Characterization of cultivable putative endophytic plant growth promoting bacteria associated with maize cultivars (Zea mays L.) and their inoculation effects in vitro

2012 ◽  
Vol 58 ◽  
pp. 21-28 ◽  
Author(s):  
Adriana Montañez ◽  
Andrea Rodríguez Blanco ◽  
Claudia Barlocco ◽  
Martin Beracochea ◽  
Margarita Sicardi
2020 ◽  
Vol 53 (2) ◽  
Author(s):  
Muhammad Mubeen ◽  
Asghari Bano ◽  
Barkat Ali ◽  
Zia Ul Islam ◽  
Ashfaq Ahmad ◽  
...  

Author(s):  
Lygia Vitória Galli Terasawa ◽  

Maize (Zea mays L.) culture has a great importance in several countries, especially in Brazil the third-largest world producer. The increase in maize production has been achieved with a high use of fungicide; however, in view of a more sustainable agriculture plant growth promoting bacteria have been explored aiming for the replacement of chemical fertilizers and biological control. In this study, we investigated the bacterial community isolated from maize roots in order to evaluate their capacity of growth promotion as well as of inhibition of fungal species associated with maize leaf diseases. All isolates evaluated were positive for at least one of the parameters evaluated-growth promotion, enzymatic production or bio control. The best results were observed for Enterobacter sp. LGMB221 and Bacillus sp. LGMB242 that showed the high potential for growth promotion, acting in the early stage of maize seedlings development. Bacillus sp. LGMB152 showed the best enzymatic results, indicating that it might play a role against pathogens, a premise supported by the antagonist activity observed. The next steps involve evaluations under field conditions to confirm if these isolates have biotechnological potential as inoculants for the maize crop. In addition, we suggest that Enterobacter strains LGMB221 and LGMB235 and Escherichia strain LGMB159 might represent new species, indicating the high diversity of bacteria in maize rhizosphere that remains to be determined.


Author(s):  
Lynda Kelvin Asogwa ◽  
Frank C. Ogbo

Aims: To isolate Plant Growth Promoting Bacillus strain from maize roots, to evaluate its biocontrol potentials and to characterize the isolate using16S rRNA sequencing. Place and Duration of Study: Department of Applied Microbiology and Brewing, Nnamdi Azikiwe University, Awka, between February 2019 and March 2020. Methodology: The isolation of Plant Growth Promoting Rhizobacteria (PGPR) from maize roots was done using Pikovskaya (PVK) agar. Quantitative determination of phosphate was carried out using PVK broth. Evaluations of other plant growth promoting properties were carried out such as IAA, etc. Fusarium and Enterobacter plant pathogens were isolated from diseased maize plants. The in vitro antagonism effects of the PGPR isolates against the pathogens were analyzed using the dual culture plate technique. The pot experiment was carried out in a completely randomized design. Plant characteristics such as plant height, shoot  and root weight, chlorophyll content, as well as disease assessment were recorded accordingly. The organisms were identified using phenotypic and molecular methods. Results: Seven PGPR bacteria were isolated from maize (Zea mays) roots using PVK agar. Aneurinibacillus migulanus gave the highest solubilization index of 4.21 while isolate IS48 gave the lowest solubilization index of 1.47. A. migulanus produced IAA, ammonia and cellulase enzyme but no hydrogen cyanide. The organism showed antagonism activity against the two tested phytopathogens. In the pot experiment, A. migulanus treated plants showed a statistically insignificant difference in maize plant height at P=0.05 but gave significant increases in shoot and root wet weights. The organism offered 83.33% and 71.43% protection against Enterobacter and Fusarium pathogens respectively in the pot experiment. Conclusion: A. migulanus solubilized phosphate in addition to other plant growth promoting  properties. It showed biocontrol potentials both in vitro and in vivo and thus can be used as substitute for synthetic agrochemicals.


Sign in / Sign up

Export Citation Format

Share Document