethoxam-resistant strain showed a moderate level of cross-resistance to another nicotinoid insecticide imidacloprid, a low level of cross-resistance to acetamiprid and nitenpyram, and no significant cross-resistance to abamectin and bifenthrin. Among detoxifying enzymes, only GSTs had significantly higher activity in the resistant strain than in the susceptible strain. Seven of 23 GST genes were over-expressed in the resistant strain relative to the susceptible strain. Using the technology of RNA interference to knockdown a GST gene (GST14), the results showed that silencing GST14 increased the mortality of whiteflies to thiamethoxam in Bemisia tabaci.

The diamondback moth, Plutella xylostella (L.), is a worldwide pest of cruciferous crops and can rapidly develop resistance to many chemical insecticides. Although insecticidal crystal proteins (i.e., Cry and Cyt toxins) derived from Bacillus thuringiensis (Bt) have been useful alternatives to chemical insecticides for the control of P. xylostella, resistance to Bt in field populations of P. xylostella has already been reported. A better understanding of the resistance mechanisms to Bt should be valuable in delaying resistance development. In this study, the mechanisms underlying P. xylostella resistance to Bt Cry1Ac toxin were investigated using two-dimensional differential in-gel electrophoresis (2D-DIGE) and ligand blotting for the first time. Comparative analyses of the constitutive expression of midgut proteins in Cry1Ac-susceptible and -resistant P. xylostella larvae revealed 31 differentially expressed proteins, 21 of which were identified by mass spectrometry. Of these identified proteins, the following fell into diverse eukaryotic orthologous group (KOG) subcategories may be involved in Cry1Ac resistance in P. xylostella: ATP-binding cassette (ABC) transporter subfamily G member 4 (ABCG4), trypsin, heat shock protein 70 (HSP70), vacuolar H(+)-ATPase, actin, glycosylphosphatidylinositol anchor attachment 1 protein (GAA1) and solute carrier family 30 member 1 (SLC30A1). Additionally, ligand blotting identified the following midgut proteins as Cry1Ac-binding proteins in Cry1Ac-susceptible P. xylostella larvae: ABC transporter subfamily C member 1 (ABCC1), solute carrier family 36 member 1 (SLC36A1), NADH dehydrogenase iron-sulfur protein 3 (NDUFS3), prohibitin and Rap1 GTPase-activating protein 1. Collectively, these proteomic results increase our understanding of the molecular resistance mechanisms to Bt Cry1Ac toxin in P. xylostella and also demonstrate that resistance to Bt Cry1Ac toxin is complex and multifaceted.

Fomesafen is widely used to control broad-leaved weeds in oil-bearing crops such as soybean and peanut. However, fomesafen has a long residual period in soil. If it is not used properly, it will cause damage to sensitive crops in different degrees. In this paper, the effects of fomesafen-degrading strains on the residue of fomesafen and the structure of soil microbial community were studied. Under field experiments, a microbial solution containing fomesafen-degrading Shigella flexneri FB5 was sprayed. We then detected residual fomesafen in the soil using high-performance liquid chromatography and phospholipid fatty acid content using gas chromatography-mass spectrometry. Analysis of variance suggested that the addition of fomesafen-degrading strains had a significant effect on soil microorganisms, as revealed by changes in the fungi/bacteria index, gram-negative/gram-positive bacteria ratio, stress indicators, and total phospholipid fatty acids. To sum up, our results show that the use of fomesafen-degrading strains can reduce the toxicity of fomesafen.

