Adhikary Hemanta, Sanghavi Paulomi B, Macwan Silviya R, Archana Gattupalli, Naresh Kumar G
Department of Biochemistry, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, Gujarat, India.
Department of Microbiology and Biotechnology Centre, Faculty of Science, The Maharaja Sayajirao University of Baroda, Vadodara, Gujarat, India.
PLoS One. 2014 Sep 26;9(9):e107554. doi: 10.1371/journal.pone.0107554. eCollection 2014.
Citric acid is a strong acid with good cation chelating ability and can be very efficient in solubilizing mineral phosphates. Only a few phosphate solubilizing bacteria and fungi are known to secrete citric acids. In this work, we incorporated artificial citrate operon containing NADH insensitive citrate synthase (gltA1) and citrate transporter (citC) genes into the genome of six-plant growth promoting P. fluorescens strains viz., PfO-1, Pf5, CHAO1, P109, ATCC13525 and Fp315 using MiniTn7 transposon gene delivery system. Comprehensive biochemical characterization of the genomic integrants and their comparison with plasmid transformants of the same operon in M9 minimal medium reveals the highest amount of ∼7.6±0.41 mM citric and 29.95±2.8 mM gluconic acid secretion along with ∼43.2±3.24 mM intracellular citrate without affecting the growth of these P. fluorescens strains. All genomic integrants showed enhanced citric and gluconic acid secretion on Tris-Cl rock phosphate (TRP) buffered medium, which was sufficient to release 200-1000 µM Pi in TRP medium. This study demonstrates that MPS ability could be achieved in natural fluorescent pseudomonads by incorporation of artificial citrate operon not only as plasmid but also by genomic integration.
柠檬酸是一种具有良好阳离子螯合能力的强酸,在溶解矿物磷酸盐方面非常有效。已知只有少数解磷细菌和真菌能分泌柠檬酸。在这项研究中,我们使用MiniTn7转座子基因递送系统,将包含对NADH不敏感的柠檬酸合酶(gltA1)和柠檬酸转运蛋白(citC)基因的人工柠檬酸操纵子整合到六种促进植物生长的荧光假单胞菌菌株的基因组中,即PfO-1、Pf5、CHAO1、P109、ATCC13525和Fp315。在M9基本培养基中对基因组整合体进行全面的生化特性分析,并将其与相同操纵子的质粒转化体进行比较,结果显示,这些荧光假单胞菌菌株分泌的柠檬酸和葡萄糖酸量最高,分别约为7.6±0.41 mM和29.95±2.8 mM,细胞内柠檬酸含量约为43.2±3.24 mM,且不影响这些菌株的生长。所有基因组整合体在Tris-Cl磷矿石(TRP)缓冲培养基上的柠檬酸和葡萄糖酸分泌均有所增强,这足以在TRP培养基中释放200-1000 µM的磷。这项研究表明,通过整合人工柠檬酸操纵子,不仅可以以质粒形式,还可以通过基因组整合,在天然荧光假单胞菌中实现解磷能力。