Isolation, purification, and characterization of novel melanin from the submerged fermentation of Rhizobium radiobacter

In this study, a novel water-insoluble bacterial melanin was first isolated and purified from the fermentation culture of Gram-negative bacterial Rhizobium radiobacter ATCC 1333 through the thermal acid-alkali treatment. The highest extracellular melanin production was 3.46 +/- 0.07 g.L- 1 when the initial glutamic acid concentration was 10 g.L- 1. The molecular weight of the purified bacterial melanin (TPBM) was 686 g/mol. The molecular formula (C34H30N4O12) and chemical structure were defined based on FT-IR, MALDI-TOF/MS, Py-GC/MS NMR (1H and 13C), and elemental analyses. Furthermore, UV-vis spectroscopy results indicated that TPBM showed maximum absorption at around 222 nm. TPBM was easily soluble in alkaline solutions, but hardly-soluble in aqueous and majority of the organic solvents. In addition, TPBM was stable to temperature, light, reducing agent, and most metal ions. However, TPBM could be bleached when subjected to the action of oxidants and precipitated with FeCl3 and AgNO3. TPBM (50 mu g.mL- 1) possessed high DPPH free radical (89.74% +/- 1.10%) and hydroxyl scavenging properties (84.12% +/- 1.31%). Finally, TPBM displayed potential anti-bacterial properties against E. coli, S. aureus, A. baumanii, and M. albican. These results provided a theoretical basis for the later development and utilization of TPBM.

Automated summary

In this study, a novel water-insoluble bacterial melanin, named TPBM, was isolated and purified from the fermentation culture of Gram-negative bacterial Rhizobium radiobacter ATCC 1333 through thermal acid-alkali treatment. TPBM exhibited high DPPH free radical and hydroxyl scavenging properties, as well as potential antibacterial properties.