Statistical modelling of micrococcus luteus growth kinetics in microbial lead sulphide (PbS) nanoparticle synthesis via PH-breakpoint and lorentzian models
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OpenAlex topics: Quantum Dots Synthesis And Properties · Metal Extraction and Bioleaching · Coagulation and Flocculation Studies
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1. A. Kumar, T.J. Jayeoye, P. Mohite, S. Singh, T. Rajput, S. Munde, F.N. Eze, V.R. Chidrawar, A. Puri, G. Bhupendra, A. Prajapati, Parihar, Sustainable and consumer-centric nanotechnology-based materials: An update on the multifaceted applications, risks and tremendous opportunities. NSNO. 38, 101148 (2024). https://doi.org/10.1016/j.nanoso.2024.10114810.1016/j.nanoso.2024.101148 ↗
2. S. Roy, R. Kumar, A. Acooli, S. Roy, A. Chatterjee, S. Chattaraj, J. Nayak, B. Jeon, A. Basu, S. Banerjee et al. Transforming nanomaterial synthesis through advanced microfluidic approaches: a review on accessing unrestricted possibilities. J. Compos. Sci. 8, 386 (2024). https://doi.org/10.3390/jcs810038610.3390/jcs8100386 ↗
3. C. Li, Y. Han, X. Zou, X. Zhang, Q. Ran, C. Dong, A systematic discussion and comparison of the construction methods of synthetic microbial community. Synth. Syst. Biotechnol. 9, 775–783 (2024). https://doi.org/10.1016/j.synbio.2024.06.00610.1016/j.synbio.2024.06.006 ↗
4. J. Dai, M.G.Y. Du, M.W. Iqbal, H. Yang, X. Shen, J. Wang, X. Sun, Q. Yuan. Microbial synthesis of nucleosides: advances and prospects. ACS Synth. Biol. 14, 1–9 (2025). https://doi.org/10.1021/acssynbio.4c0053010.1021/acssynbio.4c00530 ↗
5. Antoine, Danchin, Artificial intelligence-based prediction of pathogen emergence and evolution in the world of synthetic biology. Microb. Biotechnol. 17, e70014 (2024). https://doi.org/10.1111/1751-7915.7001410.1111/1751-7915.70014 ↗
6. C. Vandana Singh, S. Pandit, A. Pandit, S. Roy, N.S. Rustagi, H.A. Awwad, Ibrahium, Jigisha Anand, Sumira Malik, Krishna Kumar Yadav, Murtaza Tambuwala. Deciphering the mechanisms and biotechnological implications of nanoparticle synthesis through microbial consortia. J. Basic. Microbiol. 64, e2400035 (2024) https://doi.org/10.1002/jobm.20240003510.1002/jobm.202400035 ↗
7. M. Barani, M. Zeeshan, D. Kalantar-Neyestanaki, M.A. Farooq, A. Rahdar, N.K. Jha, S. Sargazi, P.K. Gupta, V.K. Thakur. Nanomaterials in the management of gram-negative bacterial infections. Nanomaterials. 11, 2535 (2021). https://doi.org/10.3390/nano1110253510.3390/nano11102535 ↗
8. A.A. Hegazy, S.H. Abu-Hussien, N.K. Elsenosy, S.M. El-Sayed, A. El-Naga, Optimization, characterization and biosafety of carotenoids produced from whey using Micrococcus luteus. BMC Biotechnol. 24, 74 (2024). https://pubmed.ncbi.nlm.nih.gov/39375686/10.1186/s12896-024-00899-6 ↗
9. Gail, Betts. Other spoilage bacteria, Food spoilage microorganisms, Chap. 23, Campden and Chorleywood Food Research Association, UK. 668–695 (2006). https://doi.org/10.1533/9781845691417.5.66810.1533/9781845691417.5.668 ↗
10. M. Madigan, J. Martinko. Brock biology of microorganisms, 11th Edn., Prentice Hall. 992 (2005)
