Table 4. Effects of exogenous methionine on methyl cycle metabolites levels in M. oryzae Δmet6 mutants and wild type.
*nmoles.mg-1 dry weight | SAM | SAH | SAM/SAH |
---|---|---|---|
Wild type P1.2, MM | *0.27 ± 0.1 | 0.07 ± 0.02 | 3.85 |
Wild type P1.2, MM + Met | 0.35 ± 0.1 | 0.07 ± 0.02 | 4.85 |
Fold changes ** P12 + Met / P12 | 1.3 ° | 1 | 1.26 |
Δmet6 M15.1, MM + Met | 1.25 ± 0.3 | 0.45 ± 0.16 | 2.7 |
Δmet6 M22.1, MM + Met | 1.10 ± 0.17 | 0.30 ± 0.05 | 3.6 |
Δmet6 M23.1, MM + Met | 0.75 ± 0.1 | 0.35 ± 0.06 | 2.2 |
Fold changes ** Δmet6 / P1.2 | 3.0 ° | 5.3 ° | 0.56 |
Wild type M. oryzae isolate P1.2 was grown in liquid medium in absence (MM) or presence of 1 mM methionine (MM + Met) for 8 days. Δmet6 mutants (M15.1, M22.1 and M23.1) were grown in liquid MM supplemented with 1 mM methionine (MM + Met) for 8 days. SAM and SAH were quantified by HPLC as described in Materials and Methods. Data were expressed in nmoles.mg-1 dry weight and represent the mean ± standard deviation of 8 technical assays derived from three biological replicates.
Fold changes** (Δmet6 / P1.2 MM + Met) was calculated using average value of the three mutant lines over wild type.
°Differences are significant according to a t-test (5%).