Glutathione-S-transferases (GST) comprise a multifunctional protein superfamily, which plays important roles as detoxifiers and antioxidants in insects. The GST in Asian corn borer has not been previously characterized. In this study, we cloned, characterized, and expressed the complete GST genes from the midgut of Asian corn borer. Furthermore, we designed htL4440-OfGST vector to exploit this gene for RNA interference (RNAi) strategy to control this pest. A complete GST cDNA sequence in Asian corn borer was obtained by reverse transcription polymerase chain reaction (RT-PCR) and rapid amplification of cDNA ends technology. The gene was 887bp in length and contained a 705bp open reading frame and 5′ UTR and 3′ UTR lengths of 89 and 93bp, respectively. The putative sequence encoded a putative 234 amino acid residue peptide and had a predicted molecular weight of ~26kDa. The GST protein of Asian corn borer is hydrophilic and may have a 30 amino acid signal peptide with a cleavage site between L30 and K31. A recombination vector pET28a-OfGST was constructed for purification and antibody preparation. Western blotting analysis showed that this protein reached the maximum expression level around 24 h in Asian corn borer larvae fed the plant toxin 2,4-dihydroxy-7-methoxy-1,4-benzoxazin-3-one. A second vector, htL4440-OfGST, was constructed to generate the dsRNA of the GST gene. A larval feeding bioassay showed that the expressed dsRNA significantly reduced the detoxification ability of Asian corn borer larvae and increased mortality rate up to 54%. Our data indicated that GST plays very important roles in detoxifying in Asian corn borer and can be used as an RNAi method to control this pest in the field.

The soil insect Bradysia odoriphaga (Diptera: Sciaridae) causes substantial damage to Chinese chive. Suitable reference genes in B. odoriphaga (Bradysia odoriphaga) have yet to be identified for normalizing target gene expression among samples by quantitative real-time PCR (qRT-PCR). This study was focused on identifying the expression stability of 12 candidate housekeeping genes in B. odoriphaga under various experiment conditions. The final stability ranking of 12 housekeeping genes was obtained with RefFinder, and the most suitable number of reference genes was analyzed by GeNorm. The results revealed that the most appropriate sets of internal controls were RPS15, RPL18, and RPS18 across developmental phases; RPS15, RPL28, and GAPDH across temperatures; RPS15 and RPL18 across pesticide treatments; RSP5, RPS18, and SDHA across photoperiods; ACTb, RPS18, and RPS15 across diets; RPS13 and RPL28 across populations; and RPS15, ACTb, and RPS18 across all samples. The use of the most suitable reference genes versus an arbitrarily selected reference gene resulted in significant differences in the analysis of a target gene expression. HSP23 in B. odoriphaga was found to be up-regulated under low temperatures. These results will contribute to the standardization of qRT-PCR and will also be valuable for further research on gene function in B. odoriphaga.

Abamectin has been used to control the diamondback moth, Plutella xylostella (P. xylostella), which is a major agricultural pest that can rapidly develop resistance against insecticides including abamectin. Although cytochrome P450 has been confirmed to play an important role in resistance in P. xylostella, the specific P450 genes associated with the resistance are unclear. The full-length cDNA of the cytochrome P450 gene CYP340W1 was cloned and characterized in the present study. The cDNA assembly yielded a sequence of 1929 bp, containing the open reading frame (ORF) 1491 bp and encodes a 496-amino acid peptide. CYP340W1 was expressed in all P. xylostella developmental stages but its expression level was highest in larvae and especially in the heads of larvae. The expression of CYP340W1 was significantly higher in an abamectin-resistant strain (ABM-R) than in its susceptible counterpart (ABM-S). In addition, expression of CYP340W1 was increased when the ABM-R strain was exposed to abamectin. When injected into third-stage ABM-R larvae, CYP340W1 dsRNA significantly reduced CYP340W1 expression at 6 h and reduced expression by 83% at 12 h. As a consequence of RNAi, the mortality of the injected abamectin-resistant larvae increased after a 48-h exposure to abamectin. The results indicate that the overexpression of CYP340W1 plays an important role in abamectin resistance in P. xylostella.

Arbuscular mycorrhizal fungi (AMF) protect host plants against diverse biotic and abiotic stresses and promote biodegradation of various contaminants. In this study effect of Glomus mosseae/Medicago sativa mycorrhiza on atrazine degradation was investigated. It was observed that the atrazine degradation rates with any addition level in mycorrhizal treatments were all significantly higher than those in non- mycorrhizal treatments. When atrazine was applied at 20 mg kg−1, the removal efficiency was up to 74.65%. Therefore, G. mosseae can be considered as ideal inhabitants of technical installations to facilitate phytoremediation. Furthermore, a total of 10.4 Gb was used for de novo transcriptome assembly, resulting in a comprehensive data set for the identification of genes corresponding to atrazine stress in the AM association. After comparative analysis with edgeR, a total of 2,060 differential expressed genes were identified, including 570 up-regulated genes and 1490 down-regulated genes. After excluding ‘function unknown’ and ‘general function predictions only’ genes, 172 up-regulated genes were obtained. The differentially expressed genes in AM association with and without atrazine stress were associated with molecular processes/other proteins, zinc finger protein, intracellular/extracellular enzymes, structural proteins, anti-stress/anti-disease protein, electron transport-related protein and plant growth associated protein. Our results not only prove AMF has important ecological significance on atrazine degradation but also provide evidence for the molecular mechanisms of atrazine degradation by AMF.

