Department of Genetics, Osmania University, Hyderabad, India.
Department of Biotechnology, Vignan's Foundation for Science, Technology and Research, Guntur, India.
Physiol Plant. 2021 Dec;173(4):1351-1368. doi: 10.1111/ppl.13369. Epub 2021 Mar 5.
Genes encoding bacterial cold shock proteins A (CspA, 213 bp) and B (CspB, 216 bp) were isolated from Escherichia coli strain K12, which showed 100% homology with gene sequences isolated from other bacterial species. In silico domain, analysis showed eukaryotic conserved cold shock domain (CSD) and ribonuclease-binding domain (RBD) indicating that they bind to RNA and are involved in temperature stress tolerance. Overexpression of these two genes in E. coli resulted in higher growth in presence of 200 mM NaCl and 300 mM mannitol. Western blot confirmed the translational products of the two genes. Seedlings of indica rice were transformed with Agrobacterium tumefaciens containing pCAMBIA1301 CspA and CspB genes. Transgene integration was confirmed by β-glucuronidase (GUS) histochemical assay, polymerase chain reaction (PCR) amplification, and gene copy number by Southern blotting. Chlorophyll, proline, Na , and K contents were higher in transgenics exposed to 150 mM NaCl and drought (imposed by withholding water) stresses during floral initiation stage. Catalase (CAT), superoxide dismutase (SOD), and guaiacol peroxidase (GPX) activities increased, while malondialdehyde (MDA) content was low in transgenics. Transgenics displayed increased root, shoot, and panicle lengths, root dry mass, and a distinct stay-green (SGR) phenotype. Higher transcript levels of CspA, CspB, SGR, chlorophyllase, isopentenyl adenine transferase 1 (IPT1), 9-cis-epoxycarotenoid dioxygenase (NCED), SOD, and sirtuin 1 (SIRT1) genes were observed in transgenics compared to wild type plants (WT) under multiple stresses. Present work indicates that bacterial chaperone proteins are capable of imparting SGR phenotype, salt and drought stress tolerance alongside grain improvement.
从大肠杆菌菌株 K12 中分离出编码细菌冷休克蛋白 A(CspA,213bp)和 B(CspB,216bp)的基因,它们与从其他细菌物种中分离出的基因序列具有 100%的同源性。计算机域分析显示真核生物保守冷休克域(CSD)和核糖核酸酶结合域(RBD),表明它们与 RNA 结合,并参与温度应激耐受。这两个基因在大肠杆菌中的过表达导致在存在 200mM NaCl 和 300mM 甘露醇的情况下生长更高。Western blot 证实了这两个基因的翻译产物。用含有 pCAMBIA1301 CspA 和 CspB 基因的根癌农杆菌转化籼稻幼苗。通过β-葡萄糖醛酸酶(GUS)组织化学分析、聚合酶链反应(PCR)扩增和Southern 印迹法基因拷贝数证实了转基因的整合。在花起始阶段暴露于 150mM NaCl 和干旱(通过停水施加)胁迫下,转基因中的叶绿素、脯氨酸、Na+和 K+含量较高。在转基因中,过氧化氢酶(CAT)、超氧化物歧化酶(SOD)和愈创木酚过氧化物酶(GPX)的活性增加,而丙二醛(MDA)含量较低。转基因表现出增加的根、茎和穗长、根干质量和明显的持绿(SGR)表型。与野生型植物(WT)相比,在多种胁迫下,转基因中 CspA、CspB、SGR、叶绿素酶、异戊烯基腺嘌呤转移酶 1(IPT1)、9-顺式-环氧类胡萝卜素双加氧酶(NCED)、SOD 和 SIRT1 基因的转录水平更高。目前的工作表明,细菌伴侣蛋白能够赋予 SGR 表型、耐盐和耐旱性以及提高谷物产量。