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Investigating potential protease activity of psychrotrophic bacteria from a municipal landfill for solid waste management

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Abstract

A municipal landfill contains different waste materials that support the growth of a diverse community of enzyme-secreting microorganisms that degrade and detoxify the wastes. The present study aimed to explore psychrotrophic protein-degrading bacteria for converting proteinaceous waste into the nutrient-rich end product of agricultural applications. During the study, twenty five morphologically different psychrotrophic proteolytic bacteria were isolated from the landfill soil samples using standard serial dilution and spread plate techniques. The isolates showed variable protease activities at different incubation temperatures (5 °C, 10 °C, 15 °C, and 20 °C). However, isolate PB2 showed significantly (p < 0.05) highest protease activity (1.53 ± 0.8 1U/mL) at 20 °C with corresponding hydrolysis zone of average diameter of 17 ± 2 mm through primary screening. The isolate (PB2) also exhibited the hydrolysis of several protein substrates, including elastin and gelatin. According to protease inhibition studies, the extracellular proteases released by isolating PB2 were primarily serine and metalloproteases. The morphological, biochemical, and molecular characterization (16S rRNA) demonstrated that the isolate had 99% similarity with Pseudomonas fluorescens strain SU003 (NCBI, Accession No. MH266220). The results indicated that psychrotrophic bacteria isolated from the temperate landfill site displayed promising protease activities at lower temperatures and can be utilized for converting voluminous organic wastes generated in Himalayan regions via cold composting to produce nutrient-rich compost of agricultural importance.

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Abbreviations

ANOVA:

One-way analysis of variance

DMRT:

Duncan’s multiple range test

IU:

International units

MSW:

Municipal solid waste

NCBI:

National Center for Biotechnology Information

OP:

1,10-Phenanthroline

PCR:

Polymerase chain reaction

PMSF:

Phenylmethylsulfonyl fluoride

TCA:

Trichloroacetic acid

References

  1. Juarez MB, Mondelli G, Giacheti HL (2023) An overview of in situ testing and geophysical methods to investigate municipal solid waste landfills. Environ Sci Pollut Res 1–11. https://doi.org/10.1007/s11356-023-25203-5

  2. Michalska J, Piński A, Żur J, Mrozik A (2020) Selecting bacteria candidates for the bioaugmentation of activated sludge to improve the aerobic treatment of landfill leachate. Water 12:140. https://doi.org/10.3390/w12010140

    Article  Google Scholar 

  3. Hamid B, Yatoo AM, Jehangir A, Baba ZA, Tyub S, Bhat SA, Ameen F (2022) Characterization and efficiency evaluation of cold active bacterial isolates for treatment of sanitary landfill leachate. Int J Environ Sci 16:65. https://doi.org/10.1007/s41742-022-00441-6

    Article  Google Scholar 

  4. Sekhohola-Dlamini L, Tekere M (2020) Microbiology of municipal solid waste landfills: a review of microbial dynamics and ecological influences in waste bioprocessing. Biodegradation 31:1–21. https://doi.org/10.1007/s10532-019-09890-x

    Article  Google Scholar 

  5. Masi C, Tebiso A, Kumar KS (2023) Isolation and characterization of potential multiple extracellular enzyme-producing bacteria from waste dumping area in Addis Ababa. Heliyon 9:1–14. https://doi.org/10.1016/j.heliyon.2022.e12645

    Article  Google Scholar 

  6. Ali M, Yue D (2020) Population dynamics of microbial species under high and low ammonia nitrogen in the alternate layer bioreactor landfill (ALBL) approach. Bioresour Technol 315:123787. https://doi.org/10.1016/j.biortech.2020.123787

    Article  Google Scholar 

  7. Mishra S, Lin Z, Pang S, Zhang W, Bhatt P, Chen S (2021) Recent advanced technologies for the characterization of xenobiotic-degrading microorganisms and microbial communities. Front Bioeng Biotechno 9:632059. https://doi.org/10.3389/fbioe.2021.632059

