2020
DOI: 10.1016/j.ijbiomac.2020.07.072
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Silver nanocomposites based on the bacterial fucose-rich polysaccharide secreted by Enterobacter A47 for wound dressing applications: Synthesis, characterization and in vitro bioactivity

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Cited by 33 publications
(48 citation statements)
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“…Thus, cultivation was performed under a fed-batch mode (feeding solution: Medium E* supplemented with 200 g/L of glycerol), with controlled temperature (30.0 ± 0.1 • C), pH (7.0 ± 0.02) and dissolved oxygen concentration (10% of the air saturation). FucoPol was recovered from the cultivation broth after 4 days as previously described [27]. The procedure involved dilution of the broth with deionized water (1:10, v/v) to reduce viscosity, centrifugation (13000×g, 45 min) for cell removal, thermal treatment (70 • C, 1 h) of the cell-free supernatant to promote protein denaturation and, finally, centrifugation (13,000× g, 45 min) for removal of cell fragments and denatured proteins.…”
Section: Fucopol Production Purification and Characterizationmentioning
confidence: 99%
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“…Thus, cultivation was performed under a fed-batch mode (feeding solution: Medium E* supplemented with 200 g/L of glycerol), with controlled temperature (30.0 ± 0.1 • C), pH (7.0 ± 0.02) and dissolved oxygen concentration (10% of the air saturation). FucoPol was recovered from the cultivation broth after 4 days as previously described [27]. The procedure involved dilution of the broth with deionized water (1:10, v/v) to reduce viscosity, centrifugation (13000×g, 45 min) for cell removal, thermal treatment (70 • C, 1 h) of the cell-free supernatant to promote protein denaturation and, finally, centrifugation (13,000× g, 45 min) for removal of cell fragments and denatured proteins.…”
Section: Fucopol Production Purification and Characterizationmentioning
confidence: 99%
“…The procedure involved dilution of the broth with deionized water (1:10, v/v) to reduce viscosity, centrifugation (13000×g, 45 min) for cell removal, thermal treatment (70 • C, 1 h) of the cell-free supernatant to promote protein denaturation and, finally, centrifugation (13,000× g, 45 min) for removal of cell fragments and denatured proteins. For FucoPol purification, the low molecular weight compounds (salts, glycerol, proteins) were removed by diafiltration in a cross-flow module (Sartocon Slide Holder), using a membrane with a surface area of 100 cm 2 and a 100 kDa nominal molecular weight cut-off (Hydrosart ultrafiltration cassette, Sartorius) [27]. During diafiltration, deionized water was added to the retentate to facilitate the diffusion of low molecular weight solutes across the membrane.…”
Section: Fucopol Production Purification and Characterizationmentioning
confidence: 99%
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“…Due to their high growth rates of microorganisms, to the possibility of enhancing productivity as well as customizing the biopolymers’ desirable properties by modifying the bioprocess conditions, the bacterial origin polysaccharides are of special interest in the scientific community [ 175 ]. Microbial polysaccharides are mainly exo-polysaccharides that bacteria secrete for their own purposes henceforth they do not provoke a biological response from cells, so they do not biologically interact with human tissues.…”
Section: Electrospun Nanofibers In Wound Healingmentioning
confidence: 99%