Salinity is one of the major anthropogenic as well as environmental stresses that reduce plant growth. Results show that even after being adapted up to 6% sodium chloride (NaCl) concentration, all selected isolates were able to solubilize phosphate, and produce phytohormones, siderophores and 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase enzyme. NT1 was found to exhibit the highest phosphate solubilization zones (25 mm), siderophore production (1000 µg ml⁻¹) as well as ACC deaminase production (50 µMmg⁻¹h⁻¹) potential under laboratory conditions. On the other hand, pot studies conducted on tomato plants under 2% NaCl stress proved that C4 and T15 were the best growth promoters. C4 showed 50% enhancement in root and shoot length as compared to NaCl added untreated plants as well as in absence of NaCl. C4 also enhanced salinity tolerance in plants with the lowest uptake of NaCl thereby reducing the salt stress on plants. C5 enhanced biomass production in tomato plants with increased uptake of the salts by plants, thereby reducing the salt concentration in the soil. The study thus shows that the selected isolates can be used for the plant growth promotion of plants under salinity stress.

Many rhizobacteria isolated from plant rhizosphere produce various phytohormones in the form of secondary metabolites, the most common of which is Indole-3-acetic acid (IAA). Here, we detail analytical protocols of IAA detection and quantification, in vitro and in situ, as recently applied to Klebsiella SGM 81, a rhizobacterium isolated from the rhizosphere of Dianthus caryophyllus (a commercially important flower across the globe). Specifically, we describe a detailed protocol for a colorimetric assay using the Salkowski reagent method, which can be used to screen for the presence of Indole compounds. To further detect and quantify IAA, a highly accurate analytical approach of LC-MS/MS is used. To detect the presence of IAA around the root system of Dianthus caryophyllus, in situ staining of plant roots is done using Salkowski reagent. Bio-protocol is an online peer-reviewed protocol journal. Its mission is to make life science research more efficient and reproducible by curating and hosting high quality, free access protocols.

The health of the plant and soil fertility is dependent on the plant–microbes interaction in the rhizosphere. Microbial life tends to endure various rhizosphere plant–microbe interactions. Phytohormones such as auxins, cytokinins, gibberellic acid, ethylene and abscisic acid are termed as the classical group of hormones. Out of the 70 rhizobacterial strains isolated from the Coleus rhizosphere, three different rhizobacterial strains Pseudomonas stutzeri MTP40, Stenotrophomonas maltophilia MTP42 and Pseudomonas putida MTP50 having plant growth-promoting attributes were isolated and characterized for its phytohormone-producing ability. The phytohormones such as indole 3-acetic acid (IAA), gibberellic acid and cytokinin (kinetin and 6-benzyladenosine) were affirmed in culture supernatant of the above isolates. IAA was detected in all the three isolates, where in highest production was found in S. maltophilia MTP42 (240 µg/mL) followed by P. stutzeri MTP40 (250 µg/mL) and P. putida MTP50 (233 µg/mL). Gibberellic acid production was found maximum in MTP40 (34 µg/mL), followed by MTP42 (31 µg/mL) and MTP50 (27 µg/mL). The cytokinin production from the isolates, namely, MTP40, MTP42 and MTP50 were 13, 11 and 7.5 µg/mL, respectively. The isolates showing the production of plant growth enhancing phytohormones can be commercialized as potent bioformulations.