The global agriculture sector is under tremendous pressure to meet the growing food demand accelerated by increasing population. This is worsened with the rising phenomenon of soil salinization of arable land attributable to global warming. Therefore, there is a need to develop sustainable agricultural methods to enhance the salinity tolerance of crops. The date palm (Phoenix dactylifera L.) is the most important crop, with over 250 varieties, cultivated in the arid regions of the Middle East and North Africa. In Oman, there are about 250 varieties of date palm cultivated occupying 50% of the total agricultural land and comprising about 80% of the entire fruit trees grown in the country. However, various factors such as high evaporation, lack of precipitation, and the indiscriminate use of underground water have led to an increase in soil salinization, which in turn has hampered the date production. Therefore, the aim of this thesis is to study the potential use of Plant Growth Promoting Rhizobacteria (PGPR) and silicon in enhancing the salinity tolerance of date palm. We identified an Achromobacter xylosoxidans SQU1 (SQU-1) strain and a microbial volatile organic compounds (mVOC) producing Enterobacter cloacae SQU-2 (SQU-2) strain which were able to enhance the growth of Arabidopsis seedlings under salinity stress in vitro. The genomes of these strains were further sequenced to identify the potential genes that may be involved in plant growth promotion. Analysis of the genome sequence of SQU-1 resulted in the identification of the 1-aminocyclopropane-1-carboxylate deaminase gene, which encodes for the enzyme that degrades 1-aminocyclopropane-1-carboxylate, the main precursor for the vii biosynthesis of stress hormone ethylene. Also, other plant growth-promoting gene clusters including those that code for enzymes producing siderophore and antibiotics. Whereas from the genome of SQU-2 the gene clusters relating to the synthesis of growthpromoting mVOC 2,3-butanediol and acetoin along with the other growth-promoting genes were identified. Further, the use of 5 mM Na2SiO3 as a soluble form of silicon was able to enhance salt tolerance mechanism of the date palm seedlings. Therefore, to gain further insight into how silicon can confer salinity tolerance to the date palm seedlings a global untagged metabolite profiling using the hydrophilic interaction liquid chromatography (HILIC) and reverse-phase liquid chromatography (RPLC) was performed. The analysis resulted in the identification of 1101 significantly (p ≤ 0.05) accumulated metabolites in the leaf and root tissues in response to salinity and silicon treatment of which 836 and 839 metabolites were identified in the leaf and root tissues, respectively. Among them 345 metabolites were shared between both the tissue types under the different conditions. Further analyses of the different accumulated metabolites suggested that silicon may enhance antioxidative and detoxification of various toxins including, cytotoxic metabolite methylglyoxal (MG) via glyoxalase I, II and III system, the detoxification and redox balance through the gamma-glutamyl cycle and enhanced hydrogen cyanide detoxification. From this study, three potential gene families were further investigated for their roles in salinity tolerance mechanisms in date palm, including the six glutathione peroxidase (PdGPX) genes, five Glyoxalase I (PdGLX1) genes and four Glyoxalase III (PdDJ-1) genes. Their expression profile quantified by real-time PCR (qPCR) revealed that the genes are expressed in a tissue-specific manner in response to various environmental cues. Further, heterologous overexpression of the different PdGPX, PdGLX1, and PdDJ-1 genes in BL21 (DE3) showed enhanced growth under salinity (250 mM NaCl), oxidative (5 mM H2O2) and exogenous MG (0.5 mM MG) viii stress conditions. In addition, the genes were able to complement the loss of function of the H2O2- sensitive GPX3D, MG hypersensitive GLO1 and oxidative sensitive Hsp31D knock out yeast mutants respectively. In addition, the heterologous overexpression of a PdDJ-1C in Arabidopsis resulted in the production of non-viable albino phenotype, thereby suggesting that the PdDJ-1C plays an important role in chloroplast development.