Jeong E-L, Broad S J, Moody R G, Phillips-Jones M K
Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, United Kingdom.
Department of Molecular Biology & Biotechnology, University of Sheffield, Sheffield, S10 2TN, United Kingdom.
Int J Hydrogen Energy. 2020 Oct 16;45(51):26840-26854. doi: 10.1016/j.ijhydene.2020.07.108.
Expression of encoding a fasciclin I domain protein important for adherence in the hydrogen-producing bacterium was investigated under a range of conditions to gain insights into optimization of adherence for immobilization strategies suitable for H production. The promoter was linked to a reporter and expressed in wild type and in PRRB and PRRA mutant strains of the Prr regulatory pathway. Expression was significantly negatively regulated by Prr under all conditions of aerobiosis tested including anaerobic conditions (required for H production), and aerobically regardless of growth phase, growth medium complexity or composition, carbon source, heat and cold shock and dark/light conditions. Negative regulation by Prr was reflected in cellular levels of translated Fdp protein. Since Prr is required directly for nitrogenase expression, we propose optimization of Fdp-based adherence in for immobilized biohydrogen production by inactivation of the PrrA binding site(s) upstream of .
为深入了解适用于产氢的固定化策略中附着的优化方法,在一系列条件下研究了编码对产氢细菌附着至关重要的成束蛋白I结构域蛋白的表达情况。将该启动子与一个报告基因相连,并在野生型以及Prr调节途径的PRRB和PRRA突变菌株中表达。在所有测试的需氧条件下,包括产氢所需的厌氧条件,以及无论生长阶段、生长培养基复杂性或组成、碳源、热和冷休克以及黑暗/光照条件的有氧条件下,Prr均对表达产生显著的负调控作用。Prr的负调控作用体现在翻译后的Fdp蛋白的细胞水平上。由于Prr是固氮酶表达直接所需的,我们建议通过使该基因上游的PrrA结合位点失活来优化基于Fdp的附着,以用于固定化生物制氢。