Isolation and Biochemical Identification of N2 Fixing Bacteria (Azospirillium Sp.) from Saurashtra Region

Sarvangi Rabara1, Nutan Prakash Vishwakarma2*and Shivani Patel3

1Department of Microbiology, Atmiya University

2Department of Biotechnology, Atmiya University.

3Department of Biotechnology and Microbiology, Atmiya University

Corresponding Author E-mail:nutan.vishwakarma@atmiyauni.ac.in

DOI : http://dx.doi.org/10.12944/CARJ.11.1.24

Article Publishing History

Received: 30 Jan 2023
Accepted: 25 Apr 2023
Published Online: 03 May 2023

Review Details

Plagiarism Check: Yes
Reviewed by: Dr. S. Bala Murugan
Second Review by: Dr. Hemant Kumar
Final Approval by: Dr. Surendra Singh Bargali

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Abstract:

Azospirillium species are widely used as Biofertilizer to increase crop yield and are free-living nitrogen-fixing bacteria, one of the best-studied plant growth-promoting Rhizobacteria. It is commonly found along with the roots of many different plant species. The present study included the isolation of Azospirillium species from roots and soils in Rhizospheric regions. 50 isolates were isolated from fields in different districts of Saurashtra region in Gujarat against NFB Medium. Significant isolates were isolated from the root surface and root internal tissues. These 50 were morphologically identified and biochemically characterized isolates included the techniques documented in Bergey's Textbook of Identified Bacteria 9th edition (TSI- Triple Sugar Iron, GPB- Glucose Phosphate Broth, MR- Methyl Red VP- Voges Proskauer, TRP-Tryptophan, PNB- Peptone Nitrate Broth, Carbohydrate) out of which fifteen isolates were biochemically positive and were also capable of producing IAA (Indole Acetic Acid), and were also capable of producing IAA.

Keywords:

Bio fertilizer; Carbohydrate; GPB; IAA; NFB Medium; Rhizobacteria; Rhizospheric

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Rabara S, Vishwakarma N. P, Patel S. Isolation and Biochemical Identification of N2 Fixing Bacteria (Azospirillium Sp.) from Saurashtra Region. Curr Agri Res 2023; 11(1). doi : http://dx.doi.org/10.12944/CARJ.11.1.24

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Rabara S, Vishwakarma N. P, Patel S. Isolation and Biochemical Identification of N2 Fixing Bacteria (Azospirillium Sp.) from Saurashtra Region. Curr Agri Res 2023; 11(1). Available from: https://bit.ly/3p3v6fq


Introduction

Today’s global scenario presents many constraints to agricultural production, leading to a decline in soil and soil fertility as well as a decline in agricultural output in general. Things are even worse for resource-poor farmers, who cannot afford to use high doses of organic fertilizers for crop production 1. By 2020, 28.8 million tons of nutrients are needed to produce million tons (approximately 321 million) of grain. However, available nutrients were 21.6 million tons – a wide gap of 7.2 million tons between nutrient supply and nutrient removal. 2 In addition to reducing urea-N and preventing soil depletion, biological nitrogen fixation (BNF) technology also considerably lowers environmental pollution.3 Since they are beneficial to the environment and economical for farmers, organic fertilisers are seen to be a key component in productivity, soil sustainability, and environmental protection 4. Farmers may gain financially from using this organic fertiliser, which also assures continued food production. The worldwide green revolution will begin with the application of chemical-free fertilisers or microbial inoculation.5

Bio-fertilizers are mainly live microbial products including bacteria, algae and fungi, singly or in combination with the effect of improving nutrients available in the soil for plants. Essential nutrients change from unusable to usable form with the assistant of microbial activities; activities also include phosphate solubilization, nitrogen fixation, soil biodegradation and plant growth hormone secretion. Bio-fertilizers are ecological, high-yielding, easier for farmers to use and more efficient.2

