Review Article | Volume: 5, Issue: 6, Nov-Dec, 2017

Beneficial microbiomes: Biodiversity and potential biotechnological applications for sustainable agriculture and human health

Ajar Nath Yadav Rajesh Kumar Sunil Kumar Vinod Kumar TCK Sugitha Bhanumati Singh Vinay Singh Chauahan Harcharan Singh Dhaliwal Anil Kumar Saxena   

Open Access   

Published:  Nov 09, 2017

DOI: 10.7324/JABB.2017.50607
Abstract

The beneficial microbes plays an important role in medical, industrial, and agricultural processes. The precious microbes belong to different groups including archaea, bacteria, and fungi which can be sort out from different habitat such as extreme environments (acidic, alkaline, drought, pressure, salinity, and temperatures) and associated with plants (epiphytic, endophytic, and rhizospheric) and human. The beneficial microbes exhibited multifunctional plant growth promoting (PGP) attributes such as N2-fixation, solubilization of micronutrients (phosphorus, potassium and zinc), and production of siderophores, antagonistic substances, antibiotic, auxin, and gibberellins. These microbes could be applied as biofertilizers for native as well as crops growing at diverse extreme habitat. Microbes with PGP attributes of N2-fixation, P-, and K-solubilization could be used at a place of NPK chemical fertilizers. Agriculturally, important microbes with Fe- and Zn-solubilizing attributes can be used for biofortification of micronutrients in different cereal crops. The biofertilizers are an eco-friendly technology and bioresources for sustainable agriculture and human health. In general, the concentrations of micronutrient in different crops are not adequate for human nutrition in diets. Hence, consumption of such cereal-based diet may result in micronutrient malnutrition and related severe health complications. The biofortification approach is getting much attention to increase the availability of micronutrients, especially Fe and Zn in the major food crops. The beneficial microbes can be used as probiotic as functional foods for human health. Probiotics microbes such as Bifidobacterium, Lactobacillus, Methanobrevibacter, Methanosphaera, and Saccharomyces are increasingly being used as dietary supplements in functional food products. The microbes with beneficial properties could be utilized for sustainable agriculture and human health.


Keyword:     BiodiversityBiofortificationMalnutritionMicrobiomesProbiotic.


Citation:

Yadav AN, Kumar R, Kumar S, Kumar V, Sugitha TCK, Singh B, Chauahan VS, Dhaliwal HS, Saxena AK. Beneficial microbiomes: Biodiversity and potential biotechnological applications for sustainable agriculture and human health. J App Biol Biotech. 2017;5(6):45-57. DOI: 10.7324/JABB.2017.50607.

Copyright: Author(s). This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike license.

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Reference

1. DeLong, EF, Pace, NR. Environmental diversity of bacteria and archaea. Systmatic Biology. 2001; 50:470-478.

2. Saxena, AK, Kaushik, R, Yadav, AN, Gulati, S, Sharma, D. Role of archaea in sustenance of plants in extreme saline environments. In: 56th Annual Conference of Association of Microbiologists of India and International Symposium on “Emerging Discoveries in Microbiology”. 2015; Doi: 10.13140/RG.2.1.2073.9925.

3. Verma, P, Yadav, AN, Shukla, L, Saxena, AK, Suman, A. Hydrolytic enzymes production by thermotolerant Bacillus altitudinis IARI-MB-9 and Gulbenkiania mobilis IARI-MB-18 isolated from Manikaran hot springs. International Journal of Advanced Research. 2015; 3:1241-1250.

4. Kumar, M, Yadav, AN, Tiwari, R, Prasanna, R, Saxena, AK. Deciphering the diversity of culturable thermotolerant bacteria from Manikaran hot springs. Annals of Microbiology. 2014; 64:741-751.

5. Suman, A, Verma, P, Yadav, AN, Saxena, AK. Bioprospecting for extracellular hydrolytic enzymes from culturable thermotolerant bacteria isolated from Manikaran thermal springs. Research Journal of Biotechnology. 2015; 10:33-42.

6. Sahay, H, Yadav, AN, Singh, AK, Singh, S, Kaushik, R, Saxena, AK. Hot springs of Indian Himalayas: Potential sources of microbial diversity and thermostable hydrolytic enzymes. 3 Biotech. 2017; 7:1-11.

7. Yadav, AN, Sachan, SG, Verma, P, Saxena, AK. Prospecting cold deserts of north western Himalayas for microbial diversity and plant growth promoting attributes. Jounal of Bioscience and Bioengineering. 2015. 119:683-693.

8. Yadav, AN, Sachan, SG, Verma, P, Tyagi, SP, Kaushik, R, Saxena, AK. Culturable diversity and functional annotation of psychrotrophic bacteria from cold desert of Leh Ladakh (India). World Journal of Microbiology and Biotechnology. 2015; 31:95-108.

9. Yadav, AN, Verma, P, Sachan, SG, Saxena, AK. Biodiversity and biotechnological applications of psychrotrophic microbes isolated from Indian Himalayan regions. EC Microbiology. 2017; ECO.01:48-54.

