Abstract

Mycofactocin (MFT) is a recently discovered glycosylated redox cofactor, which has been associated with the detoxification of antibiotics in pathogenic mycobacteria, and, therefore, of potential medical interest. The MFT biosynthetic gene cluster is commonly found in mycobacteria, including Mycobacterium tuberculosis, the causative agent of tuberculosis. Since the MFT molecule is highly interesting for basic research and could even serve as a potential drug target, large-scale production of the molecule is highly desired. However, conventional shake flask cultivations failed to produce enough MFT for further biochemical characterization like kinetic studies and structure elucidation, and a more comprehensive study of cultivation parameters is urgently needed. Being a redox cofactor, it can be hypothesized that the oxygen transfer rate (OTR) is a critical parameter for MFT formation. Using the non-pathogenic strain Mycobacterium smegmatis mc2 155, shake flask experiments with online measurement of the oxygen uptake and the carbon dioxide formation, were conducted under different levels of oxygen supply. Using liquid chromatography and high-resolution mass spectrometry, a 4–8 times increase of MFT production was identified under oxygen-limited conditions, in both complex and mineral medium. Moreover, the level of oxygen supply modulates not only the overall MFT formation but also the length of the glycosidic chain. Finally, all results were scaled up into a 7 L stirred tank reactor to elucidate the kinetics of MFT formation. Ultimately, this study enables the production of high amounts of these redox cofactors, to perform further investigations into the role and importance of MFTs.

Highlights

  • The genus Mycobacterium comprises the highly important etiological agents for human tuberculosis (Mycobacterium tuberculosis), bovine tuberculosis (M. bovis), and leprosy (M. leprae) (Gupta et al, 2018; Parte, 2018)

  • Oxygen supply is likely a key factor influencing redox cofactor synthesis, most of the published screening experiments with mycobacteria were performed in a shake flask providing no information on oxygen supply

  • M. smegmatis mc2 155 cultivations were performed in a Transfer-Rate Online Measurement (TOM) device which enables online measurement of oxygen uptake and carbon dioxide formation (Figure 2)

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Summary

Introduction

The genus Mycobacterium comprises the highly important etiological agents for human tuberculosis (Mycobacterium tuberculosis), bovine tuberculosis (M. bovis), and leprosy (M. leprae) (Gupta et al, 2018; Parte, 2018). Invitro studies on TB pathogenesis, mycobacterial physiology, as well as as the development of novel treatments, are complicated by the high level of biosafety and the low duplication rate of the pathogen, requiring up to 4 weeks to develop visible colonies on agar plates. For this reason, the non-pathogenic strain Mycolicibacterium smegmatis mc 155 (synonym Mycobacterium smegmatis) can be a suitable model (Reyrat and Kahn, 2001; Shiloh and Champion, 2010; Yamada et al, 2018)

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