2010
DOI: 10.1016/j.molcatb.2010.06.012
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A novel silver-activated extracellular β-d-fructofuranosidase from Aspergillus phoenicis

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Cited by 16 publications
(30 citation statements)
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“…Considering soy bran as substrate, the maximal production was obtained after 72 hrs of growth using 1:0.5 (w/v) tap water to humidify this substrate (Figure 1). The production under such conditions was 30-times higher than that obtained under SbmF (Rustiguel et al 2010). According to Ashokkumar et al (2001) the maximal production of β-Dfructofuranosidase by Aspergillus niger under SSF was also obtained after 72 hrs.…”
Section: Production and Purification Of β-D-fructofuranosidasementioning
confidence: 66%
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“…Considering soy bran as substrate, the maximal production was obtained after 72 hrs of growth using 1:0.5 (w/v) tap water to humidify this substrate (Figure 1). The production under such conditions was 30-times higher than that obtained under SbmF (Rustiguel et al 2010). According to Ashokkumar et al (2001) the maximal production of β-Dfructofuranosidase by Aspergillus niger under SSF was also obtained after 72 hrs.…”
Section: Production and Purification Of β-D-fructofuranosidasementioning
confidence: 66%
“…Probably, soy bran offered additional nutrients improving the fungus development and also increasing the production of the enzyme. High levels of β-Dfructufuranosidase by A. phoenicis were also obtained under submerged fermentation, but using wheat bran as carbon source (Rustiguel et al 2010). The use of agroindustrial products or residues for SSF is an interesting alternative because it lowers cost for industries in the process of production of biomolecules, high recovery of the main product and availability of great variety of substrates.…”
Section: Production and Purification Of β-D-fructofuranosidasementioning
confidence: 99%
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“…Similar values were observed with extracellular β-fructofuranosidases produced by A. caespitosus and S. cerevisiae NRRLY12632 (Alegre et al, 2009;Mona and Mohamed, 2009). Most fungal β-fructofuranosidases have an optimum pH in the acidic range, as observed for A. phoenicis (Rustiguel et al, 2010) and C. sitophila PSSF84 (Patil et al, 2011) (both pH 4.5), and M. geophillus (pH 5.0) (Quershi et al, 2012). The FFase-I from A. versicolor is stable for 12 h between pH 3 and 6 (Figure 7b).…”
Section: Effect Of Ph On Enzyme Activity and Stabilitymentioning
confidence: 83%
“…However, at 65 and 70°C, the half-life decreased to 30 min. The FFase-I from A. versicolor had higher thermal stability when compared with β-fructofuranosidases produced by A. phoenicis, which was stable at 50°C for 1 h (Rustiguel et al, 2010), and A. caespitosus, which was stable at 60°C for 1 h and 20 min (Alegre et al, 2009). …”
Section: Effect Of Temperature On Enzyme Activity and Thermal Stabilitymentioning
confidence: 96%