Author:
Prashant Singh* and Neeraj Kumar Dubey
Journal Name: Biological Forum – An International Journal, 16(11): 102-105, 2024
Address:
*Department of Botany, Rashtriya P.G College Jamuhai, Jaunpur (Uttar Pradesh), India.
(Corresponding author: Prashant Singh*)
DOI: -
Among the Poaceae family, sugarcane stands out commercially. This species is a member of the Saccharum family and has its origins in Southeast Asia and South Asia. There are currently Saccharum officinarum, spontaneum, robustum, sinense, barberi, and edule are the six species that make up the genus Saccharum (Singh et al., 2020). The majority of these changes occurred in the twenty-ninth century as a result of several taxonomy revisions. Modern sugarcane cultivars are the product of hybridization between different species; most are 90% S. offcinarum and 10% S. spontaneum. This type of squash is classified as Saccharum spp. In 2017, the Americas accounted for 55.7% of global sugarcane production, while Asia accounted for 37.2%. With 758 Mt, or 41% of the global total, produced in 2017, Brazil surpassed all other countries as the top sugarcane producer. With respective contributions of 306, 104, 103, 73, and 57 metric tons (Mt) of sugarcane, Thailand, India, China, and Mexico all play a substantial role in the global supply. This culture's economic relevance is affected by its various functions. Sugar and cane molasses, two byproducts of sugarcane processing, are widely used in Brazil as both food and animal feed, in addition to being a key ingredient in ethanol. The versatile nature of sugarcane means that production will likely keep going up. There are a lot of different genera and species of diazotrophic plant growth-promoting bacteria that may be found in sugarcane (Taulé et al., 2016). Some examples are Burkholderia, Azotobacter, and Azospirillum. Another species is Gluconacetobacter diazotrophicus, which is basically Acetobacter diazotrophicus. Research in this field has been intensified by Brazilian scientists following the finding that G. diazotrophicus other cultures benefit from sugarcane-associated diazotrophic bacteria. PAL5T, HCC10, HRC54, CBAmC, Azospirillum amazonense, Paraburkholderia tropica, and Herbaspirillum rubrisubalbicans. To test the effects on sugarcane plant growth, PPe4T were introduced into the plant's root system (dos Santos et al., 2019).
It is impossible to exaggerate sugarcane's economic and industrial significance. Whether it's hot and dry at sea level or chilly and rainy at higher altitudes, this plant can be found in tropical and subtropical regions. Sugar isn't the only valuable thing that comes out of sugarcane. Other things like ethanol, bagasse, press mud, and molasses are also produced, along with chemicals, plastics, paints, and synthetics, which are essential resources for many other industries.
The host plant can benefit from PGPR-plant interactions in a number of ways, including colonizing bacteria, plant growth-promoting chemicals produced by rhizobacteria, antifungal and antibacterial substances, and biocontrol agents (James et al., 1997). All of the aforementioned procedures were found to be cooperating in other cases.
LITERATURE REVIEW
The adsorption of phosphate (P) to soil colloids makes it an essential nutrient for high sugarcane yields all through the crop's life cycle. "Some plant growth-promoting bacteria (PGPBs) have the potential to increase plant phosphorus availability and produce phytohormones that boost crop development, quality", and yield (Rosa et al., 2022). Consequently, this study set out to investigate how PGPB inoculation and phosphate fertilisation affected the yield, technical quality, "nitrogen (N) and phosphorus (P) contents of sugarcane leaves. The experiment took place in Ilha Solteira in São Paulo, Brazil. Eight inoculations of three species of PGPBs (Azospirillum brasiliense, Bacillus subtilis, and Pseudomonas fluorescence) and five phosphorus rates (0, 25, 50, 75, and 100 percent of the recommended P2O5 rate) were utilized in this investigation, which included three replications of the randomized block design. Following inoculation with B. subtilis and P." fluorescens, sugarcane showed an increase in leaf P content. Results from sugarcane stalk inoculation and P2O5 rates are correlated. Fertilizers that are either too much or too little phosphate are bad for sugarcane crops, regardless of whether growth-promoting microorganisms are used. We suggest a combination of A. brasilense and B. subtilis inoculation with 45 kg ha-1 of P2O5 for increased stalk yield. As a result of its increased sugar output and 75% reduction in the allowed P2O5 rate, this treatment is a better and more sustainable option for sugarcane crop development.
Sugarcane Genotypes' Growth and Yield. Sugarcane accounts for over 75% of all sugar produced across the globe. It is an economically viable biofuel and biomass crop that contributes significantly to the manufacture of bioethanol and the generation of electricity (World Sugar Statistics, 2014). When compared to the breeding histories of other key broad-acre crops, sugarcane's breeding history is rather short. Sugarcane breeding activities all around the world are focused on improving disease resistance, cane output, and sugar content in order to achieve these aims (Oliveira et al., 2003).
