% 02 when phosphate medium was used, and 02 + CO2 (95:5) with media based on bicarbonate. Incubations (in duplicate) were carried out for 2 hr. at 390 with a shaking rate of 100 strokes/min. Krebs-Ringer phosphate and Krebs-Ringer bicarbonate media were prepared as described by Umbreit, Burris & Stauffer (1957). Results were expressed as umc (or pmoles or mg.)/hr./g. of tissue (,umc/hr./g_). Purification of substrates. After distillation AnalaR-grade acetic acid, propionic acid and n-butyric acid (British Drug Houses Ltd.) were found to be homogeneous when examined by gas-liquid partition chromatography (James & Martin, 1952). Aqueous solutions of these substrates were neutralized (pH 7-0) with NaOH and stored at-10°. Radioactive substrates. The sodium salts of [1-14C]acetic acid, [2-_4C]acetic acid, [1_14C]propionic acid, [2_14C]_ propionic acid and [1-14C]butyric acid, and NaH14CO3, were obtained from The Radiochemical Centre, Amersham, Bucks. Sodium [2-_4C]butyrate and sodium [3_14C]butyrate were purchased from California Foundation for Biochemical Research, Calif., U.S.A. The radioactivity of labelled substrates was checked by wet oxidation (Van Slyke & Folch, 1940) to C02, which was assayed as BaCO3 by the procedure described by Annison & White (1961). Leuconostoc mesenteroides. A culture of this organism (strain 39