HYDROLYTIC ENZYME PRODUCING ACTINOMYCETES FROM THE ALKALINE LONAR CRATER ECOSYSTEM AND THEIR BIOTECHNOLOGICAL POTENTIAL
Keywords:
Actinomycetes, Lonar Crater, Hydrolytic Enzymes, Protease, Amylase, Cellulase, LipaseAbstract
Actinomycetes are well known for their ability to produce a wide range of extracellular enzymes and therefore represent an important source of industrially useful biocatalysts. In the present study, actinomycetes isolated from the extreme environmental conditions of Lonar Crater, Maharashtra, India, were investigated for their ability to produce hydrolytic enzymes. Isolates recovered from water, sediment, and microbial mat samples were screened qualitatively for four extracellular enzymes, namely protease, amylase, cellulase, and lipase as these are the main hydrolytic enzymes. The isolates showed noticeable differences in their enzyme-producing profiles. The isolates were tentatively identified in the analysis based on morphological, physiological, biochemical and cultural characteristics. Nocardiopsis synnemataformans was positive for protease, amylase, and cellulase production but did not exhibit lipase activity. In contrast, Streptomyces viridodiastaticus produced protease, amylase, and lipase, while cellulase activity was not detected. Among the tested isolates, Nocardiopsis valiformis and Nocardiopsis alba showed positive reactions for all four enzymes. These findings indicate that actinomycetes inhabiting the Lonar Crater ecosystem possess varied hydrolytic capabilities, which may be associated with their adaptation to the physicochemical conditions of this unusual environment. The enzyme-positive isolates, particularly those exhibiting multiple activities, could serve as promising candidates for further studies involving enzyme production, optimization of culture conditions, purification, characterization, and assessment of potential industrial applications.
References
I. Bharathi, D., & Rajalakshmi, G. (2019). Microbial lipases: An overview of screening, production and purification. Biocatalysis and Agricultural Biotechnology, 22, 101368.
II. Beeson, W. T., Vu, V. V., Span, E. A., Phillips, C. M., & Marletta, M. A. (2015). Cellulose degradation by polysaccharide monooxygenases. Annual Review of Biochemistry, 84, 923–946.
III. Dastager, S. G., Mawlankar, R. S., Mual, P., Verma, A., Krishnamurthy, Y. L., & Dharne, M. S. (2016). Streptomyces lonarensis sp. nov., isolated from Lonar Lake, a meteorite salt water lake in India. International Journal of Systematic and Evolutionary Microbiology, 66, 1036–1042.
IV. Laxman, R. S., & Srinivasan, M. C. (1993). Actinomycetes as resource pools for industrially useful enzymes: An overview. Hindustan Antibiotics Bulletin, 35(1–2), 23–32.
V. Mukhtar, S., Zaheer, A., Aiysha, D., Malik, K. A., & Mehnaz, S. (2017). Actinomycetes: A source of industrially important enzymes. Journal of Proteomics & Bioinformatics, 10(12).
VI. Saini, A., Aggarwal, N. K., Sharma, A., & Yadav, A. (2015). Actinomycetes: A source of lignocellulolytic enzymes. Enzyme Research, 2015, 279381.
VII. Sathya, R., Ushadevi, T., & others. (2013). Actinomycetes: A repertory of green catalysts with a potential revenue resource. BioMed Research International, 2013, Article 204961.
VIII. Singh, S. P., et al. (2015). Thermophilic and alkaliphilic Actinobacteria: Biology and potential applications. Frontiers in Microbiology, 6, 1014.
IX. Suriya, J., Bharathiraja, S., Manivasagan, P., & Kim, S.-K. (2016). Enzymes from rare actinobacterial strains. Advances in Food and Nutrition Research, 79, 67–98.
X. Wang, Y., et al. (1988). Production of exogenous lipases by bacteria, fungi, and actinomycetes. Enzyme and Microbial Technology, 10(8), 492–497.
XI. Raut, M. P., et al. (2013). Microbiology of Lonar Lake and other soda lakes. The ISME Journal, 7, 468–476.
XII. Suman, V., Leena, T., & Yugandhar, N. M. (2020). A review: A source of industrially important enzymes from marine actinomycetes. Research & Reviews: A Journal of Biotechnology.
