“…VC synthesis usually relies on an initial chemical conversion of D-Glucose to D-Sorbitol followed by two independent fermentation steps using Gluconobacter oxydans and a mixed culture of Ketogulonigenium vulgare and Bacillus megaterium , respectively, to obtain 2-Keto-L-Gulonic acid [ 235 ], a VC precursor. This two-step fermentation method is highly efficient, but the hydrogenation of D-Glucose and the maintenance of balanced co-cultures still have economical and labor costs that can, in principle, be avoided [ 235 ], using for instance, a direct one-step fermentation process [ 235 , 236 ]. This can be achieved through the genetic integration of plant VC synthesis pathway components, such as the A. thaliana GALDH , in fungi [ 236 ], as well as the integration of genes involved in D-Sorbitol/L-Sorbose metabolism from different prokaryote sources into a single bacterial chassis [ 237 , 238 , 239 ].…”