11. M. Pichaimani Arunkumar, P. Thanalakshmi, K. Kumar, Premkumar, Micrococcus luteus mediated dual mode synthesis of gold nanoparticles: Involvement of extracellular α-amylase and cell wall teichuronic acid. Colloids Surf. B Biointerfaces. 103, 517–522 (2013). https://doi.org/10.1016/j.colsurfb.2012.10.05110.1016/j.colsurfb.2012.10.051 ↗
12. S. Sakshi Pathak, M. Chaudhary, N. Shrivastav, S. Kumar, M. Varshney, S.K. Kumar, F. Sharma, S. Guzman, C. Kumar, Kumar, The effects of air-annealing on the performance of optical-electrical assessment of sputtered CdS film towards the Ag/n-CdS/p-Si(100)/Al photodetectors. Opt. Mater. 150, 115117 (2024). https://doi.org/10.1016/j.optmat.2024.11511710.1016/j.optmat.2024.115117 ↗
13. A. Hemant Tarkas, D. Rokade, N. Upasani, A. Pardhi, J. Rokade, S.P. Sali, Patole, Sandesh Jadkar, Pioneering method for the synthesis of lead sulfide (PbS) nanoparticles using a surfactant-free microemulsion scheme. RSC Adv. 14, 4352–4361 (2024). https://doi.org/10.1039/D3RA07679B10.1039/D3RA07679B ↗
14. H.J.B.Z.M. Zhang, Microbial synthesis of semiconductor lead sulfide nanoparticles using immobilized Rhodobacter sphaeroides. Mater. Lett. 63, 764–766 (2009). https://doi.org/10.1016/J.MATLET.2008.12.05010.1016/J.MATLET.2008.12.050 ↗
15. M. Kowshik, W. Vogel, J. Urban, S.K. Kulkarni, K.M. Paknikar, Microbial Synthesis of Semiconductor PbS Nanocrystallites. Adv. Mater. Commun. 14, 815–818 (2002). https://doi.org/10.1002/1521-4095(20020605)14:11%3C815::AID-ADMA815%3E3.0.CO;2-K10.1002/1521-4095(20020605)14:11<815::AID-ADMA815>3.0.CO;2-K ↗
16. D. Justin, D.J. Holmes, S. Richardson, R. Saed, D.A. Evans-Gowing, J.R. Russell, Sodeau, Cadmium-specific formation of metal sulfide Q-particles’ by Klebsiella pneumoniae. Microbiology. 143, 2521–2530 (1997). https://doi.org/10.1099/00221287-143-8-252110.1099/00221287-143-8-2521 ↗
17. H. Bai, Z. Zhang, Y. Guo, W. Jia. Biological synthesis of size-controlled cadmium sulfide nanoparticles using immobilized rhodobacter sphaeroides. Nanoscale Res. Lett. 4, 717–723 (2009). https://doi.org/10.1007/s11671-009-9303-010.1007/s11671-009-9303-0 ↗
18. K. Anal, K. Jha, Prasad. PbS nanoparticles: biosynthesis and characterisation, IJNP. 5, 4 (2012). https://doi.org/10.1504/IJNP.2012.04991410.1504/IJNP.2012.049914 ↗
19. K. Sachin Seshadri, M. Saranya, Kowshik, Green synthesis of lead sulfide nanoparticles by the lead resistant marine yeast, Rhodosporidium diobovatum. Formulation Eng. Biomaterials. 27, 1464–1469 (2011). https://doi.org/10.1002/btpr.65110.1002/btpr.651 ↗
20. S. Wei, C. Guo, L. Wang, Bacterial synthesis of PbS nanocrystallites in one-step with l-cysteine serving as both sulfur source and capping ligand. Sci. Rep. 11, 1216 (2021). https://doi.org/10.1038/s41598-020-80450-710.1038/s41598-020-80450-7 ↗
21. S.M. Pourmortazavi, S.S. Hajimirsadeghi, M. Rahimi-Nasrabadi. Statistical Optimization of condition for synthesis lead sulfide nanoparticles. Mater. Manuf. Process. 24, 524–528 (2009). https://doi.org/10.1080/1042691090274016110.1080/10426910902740161 ↗
22. S. Satoko Hiura, K. Koseki, Koyama, Prediction of population behavior of Listeria monocytogenes in food using machine learning and a microbial growth and survival database. Sci. Rep. 11, 10613 (2021). https://doi.org/10.1038/s41598-021-90164-z10.1038/s41598-021-90164-z ↗