Azospirillium species

The genera Azotobacter and Azospirillium increase the yield of cereals and legumes under field conditions. 4 Azospirillium is solitary of the earliest identified/discovered and best-characterized plants that promote rhizobacteria covering tropical and temperate regions commonly applied to grass, rice, wheat, sugarcane and many other crops. 6. It grows profusely at pH-7 and can form spores in acidic soils at pH 4.8. Azosprilllium is a motile, non-fermenting, vibrioid, gram-negative nitrogen-fixing rhizome. It is an encapsulated microcapsule; Sheath are composed of a network of inverse polysaccharides ensuring stress tolerance and increased shelf life. Azospirillium is an α subgenus of proteobacteria with the original name Spirillum lipoferumisolated by Beijerinck from the Netherlands Laterly, by Schroder in 1932 from the soil of Germany and Austria7. The organism showed increased nitrogen content in the N2-free medium. Azospirillium can grow aerobically and anaerobically in different geographical climates. It uses organic acids on sugars as carbon sources, ammonium or nitrates as nitrogen sources, and it can fix nitrogen under microscopic and free living conditions8. A number of processes, including as the production and release of amino acids, IAA (indole acetic acid), Cytokines, Gibberellins, and other polyamines, as well as root development and the subsequent increase in water and nutrient intake, all work to promote Azospirillium. A huge genus, Azospirillium, has around 113 plant species from 35 different plant families. 9-10 Analyzed the results of multiple field trials with different non-legume crops, representing more than 20 years worldwide in a variety of weather and soil conditions, examining that 30% yield increase can reach 70% response time with Azospirillum inoculation. 11 reported that Azospirillum sp. inoculated on upland crops showed yield responses in winter cereals (14.0%), summer cereals (9.5%), and also in legumes (6.6%). 12 reported Azospirillum spp. isolated from Himalaya valley and other places from Lake Baiyang. The species isolated in 2019 were A.palustre 13, A. griseum 14, A. Ramasamy 15, A.Agricola 16, A.soli 17, Nitrospirillum & Niveispirillum 18, A.Himalayense 19, A.fermentation 20, A.Humicireducens 21, A.formosense 22, A.thiophilum 23, A.palatum 24, A.picis 25, A .rugosum 24, A.canadense & A.zeae 26, A.melinis 27, A.oryzae 28, A.doeberinerae 29, A.largimobile 30, A.irakense 31, A. .halopraeferens 32, A.amazonense 33, A.lipoferum & A.brasilense 34.

Root attachment to surface and site of root colonization

Sites suitable for colony colonisation have been shown to be where Azospirillum colonisation occurs on the surface of roots. In the most studied plant species, the bacteria form aggregation colonies that are supported by enormous fibrous material around the tips of elongated hairs and roots. Two distinct phases of Azospirillum’s attachment to wheat have been examined by 35. Bacterial proteins rule the quick and weak adsorption phase. The second phase is more prolonged, active, and irreversible; it could be based on the extracellular surface polysaccharides of bacteria.

The country becomes more self-sufficient in food production thanks to the use of chemical fertilisers, but this practise damages the environment, has negative effects on human health, contaminates groundwater, and promotes soil acidification owing to a decline in organic matter. Owing to inadequate plant absorption of these chemical fertilisers, they enter water bodies through rains, create eutrophication there, and have an impact on aquatic life. Finding management practises that can impact plant development, a general improvement in root growth, significant bio-control activities, and numerous mechanisms of the plant-microorganism interplay will be a future issue.

Materials and Methods

In the present investigation, the Azospirillium isolates mentioned in Table 1 were derived from the rhizomes of different non-legumes collected from different districts of Saurashtra region.

Sample collection

The Isolates were collected at a depth of 5-6 cm from the Rhizome Zone of the Plants (Maize, Cotton, Jowar, Sugarcane, Bajra, Wheat, Groundnut etc.) stored at 4 ℃. Species were isolated from roots and soil by serial dilution.36

Root isolation

Roots, washed thoroughly with water, cut into small pieces and shaken in a shaker for 30 min in sterile distilled water; 0.1 ml of water was inoculated into NFB semi-solid medium and incubated for 5-7 days at 30-35 °C to form a white film 37,38.

Soil Isolation

1 g soil was diluted in order to 10-6 with sterile distilled water. 1 ml of 10-4 to 10-6 diluent was incubated in tubes containing semi-solid NFB medium (Nitrogen-Free Bromothymol) and incubated for 5-7 days at 30-35°C to form films. These films have demonstrated positive results for the development of Azospirillium. Colonies were spread on Petri dishes containing solid NFB medium (Bromothymol without Nitrogen) and incubated at 30-35 °C for 72 h to isolate single colonies39.

Media Formulation

NFB medium contains 5 g malic acid, 4.0 g sodium chloride, 0.5 g potassium phosphate, 0.05 g ferric sulfate, 0.01 g manganese sulfate, 0.10 g magnesium sulfate, 0.02 g sodium chloride, 0.01 g calcium chloride, 0.002 g sodium molybdate dihydrate, 1000 ml water distillation, 2.0 ml bromothymol blue (BTB) – (0.5% alcohol solution) Final pH 6.6 to 6.8, 1.75 g of semi-solid medium and 15 g of solid medium 40,41.

