Salinity is a major environmental stress that limits crop production worldwide. In this study, we characterized plant growth-promoting rhizobacteria (PGPR) containing 1-aminocyclopropane-1-carboxylate (ACC) deaminase and examined their effect on salinity stress tolerance in okra through the induction of ROS-scavenging enzyme activity. PGPR inoculated okra plants exhibited higher germination percentage, growth parameters, and chlorophyll content than control plants. Increased antioxidant enzyme activities (SOD, APX, and CAT) and upregulation of ROS pathway genes (CAT, APX, GR, and DHAR) were observed in PGPR inoculated okra plants under salinity stress. With some exceptions, inoculation with Enterobacter sp. UPMR18 had a significant influence on all tested parameters under salt stress, as compared to other treatments. Thus, the ACC deaminase-containing PGPR isolate Enterobacter sp. UPMR18 could be an effective bioresource for enhancing salt tolerance and growth of okra plants under salinity stress.

Biofertilizer is a relatively safer, environmentally friendly and cost-effective approach as an alternative to reduce chemical fertilizer usage. The selection of bacterial strains with multiple beneficial characteristics are important to maximize the effectiveness on the host plant. Due to aforementioned interest, several Plant Growth-Promoting Rhizobacterial (PGPR) and rhizobial strains were isolated from rice and legume roots, respectively, at four locations in Malaysia namely Universiti Putra Malaysia (UPM), Serdang, Selangor; Besut, Terengganu; Tunjung, Kelantan and Sik, Kedah. Bacterial isolations were undertaken to select the best isolates which exhibit multiple beneficial effects to the rice plant and a total of 205 bacterial strains were isolated and categorized as follows; 94 rhizospheric and 107 endophytic bacteria from rice roots, one rhizobial strain from soybean and three from Mimosa pudica. These isolates were screened for their abilities to fix N 2 and solubilize phosphate; 52 were positive for both tests. The selected isolates were then tested for IAA production and other biochemical tests such as potassium solubilization, hydrolyzing enzymes (cellulase and pectinase) and iron siderophore productions. Four isolates, namely UPMB19 (rhizospheric PGPR from Tunjung, Kelantan), UPMB20 (endophytic PGPR from Besut, Terengganu), UPMR30 (rhizobia from soybean) and UPMR31 (rhizobia from Mimosa) were selected for subsequent plant inoculation tests with UPMB10, a PGPR isolated from oil palm root, as the reference strain. Based on 16S rDNA gene sequencing, these bacterial strains were identified under several genera: Lysinibacillus, Alcaligenes, Bradyrhizobium, Rhizobium and Bacillus, respectively. Results of plant inoculation test indicated that UPMB19 significantly enhanced the seedling height at the early growth stage (7 days after transplanting, DAT) which could be attributed to the higher N 2 fixation rate of this strain as compared to the other strains, except UPMB20. UPMB10 and UPMR31 also showed significant effects with increased seedling height and Total Dry Weight (TDW) at the later stage (14 DAT) possibly due to the higher bacterial population and IAA produced as observed in the residual nutrient solution without addition of fertilizer-N. This study has successfully demonstrated the effectiveness of locally isolated PGPR and rhizobial strains with multiple beneficial characteristics on early growth and vigor of rice seedlings under controlled condition. The result proved to be a vital information in the development of a liquid biofertilizer for rice; thus further studies will be done to evaluate the effectiveness of these isolates under glasshouse and field conditions on growth, tillering and yield of rice.

The study was undertaken to characterize plant growth promoting rhizobacteria (PGPR) for growth enhancement and stress tolerant traits and their efficacy on early establishment of rice seedling. In vitro growth promoting traits revealed that out of 30 PGPR isolates, 18 fixed nitrogen, 17 solubilized tri-calcium phosphate, 29 and 17 produced IAA with or without addition of L-tryptophane. In case of stress tolerant activities, PGPR isolates tolerated pH ranging from 5 to 10, Nacl from 1 to 6% and polyethylene glycol (PEG) from 10 to 40%, respectively. They showed antagonistic activity against Pyricularia oryzae with PIRG values ranging from 7−68%. After two-stage of screening, isolates UPMR7 and UPMR17 were identified based on 16s rRNA gene sequences and matched to the genus Bacillus and Citrobacter with 97−98% similarity. UPMR 7 and UPMR 17 were further evaluated on early growth promotion of rice variety MR219. Results revealed that PGPR inoculation had significant effects on plant growth compared to non-inoculated plants. Thus, it could be suggested that the isolates UPMR7 and UPMR17 have the potential to be used as biofertilizer and bioenhancer in sustainable rice cultivation.

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