XIII. Production strategies and biotechnological relevance of microbial lipases: A review. (2021). Microbial Cell Factories.
XIV. Actinobacteria: Diversity and biotechnological applications. (2018). In New and future developments in microbial biotechnology and bioengineering (pp. 165–177). Elsevier.
XV. Joshi, A. A., Kanekar, P. P., Kelkar, A. S., Shouche, Y. S., Vani, A. A., Borgave, S. S., & Sarnaik, S. S. (2008). Cultivable bacterial diversity of alkaline Lonar lake, India. Microbial Ecology, 55(2), 163–172.
XVI. Kumbhare, S. V., Mhatre, S. S., Chowdhury, S. P., Shetty, S. A., Marathe, N. P., Bhute, S., & Shouche, Y. S. (2015). Exploration of microbial diversity and community structure of Lonar Lake: The only hypersaline meteorite crater lake within basalt rock. Frontiers in Microbiology, 6, 1553.
XVII. Sharma, T. K., Mawlankar, R., Sonalkar, V. V., Shinde, V. K., Zhan, J., Li, W.-J., Rele, M. V., Dastager, S. G., & Kumar, L. S. (2016). Streptomyces lonarensis sp. nov., isolated from Lonar Lake, a meteorite salt water lake in India. Antonie van Leeuwenhoek, 109, 225–235.
XVIII. Singh, et al. (2024). Industrial and pharmaceutical applications of microbial diversity of hypersaline ecology from Lonar Soda Crater. [Use the exact author list and journal details from the paper before adding this to your final reference list.]
XIX. Goodfellow, M., & Williams, S. T. (1983). Ecology of actinomycetes. Annual Review of Microbiology, 37, 189–216. https://doi.org/10.1146/annurev.mi.37.100183.001201
XX. Hankin, L., & Anagnostakis, S. L. (1975). The use of solid media for detection of enzyme production by fungi and bacteria. Mycologia, 67(3), 597–607.
XXI. George, S. P., Ahmad, A., & Rao, M. B. (2001). Studies on carboxymethyl cellulase produced by an alkaline-tolerant Aspergillus niger in solid-state cultivation. Process Biochemistry, 36(10), 985–992.
XXII. Janda, J. M., & Abbott, S. L. (2007). 16S rRNA gene sequencing for bacterial identification in the diagnostic laboratory: Pluses, perils, and pitfalls. Journal of Clinical Microbiology, 45(9), 2761–2764.
XXIII. Bull, A. T. Asenjo, J. A., Goodfellow, M. and Gómez-Silva, B. (2016). The Atacama Desert: Technical resources and the growing importance of novel microbial diversity. Annual Review of Microbiology, 70, 215–234.
XXIV. Kanekar P.P, Joshi A.A, Kelkar AS, Borgave SB and Sarnaik SS, (2008). Alkaline Lonar Lake, India-a treasure of alkaliphilic and halophilic bacteria, In: Proceedings of Taal: The World Lake Conference 12, Eds M. Sengupta and R Dalwani: 1765-1774.
XXV. Dawoud, T. M., Alharbi, N. S., Theruvinthalakal, A. M., Thekkangil, A., Kadaikunnan, S., Khaled, J. M., Almanaa, T. N., Sankar, K., Innasimuthu, G. M., Alanzi, K. F., & Rajaram, S. K. (2020). Characterization and antifungal activity of the yellow pigment produced by a Bacillus sp. DBS4 isolated from the lichen Dirinaria aegialita. Saudi Journal of Biological Sciences, 27(5), 1403–1411.
XXVI. Dhivya, S. M., & Kalaichelvi, K. (2017). UV-visible spectroscopic and FTIR analysis of Sarcostemma brevistigma Wight. & Arn. International Journal of Current Pharmaceutical Research, 9(3), 46–49.
Downloads
Published
How to Cite
Issue
Section
License
Copyright (c) 2026 International Educational Applied Scientific Research Journal

This work is licensed under a Creative Commons Attribution 4.0 International License.