Morphology and Classification

The juvenile inoculum from the semi-solid medium was applied on a clean slide, thermostated, then flooded with iodine for 1 minute, decolored with ethanol 95% in a matter of seconds, gently rinsed with tap water, and cleaned with Safranin stains. For viewing with an oil immersion lens, slides were air-dried 42. Gram-negative, rod-, spiral-, spiral-, and filamentous bacteria were seen under a microscope. The physical characteristics of the Azospirillium isolates are listed in Table 2.

Biochemical Characteristics

According to Bergey’s Guide to Determining Bacteria, 9th Edition, isolates were characterized for different biochemical assays. The tests were carbohydrate fermentation, catalase test, mobility test, citrate utilization, triple sugar iron, indole production, MR-VP test, peptone nitrate reduction, ammonia production, urea hydrolysis, gelatin hydrolysis and lipid hydrolysis 3,43.

Production of Phytohormones

24 hour old explants were allowed to develop in tryptophan culture at 30 °C for 24 hours in order to measure the quantity of Indole Acetic Acid (IAA) produced in each isolate using Salkowski’s reagent. After incubation, the broth was centrifuged, and Salkowski reagent 2 ml were combined with 1 ml of the supernatant. IAA generation is shown by the colour shift and absorption at 540 nanometers. Before to using the set in potted culture studies, each isolate was maintained in three sets 44.

Results and Discussion

In this present study, 50 isolates were isolated from different Rhizome Regions of the roots and soil samples. Samples were taken from 10 districts of Saurashtra region – Rajkot 19, Junagadh 9, Amerali 5, Botad 5, Morbi 2, Dwarka 2, Kutch 3, After Ahemdabad 2, Surat 2 and Vadodara 1 are presented in Table 1

Characteristics of the Colony

All 50 isolates were morphologically classified by Gram staining based on their characteristics such as shape, size, margin texture, elevation, and opacity. Of these isolates, 44 strains of bacteria were gram-negative, all of which were circular in shape with an entire margin and smooth texture, followed by a predominantly small, but some are medium sized and slightly raised or flat elevation. 14 colonies were opaque white, 32 colonies were transparent and 4 colonies were translucent. 6 Strain of bacteria were Gram Positive.

Biochemical characteristics

Models: – S-2, S-3, S-7, S-11, S-12, S-13, S-15, S-16, S-17, S-21, S-27, S- 29, S-30, S-41, S-46 are portable Fermenting sugars such as glucose, fructose, lactose, mannitol, it hydrolyzes gelatin, and urea, they can also produce H2S, indol and ammonia. The results are shown in Table 3. These isolates were then screened for potted culture experiments.

Production of Phytohormones

Salkowski reagent was used to assess the IAA generation of 50 isolates at 540 nm. Figure 4 displays the three isolates that produced the greatest IAA, S-27 190.19 g/ml, S-46 195.20 g/ml, and S-21 90.04 g/ml. The histogram’s X-axis and l-Y axis both display the number of isolates, shows the amount of IAA created by Isolate.

Table 1: shows isolates from Saurashtra region.

Click here to view Table

*Sample– Plant sample, Sample Code S- Sample, No.- Sample number, Plant Initials, Plant Numbers and City/Village Initials, City/Village-Sample collected, District

Table 2: Colony Characteristic of different isolates.