    Article  Google Scholar 

  8. Munawar A, Shaheen M, Ramzan S, Masih SA, Jabeen F, Younis T, Aslam M (2023) Diversity and enzymatic potential of indigenous bacteria from unexplored contaminated soils in Faisalabad. Heliyon 9:1–15. https://doi.org/10.1016/j.heliyon.2023.e15256

    Article  Google Scholar 

  9. Song C, Zhang Y, Xia X, Qi H, Li M, Pan H, Xi B (2018) Effect of inoculation with a microbial consortium that degrades organic acids on the composting efficiency of food waste. Microb Biotechnol 11:1124–1136. https://doi.org/10.1111/1751-7915.13294

    Article  Google Scholar 

  10. Hamid B (2020) Decomposition of solid waste and landfill leachate under temperate conditions. Thesis. University of Kashmir, India

    Google Scholar 

  11. Mushtaq H, Ganai SA, Jehangir A, Ganai BA, Dar R (2023) Molecular and functional characterization of protease from psychrotrophic Bacillus sp. HM49 in North-Western Himalaya. PLoS ONE 18:1–24. https://doi.org/10.1371/journal.pone.0283677

    Article  Google Scholar 

  12. Hamid B, Jehangir A, Baba ZA, Fatima S (2019) Isolation and characterization of cold active bacteria from municipal solid waste landfill site. Res J Environ Sci 13:1–9. https://doi.org/10.3923/rjes.2019.1.9

    Article  Google Scholar 

  13. Matkawala F, Nighojkar S, Kumar A, Nighojkar A (2021) Microbial alkaline serine proteases: production, properties, and applications. World J Microbiol Biotechnol 37:1–12. https://doi.org/10.1007/s11274-021-03036-z

    Article  Google Scholar 

  14. Jagadeesan Y, Meenakshisundaram S, Saravanan V, Balaiah A (2022) Greener and sustainable biovalorization of poultry waste into peptone via Bacto-enzymatic digestion: a breakthrough chemical-free bioeconomy waste management approach. Waste Biomass Valorization 13:3197–3219. https://doi.org/10.1007/s12649-022-01713-0

    Article  Google Scholar 

  15. Ashraf M, Hussain N, Baqar Z, Kumar A, Ferreira LFR, Iqbal HM (2023) Bioprospecting microbial proteases in various industries/sectors. In: Microbial Biomolecules. Academic Press, pp 301–324

  16. Dhayalan A, Velramar B, Govindasamy B, Ramalingam KR, Dilipkumar A, Pachiappan P (2022) Isolation of a bacterial strain from the gut of the fish, Systomus sarana, identification of the isolated strain, optimized production of its protease, the enzyme purification, and partial structural characterization. J Genet Eng Biotechnol 20:1–15. https://doi.org/10.1186/s43141-022-00299-3

    Article  Google Scholar 

  17. Gurumallesh P, Alagu K, Ramakrishnan B, Muthusamy S (2019) A systematic reconsideration on proteases. Int J Biol Macromol 128:254–267. https://doi.org/10.1016/j.ijbiomac.2019.01.081

    Article  Google Scholar 

  18. Guleria S, Walia A, Chauhan A, Shirkot CK (2016) Molecular characterization of alkaline protease of Bacillus amyloliquefaciens SP1 involved in biocontrol of Fusarium oxysporum. Int J Food Microbiol 232:134–143. https://doi.org/10.1016/j.ijfoodmicro.2016.05.030

    Article  Google Scholar 

  19. Akram Z, Asgher M, Qamar SA (2023) Microbial proteases—robust biocatalytic tools for greener biotechnology. In: Kumar A, Bilal M, Ferreira LFM, Kumari M (eds) Developments in applied microbiology and biotechnology, microbial biomolecules. Academic press, pp 405–427. https://doi.org/10.1016/B978-0-323-99476-7.00004-1

