Article Type : Research Article
Authors : Prasad K
Keywords : Evaluation; Soybean; Temperature; Tropical soil; Bradyrhizobium japonicum
One
Kind Of Legume-Root Nodulating, Microsymbiotic Nitrogen-Fixing Bacterium Is
Called Bradyrhizobium Japonicum. The Bacterial Species Is One Of Many Rod-Shaped,
Gram-Negative Bacteria Known As Diazotrophic Bacteria; These Bacteria Fix
Nitrogen After Settling Inside The Legume (Fabaceae) Family's Root Nodules. The
Current Experiment Was Conducted To Collect Data On In Vitro Physiological
Temperature Tolerance Of Sixteen Bradyrhizobial Strains Isolated From Soybean
Root Nodules Collected From Various Soybean Growing Fields Of Bundi And Udaipur
Regions Of Rajasthan, India. The Extent Of Endurance Of Bradyrhizobial Strains
To Various Temperatures Was Investigated By Incubating The Bacterial Culture At
Different Temperatures Ranging From 250c - 550c. The Bradyrhizobial Growth In 20e
Broth Was Observed As Od540nm And Interpreted In Terms Of The Temperature
Tolerance Of The Strains. Results Indicated A Decline In Bacterial Growth With
The Elevated Temperature. At 400c, Five Bradyrhizobial Strains Namely Bj335-1, Bj335-2,
Bpk-1, Uj335-3 And Uj335-4 Showed A 5.09% To 19.45% Decline In Od540nm Compared
To The OD Values Recorded At 250c And Rest Of The Strains Showed 22.54% To 44.54%
Decrease. At 500c Only Two Strains Namely Bpk-3 And Uj335-1 Could Exhibit
Noticeable Growth In The 20e Broth While The Rest Of The Bradyrhizobial
Collection Exhibited Insignificant Growth And None Of The Strains Was Able To
Tolerate The Temperature Beyond 550c. However, The Uj335-1 Strain Was Still
Tolerant At 550c Temperature Showing Noticeable Turbidity In The 20e Broth. The
Present Study On The Temperature Response Of Bradyrhizobia Could Be Useful In
Identifying Better Strains Suited To Soils Having Elevated Temperature; A
Uniform Feature As Also Exists In The Soybean Cultivation Region Of Rajasthan, Indian.
Microorganisms, particularly microscopic organisms,
increase soil richness through supplement reusing like carbon, nitrogen,
sulfur, phosphorus, iron and potassium. Microorganisms deteriorate dead natural
matter and deliver basic mixtures in the dirt, which can be taken up by plants.
Nitrogen-fixing bacteria (NFB) fix atmospheric nitrogen and increase the
nitrogen content in the soil, which can be readily absorbed by plants and
improve growth and productivity. They likewise further develop soil construction
and increase the water-holding capacity of the soil. A kind of soil bacteria
known as rhizobia causes root nodules in legume roots by infecting the roots.
Rhizobia are soil-dwelling microorganisms that, upon infection, cause legumes
to develop nodules where they fix atmospheric nitrogen gas (N2) and convert it
into a form of nitrogen that is more easily used. The legume uses the nitrogen
that is exported from the nodules to thrive. After the legume dies, the
disintegration of the nodule releases the rhizobia back into the soil, where it
can either survive on its own or infect a new legume host. One sort of
legume-root nodulating, microsymbiotic NFB is called Bradyrhizobium japonicum.
B. japonicum is coated with legume seed to increase root development and improve
crop yields, particularly in areas where the bacterium is not native. Often the
inoculation is adhered to the seeds before planting using a jaggery/gum
solution. They are a widespread type of soil-dwelling bacteria that may work in
symbiotic partnerships with types of leguminous plants where they fix nitrogen
in exchange for carbohydrates from the plant. Like other rhizobia, they could
fix atmospheric nitrogen into forms readily available for other organisms to
use. Since 1957, a strain of B. japonicum has been utilized as a model
organism. It is widely used to study molecular genetics, plant physiology, and
plant ecology due to its relatively superior symbiotic nitrogen-fixation
activity with soybeans compared to other rhizobia species. The primary goal of
agricultural microbiology is to comprehensively explore the interactions
between beneficial microbes (BMs) such as bacteria and fungi with crops. It
also deals with the microbiology of soil fertility (SF), such as microbial
degradation of organic matter (OC) and soil nutrient transformations (SNT).
