1 Department of Microbiology, Guru Nanak Dev University, Amritsar, Punjab, 143005, India.
2 Department of Chemical and Biological Engineering, South Dakota School of Mines and Technology, Rapid City, SD, 57701, USA; Composite and Nanocomposite Advanced Manufacturing Center - Biomaterials [CNAM/Bio], Rapid City, SD, 57701, USA; BuG ReMeDEE Consortium, South Dakota School of Mines and Technology, Rapid City, SD, 57701, USA.
3 Center for Structural and Functional Genomics, Concordia University, 7141, Sherbrooke Street, West, Montreal, Quebec, H4B 1R6, Canada.
4 Department of Microbiology, Guru Nanak Dev University, Amritsar, Punjab, 143005, India. Electronic address: chadhabs@yahoo.com.

A novel Lytic Polysaccharide Monooxygenase (LPMO) family AA9 (PMO9A_MALCI) protein from thermophilic fungus Malbranchea cinnamomea was cloned and expressed in Pichia pastoris. The expressed protein was purified to homogeneity using ion exchange and hydrophobic interaction chromatography. SDS-PAGE analysis showed PMO9A_MALCI to be ~27 kDa protein. High performance anion exchange chromatography and mass spectrometry confirmed that purified protein was active against an array of cellulosic (avicel, carboxy methyl cellulose) and hemicellulosic (birch wood xylan, wheat arabinoxylan and rye arabinoxylan) substrates, releasing both oxidized and unoxidized cello-oligosaccharide and xylo-oligosaccharide products respectively. Presence of double oxidized products during mass spectrometric analysis as well as in-silico analysis confirmed that the expressed protein belongs to Type 3 LPMO family. Molecular dynamic simulations further confirmed the sharing of common amino acid residues conserved for catalysis of both cellulosic and hemicellulosic substrates which further indicates that both substrates are equally preferred. Enzymatic cocktails constituted by replacing a part of commercial cellulase CellicCTec2 with PMO9A_MALCI (9:1/8:2) led to synergistic improvement in saccharification of acid and alkali pretreated biomass. This is the first report on heterologous expression of LPMO from M. cinnamomea, exhibiting catalysis of cellulose and pure xylan.