Isolation and in vitro screening of Pink Pigmented Facultative Methylobacterium (PPFMs) isolates for the production of phytohormones and ACC deaminase activity from the tea plantations of South India

Authors

  • S. Marimuthu Parry Agro R&D Center, Parry Agro Industries Limited, Murugalli Estate, Valparai-642 125, Tamil Nadu
  • S. Anitha Parry Agro R&D Center, Parry Agro Industries Limited, Murugalli Estate, Valparai-642 125, Tamil Nadu
  • G. Ragupathi Parry Agro R&D Center, Parry Agro Industries Limited, Murugalli Estate, Valparai-642 125, Tamil Nadu
  • P. Nepolean UPASI Tea Research Foundation, Tea Research Institute, Nirar Dam (BPO), Valparai-642124, Tamil Nadu
  • L. Mendez UPASI Tea Research Foundation, Tea Research Institute, Nirar Dam (BPO), Valparai-642124, Tamil Nadu
  • P. Thangaraj Parry Agro R&D Center, Parry Agro Industries Limited, Murugalli Estate, Valparai-642 125, Tamil Nadu
  • S. Suganthi Parry Agro R&D Center, Parry Agro Industries Limited, Murugalli Estate, Valparai-642 125, Tamil Nadu

DOI:

https://doi.org/10.25081/jpc.2023.v51.i1.8467

Abstract

Pink Pigmented Facultative Methylobacterium (PPFMs) strains were considered as highly efficient growth-promoting bacteria and are ACC deaminase producers which mitigate the drought impact in crop plants. Hence, PPFM strains were isolated from phyllosphere of the tea plantations of south India. A total of 253 bacterial isolates were obtained by using Methanol-AMS medium adopting standard methods. Among the 253 isolates, 105 potential isolates were screened for the production of plant growth hormones viz., IAA, GA3, carotenoids, and 35 potential isolates for ACC deaminase activity. Among 35 isolates tested, 5 isolates viz., MBVPR19D.L23 (51.7 µg/mL), MBANML10H.L06 (45.1 µg/mL), MBVPR19D.L22 (42.0 µg/mL), MBANML10H.L11 (40.5 µg/mL) and MBVPR UPASI L. An H.L13 (40.0 µg/mL) were found to produce higher level of IAA, GA3, and Carotenoids. The highest activity of ACC deaminase was registered in the isolates of Central Travancore namely MBVPR19D.L22 and MBVPR19D.L23 along with one isolate MBKDMVG26H.L37 from Karnataka. The selected strains of MBVPR19 D.L22/23 were identified as Methylobacterium radiotolerans (OL440712) using 16s rRNA molecular technique. This is the first report of isolation of genus Methylobacterium from the acidic environment of tea ecosystem in South India. The present study also suggest that plant growth hormones and ACC deaminase enzyme activity of Methylobacterium species could play a critical role in mitigating the drought stress for a sustainable productivity in tea.

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References

Anitha, K.G. 2010. Enhancing seed germination of mono and Dicotyledons through IAA production of PPFM. Trends in soil & Plant sciences Journal1(1):14-18.

Arshad, M., Shaharoona, B., and Mahmood T. 2008. Inoculation with Pseudomonas spp. containing ACC-deaminase partially eliminates the effects of drought stress on growth, yield, and ripening of pea (Pisum sativum L.). Pedosphere18: 611-620

Bano, A., Hansen, H., Dorffling, .K and Hahn, H. 1994. Changes in the contents of free and conjugated abscisic acid, phaseic acid and cytokinins in xylem sap of drought stressed sunflower plants. Phytochemistry37: 345–347

Bongers, T. and Ferris, H. 1999). Nematode community structure as a bioindicator in environmental monitoring. Trends in Ecology & Evolution 14(6): 224-228.