  20. Baba ZA, Hamid B, Sheikh TA et al (2021) Psychrotolerant mesorhizobium sp. isolated from temperate and cold desert regions solubilizes potassium and produces multiple plant growth-promoting metabolites. Molecules 26:1–24. https://doi.org/10.3390/molecules26195758

    Article  Google Scholar 

  21. Hamid B, Zaman M, Farooq S, Fatima S, Sayyed RZ, Baba ZA, Suriani NL (2021) Bacterial plant biostimulants: a sustainable way towards improving growth, productivity, and health of crops. Sustainability 13:1–24. https://doi.org/10.3390/su13052856

    Article  Google Scholar 

  22. Liya SM, Umesh M, Nag A, Chinnathambi A, Alharbi SA, Jhanani GK, Brindhadevi K (2023) Optimized production of keratinolytic proteases from Bacillus tropicus LS27 and its application as a sustainable alternative for dehairing, destaining and metal recovery. Environ Res 115283. https://doi.org/10.1016/j.envres.2023.115283

  23. Annapure US, Pratisha N (2022) Psychrozymes: a novel and promising resource for industrial applications. In: Kuddus M (ed) Microbial extremozymes. Academic press, pp 185–195. https://doi.org/10.1016/B978-0-12-822945-3.00018-X

  24. Furhan J, Salaria N, Jabeen M, Qadri J (2019) Partial purification and characterization of cold-active metalloprotease by Bacillus sp. AP1 from Apharwat Peak, Kashmir. Pakistan J Biotechnol 16:47–54. https://doi.org/10.34016/pjbt.2019.16.1.8

  25. Zhang DC, Brouchkov A, Griva G, Schinner F, Margesin R (2013) Isolation and characterization of bacteria from ancient Siberian permafrost sediment. Biology 2:85–106. https://doi.org/10.3390/biology2010085

    Article  Google Scholar 

  26. Yadav AN, Sachan SG, Verma P, Kaushik R, Saxena AK (2016) Cold active hydrolytic enzymes production by psychrotrophic Bacilli isolated from three sub-glacial lakes of NW Indian Himalayas. J Basic Microbiol 56:294–307. https://doi.org/10.1002/jobm.201500230

    Article  Google Scholar 

  27. Zhou C, Qin H, Chen X, Zhang Y, Xue Y, Ma Y (2018) A novel alkaline protease from alkaliphilic Idiomarina sp. C9–1 with potential application for eco-friendly enzymatic dehairing in the leather industry. Sci Rep 8:16467. https://doi.org/10.1038/s41598-018-34416-5

  28. Lowry OH, Rosebrough NJ, Far AL, Randall RJ (1951) Protein measurement with Folin phenol reagent. J Biol Chem 193:265–275

    Article  Google Scholar 

  29. Zhou MY, Chen XL, Zhao HL, Dang HY, Luan XW, Zhang XY, Zhang YZ (2009) Diversity of both the cultivable protease-producing bacteria and their extracellular proteases in the sediments of the South China Sea. Microb Ecol 58:582–590. https://doi.org/10.1007/s00248-009-9506-z

    Article  Google Scholar 

  30. Buchanan RE, Gibbons NE (1974) Bergey’s manual of determinative bacteriology, 8th edn. Williams and Wilkins, Baltimore, p 1268

  31. Perfumo A, Freiherr von Sass GJ, Nordmann EL, Budisa N, Wagner D (2020) Discovery and characterization of a new cold-active protease from an extremophilic bacterium via comparative genome analysis and in vitro expression. Front Microbiol 11:881. https://doi.org/10.3389/fmicb.2020.00881

    Article  Google Scholar 

  32. Saitou N, Nei M (1987) The neighbor-joining method: a new method for reconstructing phylogenetic trees. Mol Biol Evol 4:406–425. https://doi.org/10.1093/oxfordjournals.molbev.a040454