10. Pandey, S, Singh, S, Yadav, AN, Nain, L, Saxena, AK. Phylogenetic diversity and characterization of novel and efficient cellulase producing bacterial isolates from various extreme environments. Bioscience, Biotechnology, Biochemistry. 2013; 77:1474-1480.

11. Saxena, AK, Yadav, AN, Rajawat, M, Kaushik, R, Kumar, R, Kumar, M, Prasanna, R, Shukla, L. Microbial diversity of extreme regions: An unseen heritage and wealth. Indian Journal of Plant Genetics Resources. 2016; 29:246-248.

12. Verma, P, Yadav, AN, Kazy, SK, Saxena, AK, Suman, A. Evaluating the diversity and phylogeny of plant growth promoting bacteria associated with wheat (Triticum aestivum) growing in central zone of India. International Journal of Current Microbiology and Applied Sciences. 2014; 3:432-447.

13. Verma, P, Yadav, AN, Khannam, KS, Mishra, S, Kumar, S, Saxena, AK, Suman, A. Appraisal of diversity and functional attributes of thermotolerant wheat associated bacteria from the peninsular zone of India. Saudi Journal of Biological Science. 2016; doi.org/10.1016/j.sjbs.2016.01.042

14. Yadav, S, Kaushik, R, Saxena, AK, Arora, DK. Diversity and phylogeny of plant growth‐promoting bacilli from moderately acidic soil. Journal of Basic Microbiology. 2011; 51:98-106.

15. Verma, P, Yadav, AN, Kazy, SK, Saxena, AK, Suman, A. Elucidating the diversity and plant growth promoting attributes of wheat (Triticum aestivum) associated acidotolerant bacteria from southern hills zone of India. National Journal of Life Sciences. 2013; 10:219-227.

16. Yadav, AN. Agriculturally Important Microbiomes: Biodiversity and Multifarious PGP Attributes for Amelioration of Diverse Abiotic Stresses in Crops for Sustainable Agriculture. Biomedical Journal of Scientific & Technical Research. 2017; 1: 1-4.

17. Verma, S, Varma, A, Rexer, K-H, Hassel, A, Kost, G, Sarbhoy, A, Bisen, P, Bütehorn, B, Franken, P. Piriformospora indica, gen. et sp. nov., a new root-colonizing fungus. Mycologia. 1998; 896-903.

18. Glick, BR. Introduction to Plant Growth-promoting Bacteria. In: Beneficial Plant-Bacterial Interactions. Springer, 2015; pp. 1-28.

19. Tilak, K, Ranganayaki, N, Pal, K, De, R, Saxena, A, Nautiyal, CS, Mittal, S, Tripathi, A, Johri, B. Diversity of plant growth and soil health supporting bacteria. Current Science. 2005; 89:136-150.

20. Yadav, AN, Verma, P, Kour, D, Rana, KL, Kumar, V, Singh, B, Chauahan, VS, Sugitha, T, Saxena, AK, Dhaliwal, HS. Plant microbiomes and its beneficial multifunctional plant growth promoting attributes. Journal of Environmental Science and Natural Resources. 2017; 3:1-8.

21. Verma, P, Yadav, AN, Kumar, V, Kumar, K, Dhaliwal, HS. Microbes mediated biofortification of wheat (Triticum aestivum L.) for micronutrients by Fe-chelating and Zn-solubilizing bacteria. In: Proceeding of National Conference on Advances in Food Science and Technology. 2017; pp. 199.

22. Suman, A, Yadav, AN, Verma, P. Endophytic Microbes in Crops: Diversity and Beneficial impact for Sustainable Agriculture. In: Singh DP, Abhilash PC, Prabha R (eds), Microbial Inoculants in Sustainable Agricultural Productivity, Research Perspectives. Springer-Verlag, India. 2016; pp. 117-143.

23. Holland, MA, Davis, R, Moffitt, S, O'Laughlin, K, Peach, D, Sussan, S, Wimbrow, L, Tayman, B. Using “leaf prints” to investigate a common bacterium. The American Biology Teacher. 2000; 62:128-131.

24. Hornschuh, M, Grotha, R, Kutschera, U. Epiphytic bacteria associated with the bryophyte Funaria hygrometrica: effects of Methylobacterium strains on protonema development. Plant Biology. 2002; 4:682-687.

25. Mukhtar, I, Khokhar, I, Sobia, M, Ali, A. Diversity of epiphytic and endophytic microorganisms in some dominant weeds. Pakistan Journal of Weed Science Research. 2010; 16:287-297.

26. Meena, KK, Kumar, M, Kalyuzhnaya, MG, Yandigeri, MS, Singh, DP, Saxena, AK, Arora, DK. Epiphytic pink-pigmented methylotrophic bacteria enhance germination and seedling growth of wheat (Triticum aestivum) by producing phytohormone. Antonie Van Leeuwenhoek. 2012; 101:777-786.

27. Dobrovol’skaya, T, Khusnetdinova, K, Manucharova, N, Golovchenko, A. Structure of epiphytic bacterial communities of weeds. Microbiology. 2017; 86:257-263.

