It appears you don't have support to open PDFs in this web browser. To view this file, Open with your PDF reader
Abstract
Cell division can perturb the metabolic performance of industrial microbes. The C period of cell division starts from the initiation to the termination of DNA replication, whereas the D period is the bacterial division process. Here, we first shorten the C and D periods of E. coli by controlling the expression of the ribonucleotide reductase NrdAB and division proteins FtsZA through blue light and near-infrared light activation, respectively. It increases the specific surface area to 3.7 μm−1 and acetoin titer to 67.2 g·L−1. Next, we prolong the C and D periods of E. coli by regulating the expression of the ribonucleotide reductase NrdA and division protein inhibitor SulA through blue light activation-repression and near-infrared (NIR) light activation, respectively. It improves the cell volume to 52.6 μm3 and poly(lactate-co-3-hydroxybutyrate) titer to 14.31 g·L−1. Thus, the optogenetic-based cell division regulation strategy can improve the efficiency of microbial cell factories.
Manipulation of genes controlling microbial shapes can affect bio-production. Here, the authors employ an optogenetic method to realize dynamic morphological engineering of E. coli replication and division and show the increased production of acetoin and poly(lactate-co-3-hydroxybutyrate).
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details


1 Jiangnan University, State Key Laboratory of Food Science and Technology, Wuxi, China (GRID:grid.258151.a) (ISNI:0000 0001 0708 1323); Jiangnan University, Key Laboratory of Industrial Biotechnology, Ministry of Education, Wuxi, China (GRID:grid.258151.a) (ISNI:0000 0001 0708 1323)
2 Central South University of Forestry and Technology, Hunan Provincial Key Laboratory for Forestry Biotechnology, Changsha, China (GRID:grid.440660.0) (ISNI:0000 0004 1761 0083)
3 Jiangnan University, State Key Laboratory of Food Science and Technology, Wuxi, China (GRID:grid.258151.a) (ISNI:0000 0001 0708 1323); Jiangnan University, Key Laboratory of Industrial Biotechnology, Ministry of Education, Wuxi, China (GRID:grid.258151.a) (ISNI:0000 0001 0708 1323); Jiangnan University, National Engineering Laboratory for Cereal Fermentation Technology, Wuxi, China (GRID:grid.258151.a) (ISNI:0000 0001 0708 1323)