Bora, S.S., Dey, K.K., Borah, M., Rahman, M., Gogoi, M., Modi, M.K. and Barooah, M. 2021. Niche differentiation of microbes and their functional signatures in Assam type tea (Camellia sinensis var. assamica).Preprint from Research Square, 26 Mar 2021 DOI: 10.21203/rs.3.rs-347764/v1

Cakmakci, R. 2019. The variability of the predominant culturable plant growth promoting Rhizobacterial diversity in the acidic tea rhizosphere soils in the eastern black sea region. Alinteri Journal of Agricultural Science34(2): 175-181.

Chinnadurai, C., Balachandar, D., and Sundaram, S. P. 2009. Characterization of 1-aminocyclopropane-1-carboxylate deaminase producing methylobacteria from phyllosphere of rice and their role in ethylene regulation. World Journal of Microbiology and Biotechnology 25(8): 1403-1411.

Farooq, M., Basra, S. M. A., Wahid, A., Ahmad, N. and Saleem, B. A. 2009. Improving the drought tolerance in rice (Oryza sativa L.) by exogenous application of salicylic acid. Journal of Agronomy and Crop Science195: 237–246

Gentry, A. H. 1988. Changes in plant community diversity and floristic composition on environmental and geographical gradients. Annals of the Missouri botanical garden, 1-34.

Glick, B.R., Cheng, Z., , Czarny, J. and Duan, J. 2007. Promotion of plant growth by ACC deaminase producing soil bacteria. European Journal of Plant Pathology 119: 329-339

Gomez, K.A. and Gomez, A.A. 1984. Statistical Procedures for Agricultural Research. 2nd Edition, John Wiley and Sons, New York, 680 p.

Gordon, S.A. and Weber, R.P. 1951. A method for estimation of Indole acetic acid. Plant Physiol. 26: 192-195.

Honma, M. and Shimomura, T. 1978. Metabolism of 1-aminocyclopropane-1-carboxylic acid. Agricultural and

Biological Chemistry, 42(10), pp.1825-1831.

Kang, B.G., Kim W.T., Yun H.S. and Chang S.C. 2010. Use of plant growth-promoting rhizobacteria to control stress responses

of plant roots. Plant Biotechnology Reports 4: 179-183 Kumar, M., Kour D., Yadav, A., Saxena R., Rai, P., Jyoti A. and

Tomar R.S. 2019. Biodiversity of Methylotrophic microbial communities and their potential role in mitigation of abiotic stress in plants. Biologia 74 : 287-308.

Lidstrom, M.E. and Chistoserdova, L. 2002. Plants in the cytokinin: cytokinin production by Methylobacterium. J. Bacteriol 184: 1818.

Ma, W., Sebestian S.B., Burd J., Guinel G.I. and Glick B.R. 2003. Prevalence of 1-aminocyclopropane-1-carboxylate

deaminase in Rhizobium spp. Anton. Leeuw 83: 285-291

Mahadevan A, Sridhar R . 1986. Methods in Physiological Plant Pathology. 3 rd Edn. Sivakami Publication, Madras. India p. 316

Manival, L., Marimuthu, S., Venkatesalu, V. and Raj Kumar, R. 1994. Effect of potassium nutrition and growth regulators on photosynthesis and assimilate translocation in tea. In: Proceedings of the International Seminar on Integrated Crop Management in Tea: Towards Higher Productivity, International Potash Institute, Basel, Switzerland, Colombo,

Sri Lanka, pp. 217–223.

Meena, K.K., Sorty, A.M., Bitle, U.M., Chaudhari, K., Gupta, P., Pareek, A., Singh, D.P., Prabha, R., Shu, P.K., Gupta, V. K., Singh, H.P., Krihnani, K. and Minhas, P.S. 2017. Abiotic stress responses and microbe mediated mitigation in plants: The OMIC strategies. Front. Plant Science 8: 1-42.

