Table 1. List of Metabolites Involved in Bioremediation along with Their Respective Chemical Shifts and Their Respective Fold Change as a Consequence of Uptake of Arsenic(III, V) Metal Uptakea,b.
relative
fold change |
||||
---|---|---|---|---|
metabolite name | assignment | chemical shifts (δ) in ppm | As(III) spiking vs control | As(V) spiking vs control |
Amino Acids | ||||
valine | γ-CH3 | 0.98 (d) | 4.1 | |
γ-CH3 | 1.03 (d)c | |||
proline | γ-CH2 | 2.00 (m)c | 1.3 | 2.3 |
1/2 β-CH2 | 2.06 (m) | |||
1/2 β-CH2 | 2.34 (m) | |||
glutamate | β-CH2 | 2.11 (m)c | 1.7 | 2.8 |
γ-CH2 | 2.34 (m) | |||
glutamine | β-CH2 | 2.12 (m) | 2.1 | |
γ-CH2 | 2.44 (m)c | |||
sacrosine | N–CH3 | 2.72 (s) | 1.3 | |
glycine | α-CH2 | 3.56 (s) | 2.2 | 3.0 |
cysteine | β-CH2 | 3.07 (m) | 1.8 | 2.5 |
α-CH | 3.97 (dd)c | |||
Organic Acids | ||||
glutarate | β,δ-CH2 | 2.16 (t) | 1.4 | |
succinate | α,β-CH2 | 2.39 (s) | 2.2 | |
citrate | 1/2 γ-CH2 | 2.52 (d)c | 2.7 | |
1/2 γ-CH2 | 2.69 (d) | |||
fumarate | CH | 6.51 (s) | 3.3 | 3.3 |
Carbohydrates/Sugar | ||||
sucrose | C10H | 3.46 (t) | 3.2 | 4.2 |
C12H | 3.55 (dd) | |||
C13H | 3.66 (s) | |||
C11H | 3.75 (m) | |||
C17H and C19H | 3.77 (m) | |||
C5H and C9H | 3.81 (dd) | |||
C4H | 4.04 (t) | |||
C3H | 4.21(d)c | |||
C7H | 5.40(d) | |||
α-glucose | C1H | 4.63 (d) | 2.7 | 5.1 |
β-glucose | C1H | 5.22 (d) | 3.4 | 5.3 |
Phosphagen | ||||
choline/PC | N–(CH3)3 | 3.20 (s) | 1.9 | 2.4 |
GPC | N–(CH3)3 | 3.22 (s) | 1.8 | 2.2 |
Osmolytes | ||||
glycerol | 1/2 γ-CH2 | 3.63 (d)c | 1.3 | 1.6 |
1/2 γ-CH2 | 3.65 (d) | |||
Nucleotides | ||||
ATP | C7H | 8.61 (s)c | 2.2 | 2.0 |
C12H | 8.25 (s) | |||
C2H | 6.13 (d) |
One-way analysis of variance (ANOVA) was conducted to determine significant (p < 0.001) metabolic changes. All differentially expressed metabolites involved in bioremediation pathway of As(III, V) are represented in bold. Metabolites that are specific to As(V) mitigation are marked with bold and italics.
All values of the metabolites were statistically significant with p value 0.001, respectively.
Metabolite peak used for evaluating the quantitative difference, as represented here by fold changes.