    Article  Google Scholar 

  33. Kimura M (1980) A simple method for estimating evolutionary rates of base substitutions through comparative studies of nucleotide sequences. J Mol Evol 16:111–120. https://doi.org/10.1007/BF01731581

    Article  Google Scholar 

  34. Kumar S, Stecher G, Li M, Knyaz C, Tamura K (2018) MEGA X: molecular evolutionary genetics analysis across computing platforms. Mol Biol Evol 35:1547. https://doi.org/10.1093/molbev/msy096

    Article  Google Scholar 

  35. Deng C, Zhao R, Qiu Z, Li B, Zhang T, Guo F, Yu K (2022) Genome-centric metagenomics provides new insights into the microbial community and metabolic potential of landfill leachate microbiota. Sci Total Environ 816:151635. https://doi.org/10.1016/j.scitotenv.2021.151635

    Article  Google Scholar 

  36. Hou N, Wen L, Cao H, Liu K, An X, Li D, Li C (2017) Role of psychrotrophic bacteria in organic domestic waste composting in cold regions of China. Bioresour Technol 236:20–28. https://doi.org/10.1016/j.biortech.2017.03.166

    Article  Google Scholar 

  37. Angelin J, Kavitha M (2022) Molecular mechanisms behind the cold and hot adaptation in extremozymes. In: Extremozymes and their industrial applications. Academic Press, pp 141–176

  38. Raj A, Khess N, Pujari N, Bhattacharya S, Das A, Rajan SS (2012) Enhancement of protease production by Pseudomonas aeruginosa isolated from dairy effluent sludge and determination of its fibrinolytic potential. Asian Pac J Trop Biomed 2:S1845–S1851. https://doi.org/10.1016/S2221-1691(12)60506-1

    Article  Google Scholar 

  39. Souza TSPD, de Andrade CJ, Koblitz MGB, Fai AEC (2023) Microbial peptidase in food processing: current state of the art and future trends. Catal Lett 153:114–137. https://doi.org/10.1007/s10562-022-03965-w

    Article  Google Scholar 

  40. Rao R, Vimudha M, Kamini NR, Gowthaman MK, Chandrasekran B, Saravanan P (2017) Alkaline protease production from Brevibacterium luteolum (MTCC 5982) under solid-state fermentation and its application for sulfide-free un-hairing of cowhides. Appl Biochem Biotechnol 182:511–528. https://doi.org/10.1007/s12010-016-2341-z

    Article  Google Scholar 

  41. Yang Z, Huang Z, Wu Q, Tang X, Huang Z (2023) Cold-adapted proteases: an efficient and energy-saving biocatalyst. Int J Mol Sci 24:8532. https://doi.org/10.3390/ijms24108532

    Article  Google Scholar 

  42. Hashmi S, Iqbal S, Ahmed I, Janjua HA (2022) Production, optimization, and partial purification of alkali-thermotolerant proteases from newly isolated Bacillus subtilis S1 and Bacillus amyloliquefaciens KSM12. Processes 10:1050. https://doi.org/10.3390/pr10061050

    Article  Google Scholar 

  43. Salwan R, Sharma V, Kasana RC, Gulati A (2020) Bioprospecting psychrotrophic bacteria for serine-type proteases from the cold areas of Western Himalayas. Curr Microbiol 77:795–806. https://doi.org/10.1007/s00284-020-01876-w

    Article  Google Scholar 

  44. Fuka MM, Engel M, Gattinger A, Bausenwein U, Sommer M, Munch JC, Schloter M (2008) Factors influencing variability of proteolytic genes and activities in arable soils. Soil Biol Biochem 40:1646–1653. https://doi.org/10.1016/j.soilbio.2008.01.028

    Article  Google Scholar 

  45. Leng W, Wu X, Qi X, Liu H, Yuan L, Gao R (2023) Systematic functional analysis and potential application of a serine protease from cold-adapted Planococcus bacterium. Food Sci Hum Wellness 12:1751–1761. https://doi.org/10.1016/j.fshw.2023.02.025

