“…Sample growth 2.1.1. Microbial strains and chemicals We used the same microbial strain, consumables and pre-culturing method as described in an earlier work [9]. These were, for all experiments, the non-motile [15] Komagataeibacter sucrofermentans (DSM-15973, German Collection of Microorganisms and Cell Cultures, Braunschweig, Germany) and agar, yeast extract, disodium hydrogen phosphate, citric acid, ethanol absolut (VWR, Darmstadt, Germany), D-(+)-Sucrose, chloramphenicol, peptone from meat (Carl Roth, Karlsruhe, Germany) and sodium hydroxide (Acros Organics, Geel, Belgium).…”