Abstract

In the present work, four derivatives of salicylaldehyde (salicylaldehyde-hydrazone, phenylhydrazone, semicarbazone and thiosemicarbazone) were synthesized using both conventional (95% ethanol) and green (crude glycerol from biodiesel production) solvents. The obtained compounds were identified by elemental microanalysis, as well as FTIR, UV/Vis and 1H-NMR spectroscopic methods. Yields of 93?98% of the compounds in crude glycerol were achieved within 10?25 min. The derivatives of salicylaldehyde and crude glycerol were used as a nitrogen and carbon source, respectively, in the medium for antibiotic (hexaene H-85 and azalomycine B) production by Streptomyces hygroscopicus CH-7. The highest concentrations of hexaene H-85 and azalomycine B were achieved in the medium containing salicylaldehyde-thiosemicarbazone (198 and 69 ?g/cm3, respectively). Derivatives of salicylaldehyde also impacted the strain morphology. In the media with salicylaldehyde- phenylhydrazone and salicylaldehyde-thiosemicarbazone, S. hygroscopicus CH-7 grew like large dispersive pellets with long twisted filaments that produced the highest yield of the antibiotics.

Highlights

  • In the present work, four derivatives of salicylaldehyde were synthesized using both conventional (95% ethanol) and green solvents

  • Several derivatives of salicylaldehyde were synthesized in crude glycerol that originated from the alkali-catalyzed transesterification of edible sunflower oil as well as in ethanol (95 vol.%) as a conventional solvent The main goal was to increase the product yield and to shorten the reaction time, as well as to evaluate the obtained derivatives as a nitrogen source in the nutrition medium in antibiotic production by S. hygroscopicus CH-7

  • Dard solvent 95% ethanol, and in crude glycerol, a green solvent obtained as a byproduct of the biodiesel production

Read more

Summary

Introduction

Four derivatives of salicylaldehyde (salicylaldehyde-hydrazone, phenylhydrazone, semicarbazone and thiosemicarbazone) were synthesized using both conventional (95% ethanol) and green (crude glycerol from biodiesel production) solvents. Several derivatives of salicylaldehyde (salicylaldehyde-hydrazone, salicylaldehyde-phenylhydrazone, salicylaldehyde-semicarbazone and salicylaldehyde-thiosemicarbazone) were synthesized in crude glycerol that originated from the alkali-catalyzed transesterification of edible sunflower oil as well as in ethanol (95 vol.%) as a conventional solvent The main goal was to increase the product yield and to shorten the reaction time, as well as to evaluate the obtained derivatives as a nitrogen source in the nutrition medium in antibiotic production by S. hygroscopicus CH-7. The reaction occurred without the use of catalyst at 80 °C, and compared to the conventional solvent, the reaction times were shorter and the yields of salicyladehyde derivatives were higher (∆ = 2– 8%), Table 1.

Results
Conclusion
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call