Sequential C1 fermentation - Converting CO2 into L-glutamate, 3-hydroxypropionate or mevalonate using Acetobacterium woodii and Corynebacterium glutamicum
Christina Goldbeck, Felix Gaile, Tom Seitz, Annika Renner, Camilla Ullmann, Petra Dangel, Florian Kirschner, Daniel Siebert, Frank R. Bengelsdorf, Bernhard J. Eikmanns, Andreas Schwentner
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引用次数: 0
Abstract
We here apply sequential microbial bioprocesses by combining the acetate-producing features of Acetobacterium woodii from C1 substrates and the ability of Corynebacterium glutamicum to grow and to form value-added products from acetate. In a first fermentation, we demonstrate production of up to 400 mM bio-acetate with A. woodii from either CO2 plus H2 or from methanol under anaerobic conditions. In a subsequent cultivation, we employed C. glutamicum to convert the acetogen-derived bio-acetate into the amino acid L-glutamate (up to 13.1 mM = 1.93 g L−1), or the heterologous products 3-hydroxypropionate (up to 40.8 mM = 3.68 g L−1) and mevalonate (up to 11.3 mM = 1.67 g L−1). The sequential fermentation platform presented here thus allows efficient biosynthesis of C3, C5, and C6 products starting from low cost and readily available C1 substrates and demonstrates the potential of the approach to convert C1 compounds into biologically produced higher-value products.
我们在这里通过结合从C1底物中产生乙酸的醋酸杆菌和谷氨酸棒状杆菌生长并从乙酸形成增值产品的能力,应用顺序微生物生物过程。在第一次发酵中,我们演示了在厌氧条件下用CO2加H2或甲醇生产高达400 mM的生物乙酸。在随后的培养中,我们使用C. glutamicum将乙酸衍生的生物乙酸转化为氨基酸L-谷氨酸(高达13.1 mM = 1.93 g L−1),或异源产物3-羟丙酸(高达40.8 mM = 3.68 g L−1)和甲戊酸(高达11.3 mM = 1.67 g L−1)。因此,本文提出的顺序发酵平台允许从低成本和现成的C1底物开始高效地生物合成C3, C5和C6产品,并展示了该方法将C1化合物转化为生物生产的高价值产品的潜力。