Based on fomesafen residue toxicity in soil, the strain FB5, which can utilize fomesafen as the sole carbon source, was isolated from a fomesafen-contaminated soybean field in Heilongjiang province, China. It was found to degrade 88.32% of 500mg/L fomesafen within 96h. Conbined with morphological, physiological, biochemical characteristics and 16S rDNA sequence, the strain was identified as Shigella flexneri. After evaluating the effects of environmental factors such as temperature, fomesafen concentration, and primary pH, the optimum growth conditions of the strain were obtained. A remarkable remediation ability of the strain to fomesafen–polluted soils was demonstrated by a sensitive crop bioassay in pot soil. This will provide a new suitable candidate for fomesafen biodegradation and a workable pathway for solving the hazards of fomesafen residues in agricultural soils.

In order to find new strains to degrade fomesafen in contaminated soil, we isolated and identified a high-efficiency degrading bacterium from polluted soil. The degrading characteristics and remediation ability of the strain were also studied.Characteristics of morphological, physiological, biochemical and 16S rRNA sequence were applied to identify the strain. The optimum growth conditions were obtained by studying the effect of environmental factors such as fomesafen concentration, primary pH and temperature on the strain. The strain's remediation ability to fomesafen-polluted soil was verified by sensitive crop and target weeds bioassay in pot soil.A high-efficiency degrading strain FB8 that used fomesafen as sole carbon source was isolated from soybean field suffering fomesafen in Heilongjiang province. It was initially identified as a member of the genus Pseudomonas. The strain could degrade 86.75% of 500 mg/L fomesafen within 96 h. Its optimal growth conditions were determined as follows: 500 mg/L fomesafen, primary pH between 6.0 and 8.0, and at 35 to 37 degrees C. The strain could remedy the sensitive crop maize and sorghum biomass after treating for 30 d for soil contaminated with 5 mg/kg of fomesafen.A fomesafen-degrading strain FB8 was selected from fomesafen-contaminated soil in Heilongjiang Province. The strain was closely related to Pseudomonas mendocina. The strain was a suitable candidate for bioremediation of fomesafen-contaminated soil.

To provide new atrazine-degrading strains for atrazine-polluted soil, we isolated the high-efficiency degradation bacterium from contaminated soil, identified with taxonomy, and studied the degrading characteristics and remediation capability of the strain in black soil.We used morphological, physiological and biochemical characteristics and 16S rDNA sequences analysis to identify the strain. We studied the effect of environmental factors such as incubation time, temperature and pH on the strain growth and atrazine degradation to confirm the optimum degradation conditions. The strain's degradation range was studied by using different herbicides as sole carbon and nitrogen source. The strain's remediation capability to atrazine-polluted soil was tested by sensitive crop bioassay after inoculating in pot soil.We isolated a high-efficiency degradation strain T3AB1 that used atrazine as sole carbon and nitrogen source from maize field suffering atrazine in Nehe, Heilongjiang province. It was initially identified as a member of the genus Arthrobacter sp.. The strain could degrade more than 99% of 500 mg/L atrazine (pH 8.0) within 72 h. We determined the best degradation conditions as follows: pH 7.0-8.0, 25-30 degrees C, 72-108 h. In addition, the strain used other herbicides as sole carbon and nitrogen source such as imazamox, imazethapyr, trifluralinm, clomazone and fomesafen, and the degradation rate reached 12.66% - 40.54% after 168 h. The strain could significantly remedy the sensitive rice crop biomass indexes after treating 21 days, and as time extending, its role in the remediation gradually increased.The screened atrazine-degrading strain T3AB1 could be a suitable candidate for bioremediation of atrazine-polluted soil.