Cultivated in various tropical and subtropical climates across the world, it is a significant economic crop. with the majority of it being farmed in the United States (FAO, 2014). The genetic engineering (GE) interaction is a substantial source of diversity in sugarcane yield in many breeding programmes, and it has the potential to have a large impact on breeding programme selection in the future (Bartz, 2014). It seems that gene-location (GL) links are more important for cane yield than gene-year (GY) or gene locus/year (GLY) relationships in some studies. However, it should be noted that this is not the case in all of them. Increasing our understanding of the environmental and genetic factors that influence GE interaction might aid in the creation of more targeted selection approaches, however little research and major results have been made in this area thus far. Sugarcane genetic interactions were not found to be impacted by soil type or weather conditions in a recent assessment of soil and meteorological characteristics effecting sugarcane development. The study was conducted across and inside China and Australia and found no evidence of genetic interactions.
Sugarcane Producing Regions in India. Researchers from the AICRP-Sugarcane network have had a significant impact on sugarcane yield and output in Brazil. "After Brazil, India is the world's second-largest producer of sugarcane (15.81%) and sugar in addition to its dominance as the world's greatest" producer and consumer of sugar (15.93 percent), China is also the world's seventh largest exporter of the sweetener (2.80 percent) (2015- 16 - Aprilto January) (Leite et al., 2014). Productivity has risen from 48.0 tons/hectare (1970-71) to roughly 70 tonnes per hectare (1990-91). (2015-16). In contrast, cane output has increased from 126 million tonnes in the year 1970-71 to 341 million tonnes in the current year (2015-16).
“On the Root Colonization of G. Fasciculatumand the Growth of Sugarcane”, G. Diazotrophicus Has an Impact. Filling cement pots with sterilised sand and soil (1:1) was done. A thin, homogeneous coating of 50 g pot-1 G. fasciculatum soil-based root inoculums was buried two centimetres below the soil's surface. At two setts pot-1, sugarcane setts of the var (CoC 24) were planted. “The setts were treated with a culture suspension of G. diazotrophicus containing 1 107 CFU ml-1” prior to planting. With no G. diazotrophicus or G. fasciculatum, a total control was maintained.
When G. diazotrophicus is employed as an inoculant against “G. fasciculatum, the incidence of red rot disease” decreases. “G. fasciculatum root-based soil inoculums at 50 g pot-1 were applied two centimetres below the soil surface as a thin film” of homogeneous thickness in cement pots of 20 kilogramme capacity. CoC 24 vartwo .'s budded sugarcane sets (pot-one) were planted and maintained.
Qualitative and quantitative investigation of sugarcane root exudates anionic fraction
“G. diazotrophicus and AM fungi impact sugarcane growth and yield”
Experiment on sugarcane yield and development with G. diazotrophicus and AM fungus injected with varying concentrations of inorganic N and P fertilisers in the field.
Objective of the Study
1. To examine Diazotrophic Bacteria Sugarcane Crops for Drought Tolerance Nature.
Exclusion and Control of Am Fungi In Sugarcane Farms. This experiment demonstrated that there are considerable variations in root colonization percentage and spore amount 100g-1 soil. Twenty locations in the Atarahi District were used to collect and categorize soil samples from sugarcane rhizospheres. The results showed that eight of the samples were clay loam. The organic carbon content ranged from 0.36 to 0.77 percent in each sample, while the bioavailable phosphorus concentration was 11.18 to 21.10 kg/ha.
Atkadpur | Clay loam | 8.0 | 0.46 | 0.70 | 13.24 | 50.0 | 100.5 | |
Baghmurtza | Sandyclay | 8.5 | 0.53 | 0.76 | 19.38 | 32.0 | 65.0 | |
Bans Gopalpur | Sandy clay | 7.4 | 0.32 | 0.47 | 19.10 | 39.2 | 80.5 | |
Barrre Patti | Sandy loam | 7.3 | 0.40 | 0.36 | 21.10 | 35.0 | 86.0 | |
Bhakura | Sandy clay | 8.44 | 0.50 | 0.71 | 12.00 | 29.8 | 67.0 | |
Baboopur | Sandy clay | 8.67 | 0.48 | 0.69 | 16.00 | 30.0 | 80.0 | |
Alamgirpur | Clay loam | 8.94 | 0.48 | 0.72 | 14.00 | 40.5 | 84.0 | |
Chak Pahalawan Tahir | Clay loam | 8.64 | 0.48 | 0.62 | 18.00 | 40.0 | 80.0 | |
Chaka Banki | Sandy clay | 8.05 | 0.50 | 0.65 | 11.00 | 41.3 | 80.0 | |
Chaktali | Sandy clay | 8.86 | 0.50 | 0.61 | 13.00 | 34.9 | 67.0 | |
Baijapur | Sandy clay | 8.27 | 0.50 | 0.49 | 12.00 | 34.5 | 67.0 |
Table 2: Different AM fungus isolates from sugarcane rhizosphere soil samples were discovered and described.