28. Verma, P, Yadav, AN, Khannam, KS, Panjiar, N, Kumar, S, Saxena, AK, Suman, A. Assessment of genetic diversity and plant growth promoting attributes of psychrotolerant bacteria allied with wheat (Triticum aestivum) from the northern hills zone of India. Annals of Microbiology. 2015; 65:1885-1899.

29. Misaghi, I, Donndelinger, C. Endophytic bacteria in symptom-free cotton plants. Phytopathology. 1990; 80:808-811.

30. de Bruijn, FJ, Stoltzfus, JR, So, R, Malarvithi, PP, Ladha, JK. Isolation of endophytic bacteria from rice and assessment of their potential for supplying rice with biologically fixed nitrogen. In: Opportunities for Biological Nitrogen Fixation in Rice and Other Non-Legumes, J.K. Ladha, F.J. de Bruijn and K.A. Malik, eds. (Springer Netherlands), 1997; pp. 25-36.

31. Sturz, A, Christie, B, Matheson, B, Arsenault, W, Buchanan, N. Endophytic bacterial communities in the periderm of potato tubers and their potential to improve resistance to soil-borne plant pathogens. Plant Pathology. 1999; 48:360-369.

32. Rana, KL, Kour, D, Yadav, AN, Kumar, V, Dhaliwal, HS. Endophytic microbes from wheat: Diversity and biotechnological applications for sustainable agriculture. In: Proceeding of 57th Association of Microbiologist of India & International symposium on “Microbes and Biosphere: What’s New What’s Next”. 2016; pp. 453.

33. Yadav, AN, Rana, KL, Kumar, V, Dhaliwal, HS. Phosphorus solubilizing endophytic microbes: Potential application for sustainable agriculture. EU Voice. 2016; 2: 21-22.

34. Yadav, AN. Bacterial diversity of cold deserts and mining of genes for low temperature tolerance. Ph.D. Thesis, IARI, New Delhi/BIT, Ranchi. 2015; pp. 234, DOI: 10.13140/RG.2.1.2948.1283/2.

35. Shukla, L, Suman, A, Yadav, AN, Verma, P, Saxena, AK. Syntrophic microbial system for ex-situ degradation of paddy straw at low temperature under controlled and natural environment. Journal of Applied Biology and Biotechnology. 2016; 4:30-37.

36. Yadav, AN, Verma, P, Kumar, V, Sachan, SG, Saxena, AK. Extreme cold environments: A suitable niche for selection of novel psychrotrophic microbes for biotechnological applications. Advance in Biotechnology and Microbiology. 2017; 2:1-4.

37. Kumar, M, Yadav, AN, Tiwari, R, Prasanna, R, Saxena, AK. Evaluating the diversity of culturable thermotolerant bacteria from four hot springs of India. Journal of Biodiversity, Bioprospecting and Development. 2014; 1:1-9.

38. Yadav, AN, Sharma, D, Gulati, S, Singh, S, Kaushik, R, Dey, R, Pal, KK, Saxena, AK. Haloarchaea endowed with phosphorus solubilization attribute implicated in phosphorus cycle. Scientic Reports. 2015; 5: 12293.

39. Yadav, AN, Verma, P, Kumar, M, Pal, KK, Dey, R, Gupta, A, Padaria, JC, Gujar, GT, Kumar, S, Suman, A. Diversity and phylogenetic profiling of niche-specific Bacilli from extreme environments of India. Annals of Microbiology. 2015; 65:611-629.

40. Bowman, JP. Description of Cellulophaga algicola sp. nov., isolated from the surfaces of Antarctic algae. International Journal of Systematic and Evolutionary Microbiology. 2000; 50:1861-1868.

41. Reddy, G, Pradhan, S, Manorama, R, Shivaji, S. Cryobacterium roopkundense sp. nov., a psychrophilic bacterium isolated from glacial soil. International Journal of Systematic and Evolutionary Microbiology. 2010; 60:866-870.

42. Chaturvedi, P, Prabahar, V, Manorama, R, Pindi, PK, Bhadra, B, Begum, Z, Shivaji, S. Exiguobacterium soli sp. nov., a psychrophilic bacterium from the McMurdo Dry Valleys, Antarctica. International Journal of Systematic and Evolutionary Microbiology. 2008; 58:2447-2453.

43. Humphry, DR, George, A, Black, GW, Cummings, SP. Flavobacterium frigidarium sp. nov., an aerobic, psychrophilic, xylanolytic and laminarinolytic bacterium from Antarctica. International Journal of Systematic and Evolutionary Microbiology. 2001; 51:1235-1243.

44. Van Trappen, S, Vandecandelaere, I, Mergaert, J, Swings, J. Flavobacterium fryxellicola sp. nov. and Flavobacterium psychrolimnae sp. nov., novel psychrophilic bacteria isolated from microbial mats in Antarctic lakes. International Journal of Systematic and Evolutionary Microbiology. 2005; 55:769-772.

45. Margesin, R, Zhang, D-C, Frasson, D, Brouchkov, A. Glaciimonas frigoris sp. nov., a psychrophilic bacterium isolated from ancient Siberian permafrost sediment, and emended description of the genus Glaciimonas. International Journal of Systematic and Evolutionary Microbiology. 2016; 66:744-748.

