2). Suspensions were stored at −20°C until required. Liquid cultures were grown in starch–yeast extract (SY) broth that contained the following (in g l−1): soluble starch, 15; yeast extract (Difco), 1; K2HPO4 · 7H20, 1; NaCl, 3 (final pH adjusted to 7.2). Flasks (250 ml) that contained 50 ml of this media were inoculated with 0.1 ml of spore suspension and incubated at 30°C with shaking at 200 rpm. The fermentation media

were inoculated with 5% (v/v) of a preculture after 48 h growth and incubated at 30°C for 240 h under the standard condition of aeration and agitation (200 rpm). The fermentation basal media has the following composition (g/l): glucose 15, CaCO3 3, NaCl 3, MgSO4 0.5, (NH4)2HPO4 0.5, BAY 57-1293 cost K2HPO4 0.5, soya bean 1.0. The fermentation modified media has the follow composition (g/l): glucose 15, CaCO3 3, NaCl 3, MgSO4 0.5, (NH4)2HPO4 0.5, K2HPO4 0.5, l-tryptophan 0.5, Schiff base 0.5. After fermentation, the antibiotics of the broth were determined by extraction with n-butanol and ethyl acetate. The results were obtained by measuring absorbance at λmax = 364 nm (Hexaene H-85) and λmax = 252 nm (Azalomycine) with Perkin-Elmer Lambda 15 UV/VIS spectrophotometer (Vučetić et al., 1994; Karadžić et al., 1991). Growth was determined by measuring dry weights of cells. The broth was centrifuged

at 4000 rpm for 15 min to separate the mycelial biomass. After that biomass was dried at 105°C to constant weight and weighed. General

methods of preparation of Schiff bases Equimolar amounts of isatin and thiosemicarbazide, semicarbazide, and phenylhydrazine were dissolved selleck products in 95% ethanol. The solutions were heated under reflux for 1 h. The products were filtered, washed with ethanol, and dried in vacuum over CaCl2 (Konstantinović et al., 2007). The C59 wnt in vivo Structures of Schiff bases are given in Fig. 1. Fig. 1 Structures of Schiff bases Methods Microanalysis for carbon, hydrogen, and nitrogen was performed by using a Carlo Erba 1106 microanalyzer. The chloride content was determined potentiometrically. The melting points were determined by using Thomas–Hoover melting point apparatus and are uncorrected. FTIR spectra tuclazepam were recorded using a Michaelson Bomen MB-series spectrophotometer, using KBr pellet (1 mg/100 mg) technique. The electronic spectra were recorded on a Perkin/Elmer Lambda 15 UV/VIS spectrophotometer using 10−3 mol dm−3 solutions in DMF. 1H NMR spectra were obtained in DMSO solution with a Gemini-200 “HF NMR” spectrometer. Isatin-3-thiosemicarbazone (ITC) Yield 91.1%, Color Yellow. m.p. 239–241°C. IR (KBr, cm−1): 3470, 3304 ν(NH2), 3239, 3132 ν(NH), 1710 ν(C=O), 1585 ν(C=N), 1250 ν(C=S). UV/VIS (DMF, λ (nm/ε · 103(mol−1 dm3 cm): 349/0.946 π → π*, 366/1.325 π → π* 1H NMR (DMSO, δ, ppm) 6.9–7.7 (m, 4H, Ar), 8.69, 9.05 (s, 2H, NH2), 11.21 (2, 1H, NH), 12.47 (s, 1H, NH).