Abstract

BackgroundThe soil bacterium Corynebacterium glutamicum, best known for its glutamate producing ability, is suitable as a producer of a variety of bioproducts. Glutamate is the precursor of the amino acid proline. Proline biosynthesis typically involves three enzymes and a spontaneous cyclisation reaction. Alternatively, proline can be synthesised from ornithine, an intermediate of arginine biosynthesis. The direct conversion of ornithine to proline is catalysed by ornithine cyclodeaminase. An ornithine overproducing platform strain with deletions of argR and argF (ORN1) has been employed for production of derived compounds such as putrescine. By heterologous expression of ocd this platform strain can be engineered further for proline production.ResultsPlasmid-based expression of ocd encoding the putative ornithine cyclodeaminase of C. glutamicum did not result in detectable proline accumulation in the culture medium. However, plasmid-based expression of ocd from Pseudomonas putida resulted in proline production with yields up to 0.31 ± 0.01 g proline/g glucose. Overexpression of the gene encoding a feedback-alleviated N-acetylglutamate kinase further increased proline production to 0.36 ± 0.01 g/g. In addition, feedback-alleviation of N-acetylglutamate kinase entailed growth-coupled production of proline and reduced the accumulation of by-products in the culture medium.ConclusionsThe product spectrum of the platform strain C. glutamicum ORN1 was expanded to include the amino acid L-proline. Upon further development of the ornithine overproducing platform strain, industrial production of amino acids of the glutamate family and derived bioproducts such as diamines might become within reach.

Highlights

  • The soil bacterium Corynebacterium glutamicum, best known for its glutamate producing ability, is suitable as a producer of a variety of bioproducts

  • Proline utilisation To establish if the putative proline degradation system of C. glutamicum had an effect on extracellular accumulation of proline, we first investigated the utilisation of proline as carbon and nitrogen source

  • Wild-type C. glutamicum was inoculated to an optical density (OD) of 1 in CGXII minimal medium with 20 g/L glucose or a C-equimolar concentration of proline as carbon source and 20 g/L ammonium sulfate and 5 g/L urea or a N-equimolar concentration of proline as nitrogen source

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Summary

Introduction

The soil bacterium Corynebacterium glutamicum, best known for its glutamate producing ability, is suitable as a producer of a variety of bioproducts. Glutamate is the precursor of the amino acid proline. Proline biosynthesis typically involves three enzymes and a spontaneous cyclisation reaction. The direct conversion of ornithine to proline is catalysed by ornithine cyclodeaminase. The amino acid functions as a compatible solute of C. glutamicum and in this respect the organism has Proline is synthesised from glutamate via three enzymatic and one spontaneous reactions, in most investigated microorganisms [4,9,10]. An alternative route to proline biosynthesis involves ornithine cyclodeaminase (OCD) which catalyses the conversion of ornithine to proline and ammonia with deamination of the α-amino group prior to cyclisation (Figure 1). The genome of C. glutamicum contains a putative ocd gene, evidence for its function as ornithine cyclodeaminase has not been reported [16]

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