Schultenkämper Kerstin, Gütle Desirée D, López Marina Gil, Keller Laura B, Zhang Lin, Einsle Oliver, Jacquot Jean-Pierre, Wendisch Volker F
Genetics of Prokaryotes, Faculty of Biology & CeBiTec, Bielefeld University, Bielefeld, Germany.
INRAE, IAM, Université de Lorraine, Nancy, France.
Front Microbiol. 2021 Apr 30;12:669220. doi: 10.3389/fmicb.2021.669220. eCollection 2021.
The Gram-positive shows plasmid-dependent methylotrophy. This facultative ribulose monophosphate (RuMP) cycle methylotroph possesses two fructose bisphosphate aldolases (FBA) with distinct kinetic properties. The chromosomally encoded FBA is the major glycolytic aldolase. The gene for the major gluconeogenic aldolase FBA is found on the natural plasmid pBM19 and is induced during methylotrophic growth. The crystal structures of both enzymes were solved at 2.2 Å and 2.0 Å, respectively, and they suggested amino acid residue 51 to be crucial for binding fructose-1,6-bisphosphate (FBP) as substrate and amino acid residue 140 for active site zinc atom coordination. As FBA and FBA differed at these positions, site-directed mutagenesis (SDM) was performed to exchange one or both amino acid residues of the respective proteins. The aldol cleavage reaction was negatively affected by the amino acid exchanges that led to a complete loss of glycolytic activity of FBA. However, both FBA and FBA maintained gluconeogenic aldol condensation activity, and the amino acid exchanges improved the catalytic efficiency of the major glycolytic aldolase FBA in gluconeogenic direction at least 3-fold. These results confirmed the importance of the structural differences between FBA and FBA concerning their distinct enzymatic properties. In order to investigate the physiological roles of both aldolases, the expression of their genes was repressed individually by CRISPR interference (CRISPRi). The RNA levels were reduced by CRISPRi, but concomitantly the RNA levels were increased. Vice versa, a similar compensatory increase of the RNA levels was observed when was repressed by CRISPRi. In addition, targeting decreased RNA levels since both genes are cotranscribed in a bicistronic operon. However, reduced RNA levels were not compensated for by increased RNA levels of the chromosomal transketolase gene .
革兰氏阳性菌表现出质粒依赖性甲基营养。这种兼性的磷酸戊糖(RuMP)循环甲基营养菌拥有两种具有不同动力学特性的果糖二磷酸醛缩酶(FBA)。染色体编码的FBA是主要的糖酵解醛缩酶。主要的糖异生醛缩酶FBA的基因位于天然质粒pBM19上,并在甲基营养生长过程中被诱导。两种酶的晶体结构分别在2.2 Å和2.0 Å下解析,结果表明氨基酸残基51对于结合果糖-1,6-二磷酸(FBP)作为底物至关重要,而氨基酸残基140对于活性位点锌原子的配位至关重要。由于FBA和FBA在这些位置存在差异,因此进行了定点诱变(SDM)以交换各自蛋白质的一个或两个氨基酸残基。氨基酸交换对醛醇裂解反应产生负面影响,导致FBA的糖酵解活性完全丧失。然而,FBA和FBA都保持了糖异生醛醇缩合活性,并且氨基酸交换使主要的糖酵解醛缩酶FBA在糖异生方向上的催化效率至少提高了3倍。这些结果证实了FBA和FBA之间结构差异对于其不同酶学特性的重要性。为了研究两种醛缩酶的生理作用,通过CRISPR干扰(CRISPRi)分别抑制了它们的基因表达。CRISPRi降低了RNA水平,但同时RNA水平却升高了。反之,当通过CRISPRi抑制时,观察到RNA水平有类似的补偿性增加。此外,靶向降低了RNA水平,因为这两个基因在双顺反子操纵子中共同转录。然而,RNA水平的降低并未被染色体转酮醇酶基因RNA水平的升高所补偿。