Measurements of Intra- and Extra-Cellular 5-Methyltetrahydrofolate Indicate that DSM 20083 and DSM 20438 Do Not Actively Excrete 5-Methyltetrahydrofolate .

Certain intestinal bifidobacteria have the ability to synthesize folates. experiments revealed a high production, cellular accumulation, and release of reduced folate vitamers like 5-methyltetrahydrofolate and tetrahydrofolate in folate-free medium (FFM). However, it is still unclear to which extent synthesized folates are polyglutamylated and probably not available for transport, and if they are actively released by excretion. To address these questions, we characterized intra- and extra-cellular pteroylmonoglutamates and polyglutamylated 5-methyltetrahydrofolate (5-CH-HPteGlu) in DSM 20083 and DSM 20438. Folates were measured by means of stable isotope dilution assays (SIDA) coupled with LC-MS/MS analysis using [H]-5-methyltetrahydrofolic acid, [H]-tetrahydrofolic acid, and [H]-5-formyltetrahydrofolic acid as internal standards. Cell viability was examined by fluorescence microscopy. Quantitation of folate production by during the stationary phase revealed a linear increase of dead cells paralleled by increasing concentration of 5-formyltetrahydrofolate and 5-methyltetrahydrofolate (100% 5-CH-HPteGlu) in FFM, whereas the intracellular concentrations of these vitamers remained constant. After 24 h, (125 mg cells, wet weight) produced a total amount of 0.846 nmol 5-CH-Hfolate: 0.385 ± 0.059 nmol (46 ± 7%) and 0.461 ± 0.095 nmol (54 ± 11%) measured in the intracellular (viable cells; 52 ± 3% measured by fluorescence microscopy) and extracellular (lysed cells; 48 ± 3%) fraction, respectively. For (124 mg cells, wet weight), 1.135 nmol 5-CH-Hfolate was produced after 24 h, and a similar proportionality between intra- and extra-cellular folate concentrations and viable/lysed cells was observed. These results indicate that the strains tested produce and accumulate 5-CH-HPteGlu for cellular metabolism, and that extracellular concentrations of the vitamer arise from cell lysis.