2018
DOI: 10.1186/s13568-018-0683-3
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Lyoprotection and stabilization of laccase extract from Coriolus hirsutus, using selected additives

Abstract: The development of stable lyophilized laccase, obtained from Coriolus hirsutus, using a wide range of temperature treatments and storage conditions, was investigated. Using selected lyoprotectants, including, dextran 6 kDa, sucrose and a mixture of sodium benzoate, potassium sorbate and sorbitol (BKSS) (1.5:1.0:98.5; w/w/w) resulted by 2.4, 1.4 and 1.8-fold increase in laccase activity after lyophilization as compared to the fresh enzyme, respectively, whereas the addition of mannitol preserved 98.2% of its ac… Show more

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Cited by 5 publications
(2 citation statements)
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“…Refrigeration temperature is frequently to evaluate enzyme stability [ 31 , 73 ]. At 4.32 ± 1.22 °C (277.40 ± 1.32 K) rPOXA1B displayed a relative residual enzyme activity of 115.81% and a residual specific activity of 1045.58 ± 15.31 Umg − 1 ; which implies it was stable during the 12 months of the study ( Fig.…”
Section: Discussionmentioning
confidence: 99%
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“…Refrigeration temperature is frequently to evaluate enzyme stability [ 31 , 73 ]. At 4.32 ± 1.22 °C (277.40 ± 1.32 K) rPOXA1B displayed a relative residual enzyme activity of 115.81% and a residual specific activity of 1045.58 ± 15.31 Umg − 1 ; which implies it was stable during the 12 months of the study ( Fig.…”
Section: Discussionmentioning
confidence: 99%
“…Bagewadi et al, (2017) monitored Trichoderma harzianum HZN10 laccase fining a 45% enzyme activity loss in only 8 days of storage at 4 °C (277.15 K), [ 75 ]. Bou-Mitri and Kermasha, (2018) evaluated Coriolus hirsutus laccase, finding that after 4 weeks of storage at 4 °C (273.15 K) the residual enzyme activity was 8.5% [ 73 ]. rPOXA1B relative residual stability results in this study demonstrated an enzyme with high stability, exceeding that of other laccases, which makes it a promising enzyme for high scale use.…”
Section: Discussionmentioning
confidence: 99%