“…Phenotypic characteristics were tested as follows: each colony was aseptically transferred to a tube with MRS broth (Himedia, Mumbai, India) supplemented with 5% of glucose and an inverted Durham tube incubated at 30 °C for 48 h for test the gas production from glucose ( Potes and Marinho, 2007 ; Wu et al , 2012 ); after aliquots of the tube of gas production from glucose were tested for Gram reaction ( Oliveira et al , 2008 ; Silva et al , 2010 ). From this point the tests were performed following the sequence of classification according to the flowchart proposed ( Figure 1 ) and all the test were performed by aliquots of the test of gas production from glucose: catalase activity was tested by addition of hydrogen peroxide 3% ( Oliveira et al , 2008 ; Marty et al , 2012 ); growth at 10 °C for 7 days, and at 45 °C for 48 h, were tested in MRS broth with 0.02 g/L of bromocresol purple ( Hall et al , 2001 ; Potes and Marinho, 2007 ; Wu et al , 2012 ); growth in 18% NaCl added bromocresol purple 0.02 g/L at MRS broth were tested at 30 °C for 48 h ( Hall et al , 2001 ; Wu et al , 2012 ; growth at pH 4.4 e 4.5 in MRS broth adjusted to correct pH by the addition 1 M HCl ( Schillinger and Lücke, 1989 ) were incubated at 30 °C for 48 h; determination of lactic acid isomer formed (L, D or DL) was performed using an enzymatic-colorimetric kit (R-Biopharm, 11112821035, Darmstadt, Germany) according to the indication of the supplier. The reagents used were of analytical reagent grade.…”