Nepolean, P., Jayanthi, R., Mareeswaran, J. and Radhakrishnan, B. 2015. Plant Protection Development in Tea Plantations of South India in the Last Five Decades. Journal of Tea Science Research 5 (7): 1-6

Raghavendra J, G.P. Santhosh, Mahadevaswamy,S.Shubha, and M.V.Ravi. 2019. In vitro screening of Pink Pigmented Facultative Methylotrophs based on their functional characteristics. Int. J. Pur . App. Biosci. 7(1):553-562.

Ram Kailash P. Yadav, Katerina Karamanoli and Despoina Vokou,2010, Estimating bacterial population on the Phyllosphere by serial dilution platting and leaf imprint methods,ECOPRINT 17:47-52.

Rivero, R. M., Kojima, M., Gepstein, A., Sakakibara, H., Mittler, R., Gepstein, S. and Blumwald, E. 2007. Delayed leaf senescence induces extreme drought tolerance in a flowering plant. Proc Natl Acad Sci104:19631–19636

Saravanakumar, V., Balasubrmanian, R., Kumaran, S. T., &Venkadesan, K. 2014. Strategies to Mitigate the Impact of Poor Monsoon on Agriculture'. Final Report. State Planning. Commission, Chennai.

Senthilkumar, M. and Krishnamoorthy, R. 2017. Isolation and C h a r a c t e r i z a t i o n o f To m a t o L e a f P h y l l o s p h e r e Methylobacterium and their Effect on Plant Growth Int. J. Curr. Microbiol. App. Sci . 6 (11): 2121-2136.

Shaik Zulfikar Ali, Vardharajula Sandhya, Linga Venkateswar Rao, 2013. Isolation and characterization of drought-tolerant ACC deaminase and exopolysaccharide-producing fluorescent Pseudomonas sp. ICRISAT -Annals of Microbiology:1-10.

Sivakumar, R. D. K., Nandhitha, P., Chadrasekaran, P., Boominathan, P. and Senthilkumar, M. 2017. Impact of Pink Pigmented Facultative Methylotrophs and PGRs on water status, photosynthesis, proline and NR activity tomato under drought. Int. J.Curr.Microbiol.App.Sci. 6(5): 1640-1651

Swaine, M. D., & Becker, P. 1999. Woody life-form composition and association on rainfall and soil fertility gradients in Ghana. Plant Ecology 145(1):167-173.

Webb, C. O., & Peart, D. R. (2000). Habitat associations of trees and seedlings in a Bornean rain forest. Journal of Ecology 88(3): 464-478.

Whittenbury, R., Phillips, K.C. and Wilkinson, J.F. 1970. Enrichment, isolation and some properties of methane-utilizing bacteria. Microbiology 61(2): 205-218.

Xie H., Feng X., Wang M., Wang, Y., Awasthi, M.K. and Xu, P. 2020. Implications of endophytic Microbiota in Camellia sinensis. a review on current understanding and future insights. Bioengineered 11(1): 1001-1015.

Xiaomei Yan, Zhi-Jie Wang, Yu Mei, Ligun Wang, Xu Wang, Qingshan Xu, Su Peng, Yu Zhou, ChaolingWei . 2018. Isolation, Diversity, and Growth-Promoting Activities of Endophytic Bacteria From Tea Cultivars of Zijuan and Yunkang-10. Frontiers in Microbiology 9 : 1- 11.

Zheng, C., Wang, Y., Ding, Z., Zhao, L. 2016. Global transcriptional analysis reveals the complex relationship between tea quality, leaf senescence and the responses to cold-drought combined stress in Camellia sinensis. Front Plant Sci. 7 : 1-19.

Published

20-10-2023

How to Cite

Marimuthu, S., Anitha, S., Ragupathi, G., Nepolean, P., Mendez, L., Thangaraj, P., & Suganthi, S. (2023). Isolation and in vitro screening of Pink Pigmented Facultative Methylobacterium (PPFMs) isolates for the production of phytohormones and ACC deaminase activity from the tea plantations of South India. Journal of Plantation Crops, 51(1), 9–15. https://doi.org/10.25081/jpc.2023.v51.i1.8467

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Research Articles