46. Hirsch, P, Ludwig, W, Hethke, C, Sittig, M, Hoffmann, B, Gallikowski, C. Hymenobacter roseosalivarius gen. nov., sp. nov. from continental Antarctic soils and sandstone: bacteria of the Cytophaga/Flavobacterium/Bacteroides line of phylogenetic descent. Systmatic and Applied Microbiology. 1998; 21:374-383.

47. Lee, YM, Hwang, CY, Lee, I, Jung, Y-J, Cho, Y, Baek, K, Hong, SG, Kim, J-H, Chun, J, Lee, HK. Lacinutrix jangbogonensis sp. nov., a psychrophilic bacterium isolated from Antarctic marine sediment and emended description of the genus Lacinutrix. Antonie Van Leeuwenhoek. 2014; 106:527-533.

48. Shen, L, Liu, Y, Gu, Z, Xu, B, Wang, N, Jiao, N, Liu, H, Zhou, Y. Massilia eurypsychrophila sp. nov. a facultatively psychrophilic bacteria isolated from ice core. International Journal of Systematic and Evolutionary Microbiology. 2015; 65:2124-2129.

49. Gosink, J, Herwig, R, Staley, J. Octadecabacter arcticus gen. nov., sp. nov., and O. antarcticus, sp. nov., nonpigmented, psychrophilic gas vacuolate bacteria from polar sea ice and water. Systmatic and Applied Microbiology. 1997; 20:356-365.

50. Yakimov, MM, Giuliano, L, Gentile, G, Crisafi, E, Chernikova, TN, Abraham, W-R, Lünsdorf, H, Timmis, KN, Golyshin, PN. Oleispira antarctica gen. nov., sp. nov., a novel hydrocarbonoclastic marine bacterium isolated from Antarctic coastal sea water. International Journal of Systematic and Evolutionary Microbiology. 2003; 53:779-785.

51. Zhou, Z, Jiang, F, Wang, S, Peng, F, Dai, J, Li, W, Fang, C. Pedobacter arcticus sp. nov., a facultative psychrophile isolated from Arctic soil. International Journal of Systematic and Evolutionary Microbiology. 2012; 62:1963-1969.

52. López, NI, Pettinari, MJ, Stackebrandt, E, Tribelli, PM, Põtter, M, Steinbüchel, A, Méndez, BS. Pseudomonas extremaustralis sp. nov., a poly (3-hydroxybutyrate) producer isolated from an Antarctic environment. Current Microbiology. 2009; 59:514-519.

53. Zachariah, S, Kumari, P, Das, SK. Psychrobacter pocilloporae sp. nov., isolated from a coral, Pocillopora eydouxi. International Journal of Systematic and Evolutionary Microbiology. 2017; 66:5091-5098.

54. Auman, AJ, Breezee, JL, Gosink, JJ, Kämpfer, P, Staley, JT. Psychromonas ingrahamii sp. nov., a novel gas vacuolate, psychrophilic bacterium isolated from Arctic polar sea ice. International Journal of Systematic and Evolutionary Microbiology. 2006; 56:1001-1007.

55. Albert, RA, Waas, NE, Pavlons, SC, Pearson, JL, Ketelboeter, L, Rosselló-Móra, R, Busse, H-J. Sphingobacterium psychroaquaticum sp. nov., a psychrophilic bacterium isolated from Lake Michigan water. International Journal of Systematic and Evolutionary Microbiology. 2013; 63:952-958.

56. Zhang, D-C, Busse, H-J, Liu, H-C, Zhou, Y-G, Schinner, F, Margesin, R. Sphingomonas glacialis sp. nov., a psychrophilic bacterium isolated from alpine glacier cryoconite. International Journal of Systematic and Evolutionary Microbiology. 2011; 61:587-591.

57. Yadav, AN, Sachan, SG, Verma, P, Saxena, AK. Bioprospecting of plant growth promoting psychrotrophic Bacilli from cold desert of north western Indian Himalayas. Indian Journal of Experimental Biolology. 2016; 52:142-150.

58. Ravot, G, Magot, M, Fardeau, M-L, Patel, B, Prensier, G, Egan, A, Garcia, J-L, Ollivier, B. Thermotoga elfii sp. nov., a novel thermophilic bacterium from an African oil-producing well. International Journal of Systematic and Evolutionary Microbiology. 1995; 45:308-314.

59. Fardeau, M-L, Ollivier, B, Patel, B, Magot, M, Thomas, P, Rimbault, A, Rocchiccioli, F, Garcia, J-L. Thermotoga hypogea sp. nov., a xylanolytic, thermophilic bacterium from an oil-producing well. International Journal of Systematic and Evolutionary Microbiology. 1997; 47:1013-1019

60. Wagner, ID, Zhao, W, Zhang, CL, Romanek, CS, Rohde, M, Wiegel, J. Thermoanaerobacter uzonensis sp. nov., an anaerobic thermophilic bacterium isolated from a hot spring within the Uzon Caldera, Kamchatka, Far East Russia. International Journal of Systematic and Evolutionary Microbiology. 2008; 58:2565-2573.