Healthy populations of beneficial bacteria/fungi can help suppress pathogens
and pests, promote plant growth (PG), and increase quality yield. The growth
and activity of the N2 fixing plants are restricted by several environmental
conditions. The process of fixing N2 in the Rhizobium-legume symbiosis is
strongly correlated with the host plant's physiological state. Within the soil,
rhizobia frequently encounters various stresses that affect their growth, the
initial steps of symbiosis, and the efficiency of nitrogen fixation [1-3].
Among several environmental conditions, which are limiting factors, water
stress, salinity, temperature extremes and pH stress are the most problematic.
A competitive and persistent rhizobial strain is not expected to express its
full capacity for nitrogen fixation (NF) as these limiting factors impose
limitations on the vigour of the host legume [4,5]. Since rhizobial populations
vary in their tolerance to major environmental factors, screening for tolerant
strains has been pursued by several researchers [2,6-17]. One of the main
obstacles to BNF in legume crops is the high soil temperature found in tropical
areas. Temperatures in these regions average above 400C may affect symbiotic
relationships, nitrogen content and plant production [18,19]. Therefore,
temperature tolerance findings of rhizobia are imperative to selecting
heat-tolerant strains for tropical conditions. Michaels [20]. found
heat-inducible proteins in heat-sensitive and heat-tolerant strains and
demonstrated acquired thermotolerance in the heat-tolerant strain Rhizobium
tropici CIAT899. Bayoumi [21]. additionally explored the impacts of various
abiotic factors (acridity, saltiness, nitrate, and temperature) on the development
pace of root-knob microbes (Rhizobium and Bradyrhizobium) strains in vitro and
announced that strains separated from Vicia faba L., Coronilla varia L.
furthermore, Lupinus albus L. shown a huge variety in resilience of the
previously mentioned factors. Pinto [22]. Evaluated the effects of heat on
growth, survival, symbiotic performance, and genomic modifications in effective
R. tropici and R. leguminosarum bv. phaseoli strains isolated from Cerrado
soils and suggested that the strategies used in their study to evaluate
survival capacity, N2 fixation performance and genetic stability after thermal
stress could be useful in selecting efficient and stable Rhizobium strains to
be used as inoculum for bean plant cultivation in tropical soil conditions. Given
the above discussion, further work is still needed to increase our knowledge of
the rhizobial ecology under suboptimal environmental conditions such as
elevated temperature which may constitute a strategy for improving
legume-rhizobium symbiosis in adverse environments of various soybean growing
regions of Rajasthan, India. With this aim in mind, a current study was
conducted, and data were collected on the in vitro physiological temperature
tolerance of sixteen authenticated bradyrhizobial strains.
Isolation,
characterization, authentication, and nomenclature of Bradyrhizobial strains
Isolate of B. japonicum strains were obtained from root nodules of field-grown soybean plants (cv. PK 472) collected from Adaptive Trial Centre (ATC), Bundi, Rajasthan, India (Figure 1). The serial dilution agar plate method as described in Somasegaran and Hoben [23] was employed with 20E medium [24] for Bradyrhizobium strain isolation. Isolates were streak and purified on the same medium and the purified isolates were subjected to an authentication test in growth pouches (procured from Mega International, USA) under controlled environmental conditions (day length, 14 h; temperature, 28±1°C, light intensity, 12000 lux; humidity, 70-80%). Sixteen authenticated strains were maintained as frozen glycerol stocks at - 40°C. These strains were nomenclature as their first letter depicting the region of origin (B- Bundi; U- Udaipur) and a numeric figure given at the end showing the specific strain assigned number. J335 and PK represent the soybean cultivars JS 335 and PK 472 respectively (Table 1).
Bradyrhizobial culture suspensions were inoculated in tubes containing 20E broth. These tubes were incubated at various temperatures ranging from 25 0C to 55 0C. The bacterial growth at various temperatures was measured by recording optical density at 540 nm using a Systronics model 106 spectrophotometer (Table 1). In this experiment, 28 ±10C was taken as ‘control’ or ‘reference’ temperature of thermal exposure.
