Abstract

Glucose 6-phosphate is the phosphorylated form of glucose and is used as a reagent in enzymatic assays. Current production occurs via a multi-step chemical synthesis. In this study we established a fully enzymatic route for the synthesis of glucose 6-phosphate from cellulose. As the enzymatic phosphorylation requires ATP as phosphoryl donor, the use of a cofactor regeneration system is required. We evaluated Escherichia coli glucokinase and Saccharomyces cerevisiae hexokinase (HK) for the phosphorylation reaction and Pseudomonas aeruginosa polyphosphate kinase 2 (PPK2) for ATP regeneration. All three enzymes were characterized in terms of temperature and pH optimum and the effects of substrates and products concentrations on enzymatic activities. After optimization of the conditions, we achieved a 85% conversion of glucose into glucose 6-phosphate using the HK/PPK2 activities within a 24 h reaction resulting in 12.56 g/l of glucose 6-phosphate. Finally, we demonstrated the glucose 6-phosphate formation from microcrystalline cellulose in a one-pot reaction comprising Aspergillus niger cellulase for glucose release and HK/PPK2 activities. We achieved a 77% conversion of released glucose into glucose 6-phosphate, however at the expense of a lower glucose 6-phosphate yield of 1.17 g/l. Overall, our study shows an alternative approach for synthesis of glucose 6-phosphate that can be used to valorize biomass derived cellulose.

Highlights

  • Glucose 6-phosphate is the phosphorylated form of glucose and is an essential reagent in enzymatic assays, for example to determine glucose 6-phosphate dehydrogenase (G6PDH) activity in patients that suffer from G6PDH deficiency

  • Enzymatic phosphorylation of glucose using either hexokinases or glucokinases requires the cofactor ATP as phosphoryl donor and the use of a cofactor regeneration system is required for production of glucose 6-phosphate at larger scale

  • We evaluated two different enzymes for the phosphorylation of glucose, a commercially available yeast hexokinase (HK) preparation and E. coli glucokinase (EGlk)

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Summary

Introduction

Glucose 6-phosphate is the phosphorylated form of glucose and is an essential reagent in enzymatic assays, for example to determine glucose 6-phosphate dehydrogenase (G6PDH) activity in patients that suffer from G6PDH deficiency. Biological production of glucose 6-phosphate could be achieved via two approaches, fermentation or enzymatic biosynthesis. Glucose 6-phosphate is an essential metabolite in the central carbon metabolism at the crossroad of glycolysis and the pentose phosphate pathway (Wilson, 1995, 2003). Metabolites in the central carbon metabolism are consumed within seconds and do not accumulate. Cellular membranes are impermeable for the negatively charged glucose 6-phosphate and other sugar phosphates and no specific transporters for these compounds exist in cells precluding excretion. Processes for enzymatic production of sugar-phosphates, such as xylulose-5-phosphates, 2-deoxyribose 5-phosphate or fructose 1,6-bisphosphate, have been established

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