61. Mori, K, Yamazoe, A, Hosoyama, A, Ohji, S, Fujita, N, Ishibashi, J-I, Kimura, H, Suzuki, K-I. Thermotogaprofunda sp. nov. and Thermotogacaldifontis sp. nov., anaerobic thermophilic bacteria isolated from terrestrial hot springs. International journal of systematic and evolutionary microbiology. 2014; 64:2128-2136.

62. Koeck, DE, Hahnke, S, Zverlov, VV. Herbinix luporum sp. nov., a thermophilic cellulose-degrading bacterium isolated from a thermophilic biogas reactor. International Journal of Systematic and Evolutionary Microbiology. 2016; 66:4132-4137.

63. Gaba, S, Singh, RN, Abrol, S, Yadav, AN, Saxena, AK, Kaushik, R. Draft genome sequence of Halolamina pelagica CDK2 isolated from natural salterns from Rann of Kutch, Gujarat, India. Genome Announcment. 2017; 5:1-2.

64. Yadav, AN, Verma, P, Kaushik, R, Dhaliwal, HS, Saxena, AK. Archaea endowed with plant growth promoting attributes. EC Microbiology. 2017; 8:294-298.

65. Giller, KE. Nitrogen fixation in tropical cropping systems, Cabi, 2001.

66. Elbeltagy, A, Nishioka, K, Sato, T, Suzuki, H, Ye, B, Hamada, T, Isawa, T, Mitsui, H, Minamisawa, K. Endophytic colonization and in planta nitrogen fixation by a Herbaspirillum sp. isolated from wild rice species. Applied and Environmental Microbiology. 2001; 67:5285-5293.

67. Boddey, RM, Urquiaga, S, Alves, BJ, Reis, V. Endophytic nitrogen fixation in sugarcane: present knowledge and future applications. Plant and Soil. 2003; 252:139-149.

68. Wei, C-Y, Lin, L, Luo, L-J, Xing, Y-X, Hu, C-J, Yang, L-T, Li, Y-R, An, Q. Endophytic nitrogen-fixing Klebsiella variicola strain DX120E promotes sugarcane growth. Biology and Fertility of Soils. 2014; 50:657-666.

69. Reis, VM, Teixeira, KRdS. Nitrogen fixing bacteria in the family Acetobacteraceae and their role in agriculture. Journal of Basic Microbiology. 2015; 55(8):931-49

70. Suman, A, Verma, P, Yadav, AN, Srinivasamurthy, R, Singh, A, Prasanna, R. Development of hydrogel based bio-inoculant formulations and their impact on plant biometric parameters of wheat (Triticum aestivum L.). International Journal of Current Microbiology and Applied Sciences. 2016; 5:890-901.

71. Singh, RN, Gaba, S, Yadav, AN, Gaur, P, Gulati, S, Kaushik, R, Saxena, AK. First, High quality draft genome sequence of a plant growth promoting and Cold Active Enzymes producing psychrotrophic Arthrobacter agilis strain L77. Standards in Genomic Sciences. 2016; 11:54.

72. Yadav, AN, Verma, P, Singh, B, Chauhan, VS, Suman, A, Saxena, AK. Plant Growth Promoting Bacteria: Biodiversity and Multifunctional Attributes for Sustainable Agriculture. Advance in Biotechnology and Microbiology. 2017; 5: 1-16.

73. Barra, PJ, Inostroza, NG, Acuña, JJ, Mora, ML, Crowley, DE, Jorquera, MA. Formulation of bacterial consortia from avocado (Persea americana Mill.) and their effect on growth, biomass and superoxide dismutase activity of wheat seedlings under salt stress. Applied Soil Ecololgy. 2016; 102: 80-91.

74. Ashraf, M, Hasnain, S, Berge, O, Mahmood, T. Inoculating wheat seedlings with exopolysaccharide-producing bacteria restricts sodium uptake and stimulates plant growth under salt stress. Biology and Fertility of Soils. 2004; 40:157-162.

75. Jha, A, Saxena, J, Sharma, V. Investigation on Phosphate Solubilization Potential of Agricultural Soil Bacteria as Affected by Different Phosphorus Sources, Temperature, Salt, and pH. Communications in Soil Science and Plant Analysis. 2013; 44:2443-2458.

76. Kasim, WA, Osman, ME, Omar, MN, Abd El-Daim, IA, Bejai, S, Meijer, J. Control of drought stress in wheat using plant-growth-promoting bacteria. Journal of Plant Growth Regulation. 2013; 32:122-130.

77. Alvarez, M, Sueldo, R, Barassi, C. Effect of Azospirillum on coleoptile growth in wheat seedlings under water stress. Cereal Research Communications. 1996; 101-107.

78. Creus, CM, Sueldo, RJ, Barassi, CA. Water relations and yield in Azospirillum-inoculated wheat exposed to drought in the field. Canadian Journal of Botany. 2004; 82:273-281.

79. Turan, M, Gulluce, M, Åžahin, F. Effects of plant-growth-promoting rhizobacteria on yield, growth, and some physiological characteristics of wheat and barley plants. Communications in Soil Science and Plant Analysis. 2012; 43:1658-1673.