The extent of tolerance of bradyrhizobial strains to various temperatures was studied by incubating the bacterial culture at different temperatures ranging from 250C to 550C. Comparative growth of the sixteen bradyrhizobial strains in terms of OD540nm at 550C temperature has been shown in Figure 3. It is evident from Table 1 and Figure 2 that there was a decline in bacterial growth with the elevated temperature. At 250C maximum growth (0.945) was shown by UJ335-5 while minimum growth (0.589) was shown by BPK-1 and BPK-6. At 280C and 300C luxuriant growth ranging from 0.874 -1.304 OD540nm and 0.845-1.187 OD540nm respectively was recorded for the studied bradyrhizobial strains. At 350C a gradual decrease in OD540nm compared to 300C was noticed and the maximum OD540nm (0.989) at this temperature was recorded for UJ335-1 while minimum OD540nm (0.675) was observed for BPK-6.
At 400C, five bradyrhizobial strains namely BJ335-1, BJ335-2, BPK-1, UJ335-3 and UJ335-4 showed a 5.09% to 19.45% decline in OD540nm compared to the OD values recorded at 250C and rest of the strains showed 22.54% to 44.54% decrease. At 450C OD540nm ranged from 0.306 – 0.521. At 500C, this decrease in OD values was more obvious where the OD values ranged from 0.176 – 0.323 and only two strains namely BPK-3 and UJ335-1 could exhibit noticeable growth (0.265 and 0.323 respectively) in the 20E broth. However, at 550C temperature a drastic decrease in terms of insignificant OD540nm was encountered which ranged from 0.006 – 0.021 for fifteen bradyrhizobial strains. However, UJ335-1 strain was still tolerant at this temperature showing noticeable turbidity (0.178 OD540nm) in the 20E broth (Figures 2,3). Several studies have reported that rhizobial growth is adversely affected by high soil temperature [14,15] [26-28]. Consequently, temperature tolerance studies of sixteen bradyrhizobial strains were conducted. Parallel to these studies, in the present investigation, a decline in bradyrhizobial growth with increased temperature was also realized. The optimum temperature range for bradyrhizobial growth in the current study was 280C-300C. A few past Scientists likewise affirmed this finding by detailing that the ideal temperature for the development of root nodulating bacteria ranged from 25°C-30°C [29,30]. However, the inhibitory effect of elevated temperature (45°C) was visible on the growth response of bradyrhizobia since moderate growth was recorded for majority of the strains. This result corroborates the previous findings of Werner [31] (1992) who stated that survival of the majority of Bradyrhizobium strains is strongly reduced above 40oC. Moreover, LaFavre and Eaglesham also reported that the nodulation of soybean was markedly inhibited at 42°C and 45°C for 12 hours and 9 hours days. UJ335-1 was found to be the highest temperature-tolerant strain in the current study, which showed considerable growth even at a temperature as high as 550C. However, no strain could survive at temperatures beyond 550C. On the other hand, Mahobia and Mahna [13] while characterizing Prosopis rhizobia reported that all the strains could tolerate temperatures up to 550C.
Figure 1: Location map of Soybean cultivation area at Bundi, Rajasthan, India.
Figure 2: Temperature tolerance of sixteen bradyrhizobial strains (columns showing OD540nm values; 1-250C, 2-280C, 3-300C, 4-350C, 5-400C, 6-450C, 7-500C, 8-550C).
Figure 3: Comparison of sixteen bradyrhizobial strains with regard to high temperature (550C) tolerance.
Table
1: Effect of temperature
on growth of sixteen bradyrhizobial strains of soybean.
