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Open Access Research

Substrate cycles in Penicillium chrysogenum quantified by isotopic non-stationary flux analysis

Zheng Zhao12, Angela ten Pierick1, Lodewijk de Jonge1, Joseph J Heijnen13 and S Aljoscha Wahl13*

Author Affiliations

1 Department of Biotechnology, Delft University of Technology, Julianalaan 67, Delft, 2628 BC, Netherlands

2 Current address: DSM Biotechnology Center, Alexander Fleminglaan 1, Delft, 2613 AX, Netherlands

3 Department of Biotechnology, Kluyver Centre for Genomics of Industrial Fermentation, Delft University of Technology, Julianalaan 67, Delft, 2628 BC, Netherlands

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Microbial Cell Factories 2012, 11:140  doi:10.1186/1475-2859-11-140

Published: 25 October 2012

Abstract

Background

Penicillium chrysogenum, the main production strain for penicillin-G, has a high content of intracellular carbohydrates, especially reduced sugars such as mannitol, arabitol, erythritol, as well as trehalose and glycogen. In previous steady state 13C wash-in experiments a delay of labeling enrichments in glycolytic intermediates was observed, which suggests turnover of storage carbohydrates. The turnover of storage pools consumes ATP which is expected to reduce the product yield for energy demanding production pathways like penicillin-G.

Results

In this study, a 13C labeling wash-in experiment of 1 hour was performed to systematically quantify the intracellular flux distribution including eight substrate cycles. The experiments were performed using a mixed carbon source of 85% CmolGlc/CmolGlc+EtOH labeled glucose (mixture of 90% [1-13C1] and 10% [U-13C6]) and 15% ethanol [U-13C2]. It was found, that (1) also several extracellular pools are enriched with 13C labeling rapidly (trehalose, mannitol, and others), (2) the intra- to extracellular metabolite concentration ratios were comparable for a large set of metabolites while for some carbohydrates (mannitol, trehalose, and glucose) the measured ratios were much higher.

Conclusions

The fast enrichment of several extracellular carbohydrates and a concentration ratio higher than the ratio expected from cell lysis (2%) indicate active (e.g. ATP consuming) transport cycles over the cellular membrane. The flux estimation indicates, that substrate cycles account for about 52% of the gap in the ATP balance based on metabolic flux analysis.