80. Arzanesh, MH, Alikhani, H, Khavazi, K, Rahimian, H, Miransari, M. Wheat (Triticum aestivum L.) growth enhancement by Azospirillum sp. under drought stress. World Journal of Microbiology and Biotechnology. 2011; 27:197-205.

81. Verma, P, Yadav, AN, Khannam, KS, Kumar, S, Saxena, AK, Suman, A. Molecular diversity and multifarious plant growth promoting attributes of Bacilli associated with wheat (Triticum aestivum L.) rhizosphere from six diverse agro-ecological zones of India. Journal of Basic Microbiology. 2016; 56:44-58.

82. Verma, P, Yadav, AN, Shukla, L, Saxena, AK, Suman, A. Alleviation of cold stress in wheat seedlings by Bacillus amyloliquefaciens IARI-HHS2-30, an endophytic psychrotolerant K-solubilizing bacterium from NW Indian Himalayas. National Journal of Life Sciences. 2015; 12:105-110.

83. Singh, RP, Jha, PN. A halotolerant bacterium Bacillus licheniformis HSW-16 augments induced systemic tolerance to salt stress in wheat plant (Triticum aestivum). Frontiers in Plant Science. 2016; 7:1890.

84. Chakraborty, U, Chakraborty, B, Chakraborty, A, Dey, P. Water stress amelioration and plant growth promotion in wheat plants by osmotic stress tolerant bacteria. World Journal of Microbiology and Biotechnology. 2013; 29:789.

85. Naveed, M, Hussain, MB, Zahir, ZA, Mitter, B, Sessitsch, A. Drought stress amelioration in wheat through inoculation with Burkholderia phytofirmans strain PsJN. Plant Growth Regulation. 2014; 73:121.

86. Sezen, A, Ozdal, M, Koc, K, Algur, OF. Isolation and Characterization of Plant Growth Promoting Rhizobacteria (PGPR) and Their Effects on Improving Growth of Wheat. Journal of Applied Biological Sciences. 2016; 10.

87. Rana, KL, Kour, D, Verma, P, Yadav, AN, Kumar, V, Singh, DH. Diversity and biotechnological applications of endophytic microbes associated with maize (Zea mays L.) growing in Indian Himalayan regions. In: Proceeding of National Conference on Advances in Food Science and Technology. 2017.

88. El-Azeem, SAA, Mehana, TA, Shabayek, AA. Effect of Seed Inoculation with Plant Growth-Promoting Rhizobacteria on the Growth and Yield of Wheat (Triticum aestivum L.) Cultivated in a Sandy Soil. In: proceedings of the third international conference on future trends in genetics and Biotechnology for safe environment, 2008. 3 (2):69 - 74

89. Chen, C, Xin, K, Liu, H, Cheng, J, Shen, X, Wang, Y, Zhang, L. Pantoea alhagi, a novel endophytic bacterium with ability to improve growth and drought tolerance in wheat. Scientific Reports. 2017; 7: 41564.

90. Yaghoubian, Y, Goltapeh, EM, Pirdashti, H, Esfandiari, E, Feiziasl, V, Dolatabadi, HK, Varma, A, Hassim, MH. Effect of Glomus mosseae and Piriformospora indica on growth and antioxidant defense responses of wheat plants under drought stress. Agricultural Research. 2014; 3:239-245.

91. Abbaspoor, A, Zabihi, HR, Movafegh, S, Asl, MA. The efficiency of plant growth promoting rhizobacteria (PGPR) on yield and yield components of two varieties of wheat in salinity condition. American-Eurasian Journal of Sustainable Agriculture. 2009; 3:824-828

92. Selvakumar, G, Joshi, P, Suyal, P, Mishra, PK, Joshi, GK, Bisht, JK, Bhatt, JC, Gupta, HS. Pseudomonas lurida M2RH3 (MTCC 9245), a psychrotolerant bacterium from the Uttarakhand Himalayas, solubilizes phosphate and promotes wheat seedling growth. World Journal of Microbiology and Biotechnology. 2011; 27:1129-1135.

93. Ali, SZ, Sandhya, V, Grover, M, Linga, VR, Bandi, V. Effect of inoculation with a thermotolerant plant growth promoting Pseudomonas putida strain AKMP7 on growth of wheat (Triticum spp.) under heat stress. Journal of Plant Interactions. 2011; 6:239-246.

94. Mishra, PK, Mishra, S, Bisht, SC, Selvakumar, G, Kundu, S, Bisht, J, Gupta, HS. Isolation, molecular characterization and growth-promotion activities of a cold tolerant bacterium Pseudomonas sp. NARs9 (MTCC9002) from the Indian Himalayas. Biological Research. 2009; 42:305-313.

95. Kumar, V, Singh, P, Jorquera, MA, Sangwan, P, Kumar, P, Verma, A, Agrawal, S. Isolation of phytase-producing bacteria from Himalayan soils and their effect on growth and phosphorus uptake of Indian mustard (Brassica juncea). World Journal of Microbiology and Biotechnology. 2013; 29:1361-1369.