Brady-rhizobial strains |
Range of temperature
|
||||||||
|
|||||||||
25oC |
28oC |
30oC |
35oC |
40oC |
45oC |
50oC |
55 oC |
||
BJ 335-1 |
0.663±0.023 |
0.985±0.022 |
0.978±0.034 |
0.773±0.047 |
0.534±0.032 |
0.427±0.023 |
0.212±0.020 |
0.021±0.003 |
|
BJ 335-2 |
0.673±0.034 |
0.937±0.041 |
0.968±0.043 |
0.749±0.011 |
0.545±0.017 |
0.428±0.030 |
0.203±0.017 |
0.016±0.002 |
|
BPK-1 |
0.589±0.034 |
0.896±0.045 |
0.879±0.032 |
0.713±0.034 |
0.489±0.029 |
0.328±0.047 |
0.201±0.019 |
0.011±0.001 |
|
BPK-2 |
0.743±0.045 |
0.892±0.015 |
0.886±0.012 |
0.689±0.008 |
0.412±0.050 |
0.310±0.012 |
0.213±0.023 |
0.017±0.003 |
|
BPK-3 |
0.739±0.046 |
0.923±0.066 |
0.905±0.049 |
0.836±0.048 |
0.525±0.043 |
0.435±0.042 |
0.265±0.015 |
0.019±0.002 |
|
BPK-4 |
0.678±0.076 |
0.957±0.026 |
0.958±0.021 |
0.786±0.087 |
0.489±0.065 |
0.321±0.041 |
0.178±0.011 |
0.008±0.001 |
|
BPK-5 |
0.708±0.057 |
1.048±0.048 |
1.036±0.050 |
0.867±0.027 |
0.467±0.034 |
0.343±0.022 |
0.176±0.019 |
0.006±0.001 |
|
BPK-6 |
0.589±0.011 |
0.874±0.039 |
0.845±0.093 |
0.675±0.048 |
0.398±0.029 |
0.306±0.012 |
0.201±0.027 |
0.014±0.002 |
|
BPK-7 |
0.698±0.038 |
0.993±0.043 |
0.978±0.051 |
0.853±0.077 |
0.447±0.038 |
0.355±0.017 |
0.226±0.028 |
0.017±0.003 |
|
BPK-8 |
0.766±0.059 |
0.948±0.048 |
0.939±0.017 |
0.812±0.094 |
0.527±0.041 |
0.426±0.038 |
0.256±0.021 |
0.019±0.002 |
|
UJ 335-1 |
0.945±0.049 |
1.304±0.023 |
1.187±0.018 |
0.989±0.083 |
0.637±0.055 |
0.521±0.048 |
0.323±0.029 |
0.178±0.014 |
|
UJ 335-2 |
0.732±0.044 |
1.065±0.033 |
0.984±0.051 |
0.824±0.043 |
0.567±0.034 |
0.455±0.038 |
0.212±0.018 |
0.006±0.000 |
|
UJ 335-3 |
0.767±0.050 |
0.973±0.019 |
0.964±0.073 |
0.882±0.098 |
0.668±0.056 |
0.479±0.038 |
0.234±0.010 |
0.008±0.001 |
|
UJ 335-4 |
0.609±0.037 |
0.968±0.036 |
0.958±0.082 |
0.806±0.099 |
0.578±0.066 |
0.463±0.043 |
0.204±0.016 |
0.010±0.001 |
|
UJ 335-5 |
0.879±0.044 |
1.217±0.067 |
1.117±0.043 |
0.911±0.048 |
0.611±0.040 |
0.465±0.014 |
0.223±0.017 |
0.011±0.002 |
|
UJ 335-6 |
0.749±0.012 |
1.113±0.039 |
1.006±0.088 |
0.887±0.101 |
0.534±0.027 |
0.421±0.023 |
0.212±0.011 |
0.016±0.003 |
|
*Data indicate mean value of three replicates: ± standard error. |
Overall evaluation of the data showed that the growth of bradyrhizobia decreased with increasing temperature. All the investigated bradyrhizobia strains grew abundantly at temperatures between 28°C and 30°C. At 40°C, at least nine bradyrhizobia strains showed a significant decrease in OD values ranging from 27.87% to 44.54% compared to the OD values at 25°C. At 50°C, only two strains, BPK-3 and UJ335-1, were able to show significant growth in 20E broth, while the rest of the bradyrhizobia collection showed only slight growth and none of the strains could tolerate temperatures above 55°C. These temperature-tolerant strains can also be selected to evaluate the possibility of symbiosis under elevated temperature in field conditions, a common trait found in various soybean-growing regions of Rajasthan, India.
The author declares
no financial support for the research, authorship, or publication of this
article.
Author contributions
The author
declare that the author contributed, approve of this work, and take full
responsibility.
Conflict of interest
The author
declares no conflict of interest.
Data availability
statement
Data supporting
these findings are available within the article.
Institutional
Review Board Statement
Not applicable.
Informed Consent
Statement
The author
declare that no human participants were involved in this study. Sample
availability the author declare that no physical samples were used in this
study.
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