Resumo

REVOLLO ESCUDERO, Enrique Luis; SERNA DAZA, Oriana Danuta  e  HERNANDEZ TORRES, Jorge. Characterization of lignocellulose-degrading rare actinobacteria: demostration of laccase activity in two isolates of Tsukamurella sp and Cellulosimicrobium sp. Rev. colomb. biotecnol [online]. 2012, vol.14, n.2, pp.70-80. ISSN 0123-3475.

The physicochemical characteristics of lignin and its compaction with cellulose have restricted the biotechnological exploitation of enormous amounts of plant biomass. Laccases are a subfamily of multicopper oxidases involved in lignin depolymerization. Although they have been extensively characterized in fungi, studies of the diversity and functions of laccases in prokaryotes are mainly on enzyme isoforms of Streptomyces sp. In this work we isolated 20 strains of soil actinomycetes. The laccase activity of 17 of them was evidenced in qualitative assays with guaiacol, and two selected strains were characterized in detail. The morphological evidence and the analysis of the 16S rRNA gene sequences suggest that these two isolates belong to the genera Tsukamurella and Cellulosimicrobium. In submerged cultures with shaking, AC01 (Tsukamurella sp.) exhibited a maximal oxidation activity of ABTS (2,2 '-azino-bis-(3-ethylbenzthiazoline-6-sulfonate) of 108 U/L. On the other hand, AC18 (Cellulosimicrobium sp.) that exhibited a higher oxidative activity of guaiacol than the other 16 isolated strains and showed resistance to toxic levels of copper, reached a maximum ABTS oxidation rate of 0.56 U/L. These results suggest that in AC18 operates a mechanism of substrate or inducer specificity, regulating the measurable laccase activity and laccase gene expression. Genomic and functional characterization of laccases of new ligninolytic actinomycetes may help to extend the range of redox centers with specific biotechnological applications, as well as establishing their evolutionary relationships with eukaryotes.

Palavras-chave : Actinobacteria; delignification; lignin-modifying enzymes; EC 1.10.3.2; ABTS.

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