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Plant growth promoting rhizobacteria (PGPR) are known to influence plant growth by various direct or indirect mechanisms. In search of efficient PGPR strains with multiple activities, a total of 72 bacterial isolates belonging to
Azotobacter, fluorescent
Pseudomonas,
Mesorhizobium and
Bacillus were isolated from different rhizospheric soil and plant root nodules in the vicinity of Aligarh. These test isolates were biochemically characterized. These isolates were screened
in vitro for their plant growth promoting traits like production of indoleacetic acid (IAA), ammonia (NH
3), hydrogen cyanide (HCN), siderophore, phosphate solubilization and antifungal activity. More than 80% of the isolates of
Azotobacter, fluorescent
Pseudomonas and
Mesorhizobium ciceri produced IAA, whereas only 20% of
Bacillus isolates was IAA producer. Solubilization of phosphate was commonly detected in the isolates of
Bacillus (80%) followed by
Azotobacter (74.47%),
Pseudomonas (55.56%) and
Mesorhizobium (16.67%). All test isolates could produce ammonia but none of the isolates hydrolyzed chitin. Siderophore production and antifungal activity of these isolates except
Mesorhizobium were exhibited by 10–12.77% isolates. HCN production was more common trait of
Pseudomonas (88.89%) and
Bacillus (50%). On the basis of multiple plant growth promoting activities, eleven bacterial isolates (seven
Azotobacter, three
Pseudomonas and one
Bacillus) were evaluated for their quantitative IAA production, and broad-spectrum (active against ⩾ three test fungi) antifungal activity. Almost at all concentration of tryptophan (50–500
μg/ml), IAA production was highest in the
Pseudomonas followed by
Azotobacter and
Bacillus isolates
. Azotobacter isolates (AZT
3, AZT
13, AZT
23),
Pseudomonas (Ps
5) and
Bacillus (B
1) showed broad-spectrum antifungal activity on Muller-Hinton medium against
Aspergillus, one or more species of
Fusarium and
Rhizoctonia bataticola. Further evaluation of the isolates exhibiting multiple plant growth promoting (PGP) traits on soil–plant system is needed to uncover their efficacy as effective PGPR.