    Article  Google Scholar 

  46. Wang Y, Sun J, Deng Y, Tu Y, Niu H, Cai W, Han X (2022) Whey protein influences the production and activity of extracellular protease from Pseudomonas fluorescens W3. LWT 154:112865. https://doi.org/10.1016/j.lwt.2021.112865

    Article  Google Scholar 

  47. Wang J, Xu A, Wan Y, Li Q (2013) Purification and characterization of a new metallo-neutral protease for beer brewing from Bacillus amyloliquefaciens SYB-001. Appl Biochem Biotechnol 170:2021–2033. https://doi.org/10.1007/s12010-013-0350-8

    Article  Google Scholar 

  48. Furhan J, Nissar J (2021) Cold-adapted serine metalloprotease from Serratia DLCP2: purification, characterization and industrial potential. Appl Biochem 57:40–47. https://doi.org/10.1134/S0003683821010087

    Article  Google Scholar 

  49. Pandey A, Jain R, Sharma A, Dhakar K, Kairam GS, Rahi P, Shouche YS (2019) 16S rRNA gene sequencing and MALDI-TOF mass spectrometry based comparative assessment and bioprospection of Psychrotolerant bacteria isolated from high altitudes under mountain ecosystem. SN Appl Sci 1:1–12. https://doi.org/10.1007/s42452-019-0273-2

    Article  Google Scholar 

  50. Farooq S, Nazir R, Ganai SA, Ganai BA (2021) Isolation and characterization of a new cold-active protease from psychrotrophic bacteria of Western Himalayan glacial soil. Sci Rep 11:12768. https://doi.org/10.1038/s41598-021-92197-w

    Article  Google Scholar 

  51. Baghel VS, Tripathi RD, Ramteke PW, Gopal K, Dwivedi S, Jain RK, Singh SN (2005) Psychrotrophic proteolytic bacteria from cold environment of Gangotri glacier, Western Himalaya, India. Enzyme Microb Technol 36:654–659. https://doi.org/10.1016/j.enzmictec.2004.09.005

    Article  Google Scholar 

  52. Hasanuzzaman M, Umadhay-Briones KM, Zsiros SM, Morita N, Nodasaka Y, Yumoto I, Okuyama H (2004) Isolation, identification, and characterization of a novel, oil-degrading bacterium, Pseudomonas aeruginosa T1. Curr Microbiol 49:108–114. https://doi.org/10.1007/s00284-004-4267-x

    Article  Google Scholar 

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Acknowledgements

The authors would like to acknowledge the support provided by Researchers Supporting Project Number RSP2024R358, King Saud University, Riyadh, Saudi Arabia. All authors appreciate the Dean of the Faculty of Agriculture Wadura, SKUAST-K, for providing the laboratory facilities required to do microbiological analysis. All authors thank the Director of the Centre of Research for Development at the University of Kashmir for providing laboratory help that allowed the molecular work to go successfully.

Funding

The University Grants Commission, New Delhi, financially supported the research through the Junior Research Fellowship under Maulana Azad National Fellowship Scheme under Grant number F1-17.1/2016-2017/MANF-2015-17-JAM-49697.

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BH collected the data, performed the experiments, and prepared the manuscript, ZAB helped in the experimentation and designed the concept, TAS interpreted the data and performed the statistical analysis. KP and RZS performed statistical analysis and wrote, reviewed, and edited the manuscript. All authors read and approved the final manuscript.

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Correspondence to Basharat Hamid or R. Z. Sayyed.

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Hamid, B., Baba, Z.A., Sheikh, T.A. et al. Investigating potential protease activity of psychrotrophic bacteria from a municipal landfill for solid waste management. Biomass Conv. Bioref. (2024). https://doi.org/10.1007/s13399-024-05621-2

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