0, 200 μl of CFE and 50 μl of 20 mM o-nitrophenilgalactopiranoside (ONPG). The mixture was immediately incubated at 37°C and absorbance was measured (λ = 420 nm).

Each condition was assayed independently by triplicate and the values were standardized to protein contents of cell extracts, determined by using the BCA Protein Assay Reagent Kit (Pierce, Trichostatin A research buy Rockford, Ill.). Overexpression of tyrS and immunodetection The gene encoding for TyrS was amplified using primers TYSF and TYSR (Table 2) and cloned into a pNZcLIC expression vector using the VBEx system [45], yielding the corresponding derivative pNZcTyrS. For detection purposes, a decaHis-tag was added to the C-terminal of the learn more target protein. tyrS expression was carried using the NICE system [46]. The genes encoding nisR and nisK were introduced in E. durans IPLA655 in the low copy number plasmid pNZ9530 [40]. After induction with 2 μg L-1 nisin, expression of the protein was confirmed by Western blotting analysis of cell lysates

by 10% SDS-PAGE electrophoresis gels, subsequently electroblotted and immunodetected with an anti-His-tag antibody (Amersham Pharmacia Biotech Inc. Piscataway). Chemiluminescence Fedratinib in vitro detection was done using the Western-Light kit (Tropix Inc. Bedford, MA) and quantified using the Fujifilm LAS-3000 imaging system (Fuji Photo Film Co. Ltd; Tokyo). Analysis of tyramine by HPLC The quantitative analysis of tyramine production was undertaken by reverse-phase high performance liquid chromatography (RP-HPLC) using a Waters liquid chromatograph controlled by Millenium 32 Software (Waters, Milford, MA, USA). The samples were prepared by centrifugation at 8,000 × g for 10 min. The resulting supernatants were filtered

isometheptene using Millipore 0.2 μm filters and derivatized using dabsyl chloride, as described by Krause et al. [47]. Separations were performed using a Waters Nova-pack C18 column (150 × 3.9 mm). Usually, 10 μl of the derivatized sample was injected and detection performed at 436 nm. The solvent gradient and detection conditions were similar to those described by Krause et al. [47]. Acknowledgements This research was performed with financial support from the Ministry of Science and Innovation, Spain (AGL2010-18430) and the European Community’s Seventh Framework Programme (BIAMFOOD-211441). We are grateful to Paloma López for technical assistance with Primer Extension experiments, and Begoña Redruello for experienced support provided for protein modelling and structure alignment. Strain L. lactis NZ9000 and plasmid pNZ9530 were kindly provided by NIZO food research, and plasmids pILORI4 and pNZcLIC were kindly provided by Oscar Kuipers and Bert Poolman, respectively. D. M. Linares is the recipient of a contract from Gobierno del Principado de Asturias. B. del Río is beneficiary of a JAE DOC contract (CSIC). References 1.