Sample +/- Shape Size Margin Texture Elevation Opacity
S1 -ve Round Small Entire Smooth Slight Raised Opaque
S2 -ve Round Small Entire Smooth Flat Transperant
S3 -ve Round Small Entire Smooth Slight Raised Transperant
S5 -ve Round Small Entire Smooth Slight Raised Transperant
S6 -ve Round Small Entire Smooth Slight Raised Opaque
S7 -ve Round Small Entire Smooth Flat Transperant
S9 -ve Round Small Entire Smooth Flat Transperant
S10 -ve Round Medium Entire Smooth Raised Transperant
S11 -ve Round Small Entire Smooth Slight Raised Transperant
S12 -ve Round Small Entire Smooth Slight Raised Transperant
S13 -ve Round Small Entire Smooth Flat Opaque
S14 -ve Round Small Entire Smooth Flat Transperant
S15 -ve Round Small Entire Smooth Flat Transperant
S16 -ve Round Small Entire Smooth Flat Transperant
S18 -ve Round Small Entire Smooth Flat Transperant
S19 -ve Round Small Entire Smooth Raised Opaque
S20 -ve Round Small Entire Smooth Slight Raised Transperant
S21 -ve Round Small Entire Smooth Slight Raised Transperant
S22 -ve Round Small Entire Smooth Slight Raised Opaque
S23 -ve Round Small Entire Smooth Flat Transperant
S24 -ve Round Small Entire Smooth Flat Transperant
S26 -ve Round Medium Entire Smooth Raised Transperant
S27 -ve Round Small Entire Smooth Slight Raised Transperant
S28 -ve Round Small Entire Smooth Slight Raised Opaque
S29 -ve Round Small Entire Smooth Flat Transperant
S30 -ve Round Small Entire Smooth Raised Opaque
S31 -ve Round Small Entire Smooth Flat Transperant
S32 -ve Round Small Entire Smooth Raised Transperant
S33 -ve Round Small Entire Smooth Raised Transperant
S34 -ve Round Small Entire Smooth Flat Opaque
S35 -ve Round Small Entire Smooth Slight Raised Transperant
S36 -ve Round Small Entire Smooth Slight Raised Transperant
S37 -ve Round Small Entire Smooth Slight Raised Opaque
S39 -ve Round Small Entire Smooth Raised Transperant
S40 -ve Round Medium Entire Smooth Raised Translucent
S41 -ve Round Medium Entire Smooth Raised Transperant
S42 -ve Round Small Entire Smooth Slight Raised Transperant
S43 -ve Round Small Entire Smooth Slight Raised Opaque
S44 -ve Round Small Entire Smooth Flat Transperant
S46 -ve Round Small Entire Smooth Slight Raised Transperant
S47 -ve Round Small Entire Smooth Slight Raised Transperant
S48 -ve Round Small Entire Smooth Slight Raised Opaque
S49 -ve Round Small Entire Smooth Flat Transperant
S50 -ve Round Small Entire Smooth Flat Transperant

* S-Sample number, +ve – Gram Positive Bacteria and –ve – Gram Negative Bacteria

Table 3: Shows Biochemical Characterization of different Isolates

Table 3: Shows Biochemical Characterization of different Isolates

Click here to view Table

*TSI- Triple Sugar Iron, GPB- Glucose Phosphate Broth, MR- Methyl Red VP- Voges Proskauer, TRP-Tryptophan, PNB- Peptone Nitrate Broth

Figure 1: Shows IAA (Indole Acetic Acid) Produced by isolates

Click here to view Figure

Discussion

One of the most well researched plant growth-promoting bacteria, Azospirillum, is found specifically in the rhizomes and intercellular regions of cereal roots and other plant roots.43 The favourable benefits of this bacterium on plant development have been demonstrated through a number of pathways indicated by plant-Azospirillum interactions. The concept of the multiple mechanism hypothesis was developed through the study of numerous phytohormones, plant regulators, nitrogen fixation, phosphate solubilizers, a wide range of molecules and enzymes, enhanced membrane activity, root system proliferation, increased water and mineral absorption, reduced pathogens, environmental stressors, and competition against pathogens. 12 The most significant agricultural crop in the world is wheat, which is farmed in a variety of habitats, from marshlands to desert areas. Since the 1970s, scientists have been examining the results of Azospirillum inoculating grass. 45 Azospirillum, one of 113 species in 35 plant families, is a soil bacterium that encourages plant development. 8 The number of primary root nodules dramatically increased when A. brasilense, an efficient generator of IAA, was applied to alfalfa seeds; this increase was associated with inoculum size. 11 One isolation (Sp1) and the second isolate (Sp2) revealed 99% similarity to Azospirillum brasilense and Azospirillum zeae, respectively, based on 16S rRNA sequence analysis. In a pot experiment, the impact of these two isolates on bread wheat was investigated. 46 The greatest obstacle to effective inoculation is the toxicity of pesticides employed in seed treatments. In order to avoid direct bacterial exposure to pesticides, we investigated different approaches to inoculating maize and wheat seeds in this work.47

Conclusion

The current study includes 50 isolates from the Saurashtra Area, of which 2 isolates, S-27 and S-46, were shown to produce the greatest IAA (Indole Acetic Acid) production when tested against Salkowski’s reagent. These 2 isolates will be examined for 16s rRNA sequencing as well as evaluated against pot cultures. In order to create bio-fertilizers and field characteristics, it can be employed. The Saurahtra area would be a better place to isolate species of Azospirillium sp., which might help improve numerous growth indices, mineral uptake, and water absorption.

Acknowledgment

The Authors are thankful to the Head of the Department of Microbiology and Biotechnology, Atmiya University, Rajkot for providing suggestion, infrastructure and facilities

Funding Sources

Sarvangi Rabara is thankful to Government of Gujarat for providing financial assistance under its ‘SHODH SCHEME’.

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