96. Kaur, R, Saxena, A, Sangwan, P, Yadav, AN, Kumar, V, Dhaliwal, HS. Production and characterization of a neutral phytase of Penicillium oxalicum EUFR-3 isolated from Himalayan region. Nusantara Bioscience. 2017; 9:68-76.

97. Li, M, Osaki, M, Rao, IM, Tadano, T. Secretion of phytase from the roots of several plant species under phosphorus-deficient conditions. Plant and Soil. 1997; 195:161-169.

98. Kumar, V, Singh, G, Verma, A, Agrawal, S. In Silico characterization of histidine acid phytase sequences. Enzyme Research. 2012; 2012.

99. Kumar, V, Singh, D, Sangwan, P, Gill, PK. Management of environmental phosphorus pollution using phytases: current challenges and future prospects. In: Applied Environmental Biotechnology: Present Scenario and Future Trends, Springer, 2015; pp. 97-114.

100. Singh, P, Kumar, V, Agrawal, S. Evaluation of phytase producing bacteria for their plant growth promoting activities. International Journal of Microbiology. 2014;

101. Kumar, V, Sangwan, P, Verma, A, Agrawal, S. Molecular and biochemical characteristics of recombinant β-propeller Phytase from Bacillus licheniformis strain PB-13 with potential application in aquafeed. Applied Biochemistry and Biotechnology. 2014; 173:646-659.

102. Huang, H, Shao, N, Wang, Y, Luo, H, Yang, P, Zhou, Z, Zhan, Z, Yao, B. A novel beta-propeller phytase from Pedobacter nyackensis MJ11 CGMCC 2503 with potential as an aquatic feed additive. Applied Microbiology and Biotechnology. 2009; 83:249-259.

103. Lottmann, J, Heuer, H, de Vries, J, Mahn, A, Düring, K, Wackernagel, W, Smalla, K, Berg, G. Establishment of introduced antagonistic bacteria in the rhizosphere of transgenic potatoes and their effect on the bacterial community. FEMS Microbiology Ecology. 2000; 33:41-49.

104. Yadav, AN, Sachan, SG, Verma, P, Kaushik, R, Saxena, AK. Cold active hydrolytic enzymes production by psychrotrophic Bacilli isolated from three sub-glacial lakes of NW Indian Himalayas. Journal of Basic Microbiology. 2016; 56:294-307.

105. Yadav, AN, Verma, P, Kumar, R, Kumar, V, Kumar, K. Current applications and future prospects of eco-friendly microbes. EU Voice. 2017; 3:1-3

106. Kour, D, Rana, KL, Verma, P, Yadav, AN, Kumar, V, Singh, DH. Biofertilizers: Eco-friendly Technologies and Bioresources for Sustainable Agriculture. In: Proceeding of International Conference on Innovative Research in Engineering Science and Technology. 2017; pp.

107. Penella, JS, Collar, C, Haros, M. Effect of wheat bran and enzyme addition on dough functional performance and phytic acid levels in bread. Journal of Cereal Science. 2008; 48:715-721.

108. Hurrell, RF, Reddy, MB, Juillerat, M-A, Cook, JD. Degradation of phytic acid in cereal porridges improves iron absorption by human subjects. The American Journal of Clinical Nutrition. 2003; 77:1213-1219.

109. Jin, F, Frohman, C, Thannhauser, TW, Welch, RM, Glahn, RP. Effects of ascorbic acid, phytic acid and tannic acid on iron bioavailability from reconstituted ferritin measured by an in vitro digestion-Caco-2 cell model. British Journal of Nutrition. 2008; 101:972-981.

110. Frontela, C, Scarino, ML, Ferruzza, S, Ros, G, Martínez, C. Effect of dephytinization on bioavailability of iron, calcium and zinc from infant cereals assessed in the Caco-2 cell model. World Journal of Gastroenterology. 2009; 15:1977-1984.

111. Park, YJ, Park, J, Park, KH, Oh, BC, Auh, JH. Supplementation of Alkaline Phytase (Ds11) in Whole Wheat Bread Reduces Phytate Content and Improves Mineral Solubility. Journal of Food Science. 2011; 76:C791-C794.

112. Sanz-Penella, JM, Laparra, JMs, Sanz, Y, Haros, M. Assessment of iron bioavailability in whole wheat bread by addition of phytase-producing bifidobacteria. Journal of Agricultural and Food Chemistry. 2012; 60:3190-3195.

113. Kumar, V, Yadav, AN, Verema, P, Sangwan, P, Abhishake, S, Singh, B. β-Propeller phytases: Diversity, catalytic attributes, current developments and potential biotechnological applications. International Journal of Biological Macromolecules. 2017; 98:595-609.

114. Phillippy, BQ, Graf, E. Antioxidant functions of inositol 1, 2, 3-trisphosphate and inositol 1, 2, 3, 6-tetrakisphosphate. Free Radical Biology and Medicine. 1997; 22:939-946.

115. Siren, M. Method of treating pain using inositol triphosphate. Google Patents. 1995.

116. Vucenik, I, Shamsuddin, AM. Cancer inhibition by inositol hexaphosphate (IP6) and inositol: from laboratory to clinic. The Journal of Nutrition. 2003; 133:3778S-3784S.

