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Contribution of cellulose synthesis, formation of fibrils and their entanglement to the self‐flocculation of Zymomonas mobilis

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Due to the unique Entner‐Doudoroff pathway, Zymomonas mobilis has been acknowledged as a potential host to be engineered for biorefinery to produce biofuels and biobased chemicals. The self‐flocculation of Z.… Click to show full abstract

Due to the unique Entner‐Doudoroff pathway, Zymomonas mobilis has been acknowledged as a potential host to be engineered for biorefinery to produce biofuels and biobased chemicals. The self‐flocculation of Z. mobilis can make the bacterial cells self‐immobilized within bioreactors for high density to improve product productivities, and in the meantime enhance their tolerance to stresses, particularly product inhibition and the toxicity of byproducts released during the pretreatment of lignocellulosic biomass. In this work, we explored mechanism underlying such a phenotype with the self‐flocculating strain ZM401 developed from the regular non‐flocculating strain ZM4. Cellulase de‐flocculation and the restoration of the self‐flocculating phenotype for the de‐flocculated bacterial cells subjected to culture confirmed the essential role of cellulose biosynthesis in the self‐flocculation of ZM401. Furthermore, the deactivation of both Type I and Type IV restriction‐modification systems was performed for ZM4 and ZM401 to improve their transformation efficiencies. Comparative genome analysis detected the deletion of a thymine from ZMO1082 in ZM401, leading to a frame‐shift mutation for the putative gene to be integrated into the neighboring downstream gene ZMO1083 encoding the catalytic subunit A of cellulose synthase, and consequently created a new gene to encode a larger transmembrane protein BcsA_401 for more efficient synthesis of cellulose as well as the development of cellulose fibrils and their entanglement for the self‐flocculation of the mutant. These speculations were confirmed by the morphological observation of the bacterial cells under scanning electron microscopy, the impact of the gene deletion on the self‐flocculation of ZM401, and the restoration of the self‐flocculating phenotype of ZM401 ΔbcsA by the gene complementation. The progress will lay a foundation not only for fundamental research in deciphering molecular mechanisms underlying the self‐flocculation of Z. mobilis and stress tolerance associated with the morphological change but also for technological innovations in engineering non‐flocculating Z. mobilis and other bacterial species with the self‐flocculating phenotype.

Keywords: self flocculation; mobilis; zm401; gene; flocculation

Journal Title: Biotechnology and Bioengineering
Year Published: 2018

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