“…; Table ). In order to characterize bacterial colonies, the strains were grown on nonselective media YPGA, and two semiselective media used routinely to identify Cmm, CMM1 (10 g L −1 sucrose, 3.32 g L −1 Tris base, 11.44 g L −1 Tris.HCl, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 5 g L −1 LiCl, 2 g L −1 yeast extract, 1 g L −1 NH 4 Cl, 4 g L −1 casein hydrolysate, 15 g L −1 agar, 10 mg L −1 polymyxin B sulphate, 28 mg L −1 nalidixic acid, 100 mg L −1 nystatin) and SCM (10 g L −1 sucrose, 2 g L −1 K 2 HPO 4 , 0.5 g L −1 KH 2 PO 4 , 1.5 g L −1 H 3 BO 3 , 0.1 g L −1 yeast extract, 0.25 g L −1 Mg 2 SO 4 .7H 2 O, 1.5 g L −1 boric acid, 18 g L −1 agar, 100 mg L −1 nicotinic acid, 30 mg L −1 nalidixic acid, 10 mg L −1 potassium tellurite, 200 mg L −1 cycloheximide) (Fatmi & Schaad, ) media at 28 °C for 3, 5 and 7 days, respectively. Cultures of each strain were grown in YPGB (5 g L −1 yeast extract, 5 g L −1 bactopeptone, 10 g L −1 glucose) medium to keep as stocks using 20% glycerol at −20 and −80 °C.…”