• 한국미생물·생명공학회지
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• 제42권3호
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• pp.225-231
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• 2014

마늘낙엽버섯(Marasmius scorodonius)에 대하여 리그닌 분해 여부를 조사한 결과, 본 균주는 laccase를 생산하는 백색부후균으로 확인되었다. 마늘낙엽버섯 균사체로부터 laccase를 생산하기 위한 최적배지조건을 조사한 결과, 다양한 합성 배지 중에서 YM (1% dextrose, 0.5% malt extract, 0.3% yeast extract) 배지가 가장 높은 laccase 활성을 나타내었다. 또한 YM 배지의 조성 중에서 탄소원과 질소원을 각각 1% galactose와 0.4% yeast extract로 대체하였을 때 가장 높은 효소활성을 나타내었다. 본 균주는 최적배지조건에서 $25^{\circ}C$로 15일 동안 배양하였을 때 효소의 활성이 최대치에 도달함을 확인하였다. 균사체 배양 상등액을 Native-PAGE로 전기영동한 후 활성염색을 수행한 결과, 분자량 약 60-70 kDa 사이에서 laccase 활성을 가지는 2개의 밴드를 확인하였으며, 효소의 최적 pH와 온도는 각각 pH 3.4과 $75^{\circ}C$이었다.

• Journal of Microbiology and Biotechnology
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• 제27권6호
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• pp.1120-1127
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• 2017

Marasmius scorodonius secretes an extracellular laccase in potato dextrose broth, and this enzyme was purified up to 206-fold using $(NH_4)_2SO_4$ precipitation and a Hi-trap Q Sepharose column. The molecular mass of the purified laccase was estimated to be ~67 kDa by SDS-PAGE. The UV/vis spectrum of the enzyme was nontypical for laccases, and metal content analysis revealed that the enzyme contains 1 mole of Fe and Zn and 2 moles of Cu per mole of protein. The optimal pH for the enzymatic activity was 3.4, 4.0, and 4.6 with 2,2'-azino-bis(3-ethylbenzothazoline-6-sulfonate) (ABTS), guaiacol, and 2,6-dimethoxy phenol as the substrate, respectively. The optimal temperature of the enzyme was $75^{\circ}C$ with ABTS as the substrate. The enzyme was stable in the presence of some metal ions such as $Ca^{2+}$, $Cu^{2+}$, $Ni^{2+}$, $Mg^{2+}$, $Mn^{2+}$, $Ba^{2+}$, $Co^{2+}$, and $Zn^{2+}$ at a low concentration (1 mM), whereas $Fe^{2+}$ completely inhibited the enzymatic activity. The enzymatic reaction was strongly inhibited by metal chelators and thiol compounds except for EDTA. This enzyme directly decolorized Congo red, Malachite green, Crystal violet, and Methylene green dyes at various decolorization rates of 63-90%. In the presence of 1-hydroxybenzotriazole as a redox mediator, the decolorization of Reactive orange 16 and Remazol brilliant blue R was also achieved.