Sr. No. | Characters | Glomus mosseae | Glomus fasciculatum | Glomus versiforme | Acaulospora Laevis | Gigaspora margarita |
1. | Size of spore | 120 | 100-120µm | 125-150 µm | 400 µm | 200-300 μm |
2. | Spore shape | Globose | Globose hypogeous | Globose | Globose | Ectocarpic |
3. | Colour of spore | Yellow to brown | Yellow to reddish brown | Yellow to brown | Outer wall - brown Inner wall- Hyaline Ellipsoid | White when young and slightly yellowish at maturity |
4. | Sporocarp | Present | Present | Present | Present | Absent |
5. | Thickness of spore wall | 3-4 µm | 4-14 µm | 3-4 µm | 4-8 µm | > 20µm |
6. | Subtending hyphae | Cylindric flared | Absent | Cylindric or flared | Not observable | Bulbous 30-50 µm |
Table 3: Different AM fungus isolates from sugarcane rhizosphere soil samples were discovered and described.
Sr. No. | Soil texture | Total AM fungal spore population per 100 g of soil in each soil types | Glomus mosseae | Glomus fasciculata | Glomus vermiform | Acaulospora laevis | Gigaspora margarita |
1. | Sandy Clay | 82.0 | 16.0 | 38.0 | 5 | 9 | 14 |
2. | Sandy loam | 80 | 16.0 | 34 | 6 | 10 | 14 |
3. | Clay loam | 102.0 | 22.0 | 48.0 | 7 | 11 | 14 |
4. | clay | 78.0 | 16.0 | 38.0 | 5 | 9 | 10 |
Table 4: Sugarcane var. CoC 24 was used to test several AM fungus species under pot culture conditions.
Sr. No. | Am fungal inoculation | Percent root colonization | Spore number 100g of rhizosphere soil | Acid phosphates activity (µg/24 hrs. 10g¹ of root) | Alkaline phosphates activity (µg/24 hrs-1 10g¹ of root) | ||||||||
Sampling period in days | Sampling period in days | Sampling period in days | Sampling period in days | ||||||||||
1. | Glomus mosseae | 42.00 | 54.90 | 61.20 | 144.60 | 164.90 | 175.00 | 26.090 | 27.60 | 28.90 | 24.30 | 26 | 25.90 |
2. | Glomus fascicula tum | 53.60 | 61.30 | 78.20 | 151.90 | 168.30 | 180. | 27.30 | 28.60 | 28 | 25 | 27.90 | 26.30 |
3. | Glomus versifor me | 26.30 | 39.60 | 46.20 | 128.30 | 156 | 165.60 | 23.60 | 25.90 | 26.60 | 21.90 | 21.30 | 21.00 |
4. | Acaulos pora laevis | 38.60 | 49.30 | 57 | 139 | 163.90 | 170 | 25.30 | 26.30 | 28.90 | 23 | 24 | 23.30 |
5. | Gagaspora margarit | 30.30 | 42 | 52.60 | 130.90 | 156.30 | 164.30 | 24 | 26 | 28.60 | 21.30 | 22.60 | 21.60 |
SE | 2.59 | 2.12 | 2.02 | 2.27 | 0.52 | 1.14 | 0.31 | 0.17 | 0.33 | 0.45 | 0.47 | 0.61 | |
CD (p=0.05) | 7.24 | 6.03 | 5.75 | 6.49 | 1.50 | 3.28 | 0.89 | 0.51 | 1.95 | 1.30 | 1.35 | 1.76 | |
Control of sugarcane red rot using G. diazotrophicus and G. fasciculatum. There was an increase in the incidence of red rot disease in both the individual inoculations of G. diazotrophicus and the combination inoculations of G. fasciculatum, as reported in (Table 5). G. diazotrophicus and “G. fasciculatum inoculation greatly decreased the incidence of red rot disease”. Comparatively, in comparison to the individual inoculations of G. diazotrophicus and fungus AM.
Patients who received both G. diazotrophicus and G. fasciculatum on 180 DAP had the greatest decrease in illness incidence “(67.00%), followed by those who received G. diazotrophicus alone (42.22) and G. fasciculatum only (25.67).”
Table 5: “Control of red rot disease in sugarcane” by G. diazotrophicus and G. fasciculatum inoculation alone and in combination.
Sr. No. | Treatments | Occurrence of disease incidence % | Percent reduced on over control | ||
Sampling period in days | Sampling period in days | ||||
120 | 180 | 120 | 180 | ||
1. | Uninoculated control | 0.00 | 0.00 | 0.00 | 0.00 |
2. | Celletotrichum falcatum alone | 67 | 43.02 | 0 | 0 |
3. | Celletotrichum falcatum + G diazotrophicus | 38 | 26.84 | 43.45 | 42.22 |
4. | Celletotrichum falcatum + G fasciculatum | 44.62 | 34.25 | 35.62 | 25.67 |
5. | Celletotrichum falcatum + G fasciculatum + G diazotrophicus | 20 | 14.00 | 68.00 | 67.00 |
SE | 1.7411 | 1.3066 | |||
CD (p- 0.05) | 4.96 | 3.73 | |||
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