We report for the first time the isolation and identification of an alkaliphile that can grow on ferulic acid as the sole carbon source. VDH activity was detected in the cell extract from ferulic acid- or vanillin-grown cells, and the enzyme was purified and characterized. The characteristics of the purified enzyme were compared with another VDH purified from a previously isolated neutrophilic strain,

Burkholderia cepacia TM1 (Tanaka & Hirokane, 2000). This report is an important contribution to the investigation of ferulic acid and vanillin metabolism because there have been only a few studies on the enzymatic characteristics of VDH (Bare et al., 2002), and it adds to the genetic information on VDH orthologs available in the bacterial genome databases. Vanillin and vanillic acid (4-hydroxy-3-methoxybenzoic acid) were purchased from Wako Chemicals (Osaka, Japan). Ferulic acid [3-(4-hydroxy-3-methoxyphenyl) Cabozantinib concentration acrylic acid] was gifted by Tsuno Food Industrial Co. Ltd (Wakayama, Japan). Oxidized NAD+ and oxidized β-NADP+ were obtained from Oriental Yeast Co. Ltd (Osaka, Japan). Burkholderia cepacia TM1 was obtained from soil as described previously (Tanaka et al., 2001). Micrococcus sp. TA1 was recently isolated from an alkaline spa in Yamaguchi, Japan. Water or soil samples (about 0.1 g) were added to the medium, which comprised K2HPO4

(1 g L−1), (NH4)2SO4 (1 g L−1), yeast extract (1 g L−1), MgSO4·7H2O (0.1 g L−1), FeCl3·6H2O (0.02 g L−1), and ferulic acid (2 g L−1) or vanillin (2 g L−1). The pH of the medium was adjusted to 10 using 10% w/v Na2CO3 solution. Cultivation was performed for 5–7 days at 28 °C with shaking and repeated several times for enrichment. The HDAC inhibitor enrichment culture was spread on the above medium solidified with agar (15 g L−1). Single colonies obtained were picked out and inoculated into the above medium. Substrates and products were quantified by HPLC using an octyldodecylsilyl-silica gel column (TSK gel ODS80TM; Tosoh, Tokyo, Japan) as described previously (Mitsui et al., 2003). Protein concentration was determined using the Bradford method (Bradford, 1976) with bovine serum albumin as the standard. The relative molecular mass

of the native enzyme was determined by gel filtration Histamine H2 receptor using an HPLC system equipped with a TSK gel G3000SW column (Tosoh). The column was washed with 50 mM potassium phosphate buffer (KPB) (pH 7) containing 0.1 M NaCl. Standard protein markers were obtained from Oriental Yeast Co. Ltd (Tokyo, Japan). Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was performed on a 10% polyacrylamide gel (Laemmli, 1970), and Bio-Rad standard proteins (low range) were used for molecular mass measurement. The N-terminal and several internal amino acid sequences of the purified enzymes were determined using a protein sequencer (Applied Biosystems Japan, Tokyo, Japan) as described previously (Mitsui et al., 2007). Enzyme activity was measured using two methods.