Abstract

BackgroundPleurotus ostreatus is the second edible mushroom worldwide, and a model fungus for delignification applications, with the advantage of growing on woody and nonwoody feedstocks. Its sequenced genome is available, and this gave us the opportunity to perform proteomic studies to identify the enzymes overproduced in lignocellulose cultures.ResultsMonokaryotic P. ostreatus (PC9) was grown with poplar wood or wheat straw as the sole C/N source and the extracellular proteins were analyzed, together with those from glucose medium. Using nano-liquid chromatography coupled to tandem mass spectrometry of whole-protein hydrolyzate, over five-hundred proteins were identified. Thirty-four percent were unique of the straw cultures, while only 15 and 6 % were unique of the glucose and poplar cultures, respectively (20 % were produced under the three conditions, and additional 19 % were shared by the two lignocellulose cultures). Semi-quantitative analysis showed oxidoreductases as the main protein type both in the poplar (39 % total abundance) and straw (31 %) secretomes, while carbohydrate-active enzymes (CAZys) were only slightly overproduced (14–16 %). Laccase 10 (LACC10) was the main protein in the two lignocellulose secretomes (10–14 %) and, together with LACC2, LACC9, LACC6, versatile peroxidase 1 (VP1), and manganese peroxidase 3 (MnP3), were strongly overproduced in the lignocellulose cultures. Seven CAZys were also among the top-50 proteins, but only CE16 acetylesterase was overproduced on lignocellulose. When the woody and nonwoody secretomes were compared, GH1 and GH3 β-glycosidases were more abundant on poplar and straw, respectively and, among less abundant proteins, VP2 was overproduced on straw, while VP3 was only found on poplar. The treated lignocellulosic substrates were analyzed by two-dimensional nuclear magnetic resonance (2D NMR), and a decrease of lignin relative to carbohydrate signals was observed, together with the disappearance of some minor lignin substructures, and an increase of sugar reducing ends.ConclusionsOxidoreductases are strongly induced when P. ostreatus grows on woody and nonwoody lignocellulosic substrates. One laccase occupied the first position in both secretomes, and three more were overproduced together with one VP and one MnP, suggesting an important role in lignocellulose degradation. Preferential removal of lignin vs carbohydrates was shown by 2D NMR, in agreement with the above secretomic results.Electronic supplementary materialThe online version of this article (doi:10.1186/s13068-016-0462-9) contains supplementary material, which is available to authorized users.

Highlights

  • Pleurotus ostreatus is the second edible mushroom worldwide, and a model fungus for delignification applications, with the advantage of growing on woody and nonwoody feedstocks

  • A total of 241, 391, and 206 extracellular proteins were identified in the poplar, wheat straw, and HAT fungal cultures, respectively, as summarized in Fig. 1, where the numbers of unique proteins are indicated together with those shared by the three secretomes or only by two of them

  • Conclusions some differences were observed between the two substrates, the secretome of P. ostreatus growing both on poplar wood and wheat straw was characterized by a strong overproduction of lignin-modifying enzyme (LME) with respect to glucose medium

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Summary

Introduction

Pleurotus ostreatus is the second edible mushroom worldwide, and a model fungus for delignification applications, with the advantage of growing on woody and nonwoody feedstocks. The genomes of other Polyporales were sequenced, such as: (i) Postia placenta [5], as a model causing agent of the so-called brown-rot decay of wood (due to its brownish color after polysaccharide removal) [4]; and (ii) Ceriporiopsis subvermispora [6], a white-rot fungus of biotechnological interest due to its selective degradation of lignin [7]. With the availability of massive sequencing tools, many other Agaricomycotina genomes were sequenced up to a total of 126 available (on 31 September 2015) at the Mycocosm portal (http:// www.genome.jgi.doe.gov/programs/fungi) of the DOE Joint Genome Institute (JGI) [8] Using this genomic information, several recent studies have discussed the genes involved in lignocellulose decay in saprotrophic basidiomycetes often in combination with transcriptomic and secretomic analyses [9,10,11,12,13,14,15], they were still largely based on Polyporales species

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