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. 2022 Jul 26:13:891870.
doi: 10.3389/fmicb.2022.891870. eCollection 2022.

Mechanism and kinetics of chlorpyrifos co-metabolism by using environment restoring microbes isolated from rhizosphere of horticultural crops under subtropics

Affiliations

Mechanism and kinetics of chlorpyrifos co-metabolism by using environment restoring microbes isolated from rhizosphere of horticultural crops under subtropics

Govind Kumar et al. Front Microbiol. .

Abstract

The indiscriminate use of organophosphate insecticide chlorpyrifos in agricultural crops causes significant soil and water pollution and poses a serious threat to the global community. In this study, a microbial consortium ERM C-1 containing bacterial strains Pseudomonas putida T7, Pseudomonas aeruginosa M2, Klebsiella pneumoniae M6, and a fungal strain Aspergillus terreus TF1 was developed for the effective degradation of chlorpyrifos. Results revealed that microbial strains were not only utilizing chlorpyrifos (500 mg L-1) but also coupled with plant growth-promoting characteristics and laccase production. PGP traits, that is, IAA (35.53, 45.53, 25.19, and 25.53 μg mL-1), HCN (19.85, 17.85, 12.18, and 9.85 μg mL-1), and ammonium (14.73, 16.73, 8.05, and 10.87 μg mL-1) production, and potassium (49.53, 66.72, 46.14, and 52.72 μg mL-1), phosphate (52.37, 63.89, 33.33, and 71.89 μg mL-1), and zinc (29.75, 49.75, 49.12, and 57.75 μg mL-1) solubilization tests were positive for microbial strains T7, M2, M6, and TF1, respectively. The laccase activity by ERM C-1 was estimated as 37.53, 57.16, and 87.57 enzyme U mL-1 after 5, 10, and 15 days of incubation, respectively. Chlorpyrifos degradation was associated with ERM C-1 and laccase activity, and the degree of enzyme activity was higher in the consortium than in individual strains. The biodegradation study with developed consortium ERM C-1 showed a decreased chlorpyrifos concentration from the 7th day of incubation (65.77% degradation) followed by complete disappearance (100% degradation) after the 30th day of incubation in the MS medium. First-order degradation kinetics with a linear model revealed a high k -day value and low t 1/2 value in ERM C-1. The results of HPLC and GC-MS analysis proved that consortium ERM C-1 was capable of completely removing chlorpyrifos by co-metabolism mechanism.

Keywords: ERM C-1; biodegradation; chlorpyrifos; consortium; plant growth promotion.

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Conflict of interest statement

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Figures

FIGURE 1
FIGURE 1
Different plant growth-promoting properties of rhizobacterial and fungal strains. The results were the average of five replicates (n = 5). Bars represent standard error. Significant differences based on the analysis variance (ANOVA) are shown by different letters above the error bars, followed by the post-hoc DMRT test (p ≤ 0.05) using the software SPSS.
FIGURE 2
FIGURE 2
Laccase activity by individual strains and developed consortium. The results were the average of five replicates (n = 5). Bars represent the standard error. Significant differences based on the analysis variance (ANOVA) are shown by different letters above the error bars, followed by the post-hoc DMRT test (p ≤ 0.05) using the software SPSS.
FIGURE 3
FIGURE 3
Chlorpyrifos biodegradation in different media at different time intervals. Data were the average of five replicates (n = 5). Bars represent standard error. Significant differences based on the analysis variance (ANOVA) are shown by different letters above the error bars, followed by the post-hoc DMRT test (p ≤ 0.05) using the software SPSS.
FIGURE 4
FIGURE 4
(A) Dehydrogenase activity of the soil treated by different strains and developed consortium in sterile and natural conditions. The recorded data were the average of five replicates (n = 5). Bars represent the standard error. Significant differences based on the analysis variance (ANOVA) are shown by different letters above the error bars, followed by the post-hoc DMRT test (p ≤ 0.05) using the software SPSS. (B) Fluorescein diacetate (FDA) hydrolysis activity of the soil treated with different strains and developed consortium in sterile and natural conditions. The recorded data were the average of five replicates (n = 5). Bars represent standard error. Significant differences based on the analysis variance (ANOVA) are shown by different letters above the error bars, followed by the post-hoc DMRT test (p ≤ 0.05) using the software SPSS.
FIGURE 5
FIGURE 5
Heat map analysis of chlorpyrifos biodegradation by individual strains and developed consortium (ERM C-1) at different time intervals.
FIGURE 6
FIGURE 6
(A) Schematic diagram of the impact of pesticide (chlorpyrifos) and microbes (ERM- environment restoring microbes-C-1 formulation and already exited microbes) on soil, plant, and environment. (B) Mechanisms of action of bio-surfactant producing environment restoring microbes (ERM) in chlorpyrifos (CHL) biodegradation.

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