2004
DOI: 10.1016/j.biochi.2004.08.005
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Comparison of physico-chemical characteristics of four laccases from different basidiomycetes

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Cited by 195 publications
(150 citation statements)
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“…1B) and Gel-filtration (data not shown), indicating a monomeric structure. This finding is consistent with typical fungal laccases, which are monomeric proteins of approximately 60-70 kDa, 34) such as Pleurotus eryngii (61 and 65 kDa), 35) Trametes hirsuta (70 kDa), 36) and Polyporus pinsitus (66 kDa). 37) Analytical isoelectric focusing revealed that Lac 1 is an acidic protein having a pI lower than 3.5.…”
Section: Molecular Mass and Pi Of Lacsupporting
confidence: 85%
“…1B) and Gel-filtration (data not shown), indicating a monomeric structure. This finding is consistent with typical fungal laccases, which are monomeric proteins of approximately 60-70 kDa, 34) such as Pleurotus eryngii (61 and 65 kDa), 35) Trametes hirsuta (70 kDa), 36) and Polyporus pinsitus (66 kDa). 37) Analytical isoelectric focusing revealed that Lac 1 is an acidic protein having a pI lower than 3.5.…”
Section: Molecular Mass and Pi Of Lacsupporting
confidence: 85%
“…Obviously, half-wave potentials registered in our studies ( Figure 3) coincide well with the redox potential of Trametes hirsuta Lc, measured to be 780 mV ± 10 mV versus NHE at pH about 6 [39,42]. We also noticed that the initial parts of both curves, 1 and 2, are almost identical, pointing to the fact that at low overpotentials, the bioelectrochemical reaction of O 2 reduction occurs in the kinetic mode, i.e.…”
Section: Time / Dayssupporting
confidence: 87%
“…The Lc was isolated and purified from a culture medium according to Ref. [39]. The homogeneous preparation of the enzyme, as judged from SDS-PAGE, with a protein concentration of about 15 mg mL -1 was stored in 100 mM phosphate buffer, pH 6.5 at -20°C.…”
Section: Enzymesmentioning
confidence: 99%
“…Nevertheless, currently applied incubation times of 30 and more minutes are too long to be economical. An important hindrance in reaction efficiency is its low redox-potential of the enzymes (Solomon et al 1992, Shleev et al 2004. Screening for mutations by modern molecular biological techniques can yield enzymes with higher redox-potential for recombinant production , Zumarraga et al 2007; further reading in Chapter 19 of this book).…”
Section: Homogenisationmentioning
confidence: 99%