117. Saxena, AK, Yadav, AN, Kaushik, R, Tyagi, S, Kumar, M, Prasanna, R, Shukla, L. Use of Microbes from extreme environments for the benefits of agriculture. In Afro-Asian Congress on microbes for human & environmental health. 2014.

118. Saxena, AK, Yadav, AN, Kaushik, R, Tyagi, SP, Shukla, L. Biotechnological applications of microbes isolated from cold environments in agriculture and allied sectors. In International Conference on “Low Temperature Science and Biotechnological Advances”. Society of low temperature biology, 2015; pp. 104.

119. Kandylis, P, Pissaridi, K, Bekatorou, A, Kanellaki, M, Koutinas, AA. Dairy and non-dairy probiotic beverages. Current Opinion in Food Science. 2016; 7:58-63.

120. Holzapfel, W. Appropriate starter culture technologies for small-scale fermentation in developing countries. International Journal of Food Microbiology. 2002; 75:197-212.

121. Konings, WN, Kok, J, Kuipers, OP, Poolman, B. Lactic acid bacteria: the bugs of the new millennium. Current Opinion in Microbiology. 2000; 3:276-282.

122. Adams, M. Safety of industrial lactic acid bacteria. Journal of Biotechnology. 1999; 68:171-178.

123. Lee, I-C, Caggianiello, G, van Swam, II, Taverne, N, Meijerink, M, Bron, PA, Spano, G, Kleerebezem, M. Strain-specific features of extracellular polysaccharides and their impact on Lactobacillus plantarum-host interactions. Applied and Environmental Microbiology. 2016; 82:3959-3970.

124. Vlasova, AN, Kandasamy, S, Chattha, KS, Rajashekara, G, Saif, LJ. Comparison of probiotic Lactobacilli and Bifidobacteria effects, immune responses and rotavirus vaccines and infection in different host species. Veterinary Immunology and Immunopathology. 2016; 172:72-84.

125. McFarland, LV, Malfertheiner, P, Huang, Y, Wang, L. Meta-analysis of single strain probiotics for the eradication of Helicobacter pylori and prevention of adverse events. World Journal of Meta-analysis. 2015; 3:97-117.

126. Prescott, SL, Björkstén, B. Probiotics for the prevention or treatment of allergic diseases. Journal of Allergy and Clinical Immunology. 2007; 120:255-262.

127. Albano, H, van Reenen, CA, Todorov, SD, Cruz, D, Fraga, L, Hogg, T, Dicks, LM, Teixeira, P. Phenotypic and genetic heterogeneity of lactic acid bacteria isolated from “Alheira”, a traditional fermented sausage produced in Portugal. Meat Science. 2009; 82:389-398.

128. Chettri, R, Tamang, JP. Bacillus species isolated from tungrymbai and bekang, naturally fermented soybean foods of India. International Journal of Food Microbiology. 2015; 197:72-76.

129. Parente, E, Cogan, T. Starter cultures: general aspects. In: Cheese: chemistry, physics and microbiology. 2004; 1:123-147.

130. Tamang, J, Dewan, S, Thapa, S, Olasupo, N, Schillinger, U, Wijaya, A, Holzapfel, W. Identification and enzymatic profiles of the predominant lactic acid bacteria isolated from soft variety Chhurpi, a traditional cheese typical of the Sikkim Himalayas. Food Biotechnology. 2000; 14:99-112.

131. Hong, S-B, Kim, D-H, Lee, M, Baek, S-Y, Kwon, S-w, Houbraken, J, Samson, RA. Zygomycota associated with traditional meju, a fermented soybean starting material for soy sauce and soybean paste. Journal of Microbiology. 2012; 50:386-393.

132. Shangpliang, H, Sharma, S, Rai, R, Tamang, JP. Some Technological Properties of Lactic Acid Bacteria Isolated from Dahi and Datshi, Naturally Fermented Milk Products of Bhutan. Frontiers in Microbiology. 2017; 8:116.

133. Nguyen, DTL, Van Hoorde, K, Cnockaert, M, De Brandt, E, Aerts, M, Vandamme, P. A description of the lactic acid bacteria microbiota associated with the production of traditional fermented vegetables in Vietnam. International Journal Of Food Microbiology. 2013; 163:19-27.

134. Phan, YTN, Tang, MT, Tran, TTM, Nguyen, VH, Nguyen, TH, Tsuruta, T, Nishino, N. Diversity of lactic acid bacteria in vegetable-based and meat-based fermented foods produced in the central region of Vietnam. AIMS Microbiology. 2017; 3(1):61-70.

135. Oyewole, OB. Lactic fermented foods in Africa and their benefits. Food Control. 1997; 8:289-297.

136. Chen, Ys, Wu, Hc, Lo, Hy, Lin, Wc, Hsu, Wh, Lin, Cw, Lin, Py, Yanagida, F. Isolation and characterisation of lactic acid bacteria from jiang-gua (fermented cucumbers), a traditional fermented food in Taiwan. Journal of the Science of Food and Agriculture. 2012; 92:2069-2075.

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