Abstract

Production of biofuels via enzymatic hydrolysis of complex plant polysaccharides is a subject of intense global interest. Microbial communities are known to express a wide range of enzymes necessary for the saccharification of lignocellulosic feedstocks and serve as a powerful reservoir for enzyme discovery. However, the growth temperature and conditions that yield high cellulase activity vary widely, and the throughput to identify optimal conditions has been limited by the slow handling and conventional analysis. A rapid method that uses small volumes of isolate culture to resolve specific enzyme activity is needed. In this work, a high throughput nanostructure-initiator mass spectrometry (NIMS)-based approach was developed for screening a thermophilic cellulolytic actinomycete, Thermobispora bispora, for β-glucosidase production under various growth conditions. Media that produced high β-glucosidase activity were found to be I/S + glucose or microcrystalline cellulose (MCC), Medium 84 + rolled oats, and M9TE + MCC at 45°C. Supernatants of cell cultures grown in M9TE + 1% MCC cleaved 2.5 times more substrate at 45°C than at all other temperatures. While T. bispora is reported to grow optimally at 60°C in Medium 84 + rolled oats and M9TE + 1% MCC, approximately 40% more conversion was observed at 45°C. This high throughput NIMS approach may provide an important tool in discovery and characterization of enzymes from environmental microbes for industrial and biofuel applications.

Highlights

  • Saccharification of lignocellulosic feedstocks has great potential to provide fermentable sugars for production of renewable and potentially carbon neutral biofuels

  • We describe a method of screening T. bispora for β-glucosidase, a key glycoside hydrolase (GH) enzyme found in the cellulase mixtures that hydrolyzes cellobiose to glucose (Lynd et al, 2002), under various growth conditions by using acoustic printing coupled to nanostructure-initiator mass spectrometry (NIMS)

  • A method of screening T. bispora, a known cellulose degrader, for β-glucosidase production under various growth conditions using acoustic printing coupled to NIMS was developed

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Summary

Introduction

Saccharification of lignocellulosic feedstocks has great potential to provide fermentable sugars for production of renewable and potentially carbon neutral biofuels. Reports of optimal growth temperature (45–60◦C) and conditions that yield high cellulase activity vary widely (Liolios et al, 2010; Anderson et al, 2012). Methods are needed to determine optimal growth conditions for T. bispora that result in sufficient enzyme expression for activity analysis. These methods would be suitable for use of small volumes of isolate culture, could be performed on crude microbial cultures and would be suitable for resolving specific enzyme activities, most of which are based on spectroscopic properties changes of a substrate upon hydrolysis (Sharrock, 1988; Coleman et al, 2007, 2010; Dashtban et al, 2010)

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