23. Marwa, Eltarahony, Esmail El–Fakharany, Marwa Abu–Serie, Marwa ElKady, Amany Ibrahim, Statistical modeling of methylene blue degradation by yeast–bacteria consortium; optimization via agro–industrial waste, immobilization and application in real effluents. Microb. Cell. Factories MCF. 20, 234 (2021). https://doi.org/10.1186/s12934-021-01730-z10.1186/s12934-021-01730-z ↗
24. M. Jennifer, F. Kooken, Karen, Fox, Alvin Fox, Characterization of Micrococcus strains isolated from indoor air. MCP. 26, 1–5 (2012). https://doi.org/10.1016/j.mcp.2011.09.00310.1016/j.mcp.2011.09.003 ↗
25. C.L. Greenblatt, J. Baum, B.Y. Klein, S. Nachshon, V. Koltunov, R.J. Cano. Micrococcus luteus-survival in amber. Microb. Ecol. 48, 120–127 (2004). https://doi.org/10.1007/s00248-003-2016-510.1007/s00248-003-2016-5 ↗
26. J. Sathiya Jeeva, J. Sunitha, R. Ananthalakshmi, S. Rajkumari, M. Ramesh, R. Krishnan, Enzymatic antioxidants and its role in oral diseases. J. Pharm. Bioallied Sci. 7, S331–S333 (2015) . https://doi.org/10.4103/0975-7406.16343810.4103/0975-7406.163438 ↗
27. USBiological Life Sciences. Nutrient broth (powder) catalog no: N8530. Nutrient Broth (Powder) - Data Sheet
28. HIMEDIA. Technical data sheet, HiCrome™ E. coli Agar, M1295. HiCrome™ E. coli Agar
29. American Society for Microbiology (ASM). What stinks? The role of hydrogen sulfide in the gut, stinking it up: h2s production in the gut, what stinks? The role of hydrogen sulfide in the gut
30. Y. Xin, C. Huang, J. Zeng, W. Zhang, Y. Zhou, Y. Xu, Y. Huang, Biochemical mechanism underlying the synthesis of PbS nanoparticle and its in-situ photo effect on Shinella zoogloeoides PQ7. J. Hazard. Mater. 482, 136652 (2025)10.1016/j.jhazmat.2024.136652 ↗
31. S. Bhatnagar, H. Aoyagi, Current overview of the mechanistic pathways and influence of physicochemical parameters on the microbial synthesis and applications of metallic nanoparticles. Bioprocess. Biosyst Eng. 48, 1779–1800 (2025). https://doi.org/10.1007/s00449-025-03190-w10.1007/s00449-025-03190-w ↗
32. C.D. Langa, N. Mabuba, N.C. Hintsho-Mbita. Current progress in the biosynthesis of metal sulfide nanomaterials for the degradation of dyes: a review. Catalysts. 15, 727 (2025). https://doi.org/10.3390/catal1508072710.3390/catal15080727 ↗
33. M. Muloiwa, M. Muloiwa, S. Nyende-Byakika, M. Dinka, S. African, South. Afr. J. Chem. Eng. 33, 141–150 (2020). https://doi.org/10.1016/j.sajce.2020.07.00610.1016/j.sajce.2020.07.006 ↗
34. Y. Dong, X. Yan, F. Lu, M. Guo, Y. Zhuang. Development and optimization of an unstructured kinetic model for sodium gluconate fermentation process. Comput. Mater. Continua. 48, 43–55 (2015). https://doi.org/10.3970/cmc.2015.048.07710.3970/cmc.2015.048.077 ↗
35. Q. Jin, Q. Wu, B.M. Shapiro, S.E. McKernan. Limited mechanistic link between the monod equation and methanogen growth: a perspective from metabolic modeling. Microbiol. Spectr. 10, e02259–e02221 (2022). https://doi.org/10.1128/spectrum.02259-2110.1128/spectrum.02259-21 ↗
36. P.Y. Surekha, P. Dhanya, M.K. Sarath Josh. Micrococcus luteus Strain BAA2, a novel isolate produces carotenoid pigment. Electron. J. Biol. 12, 83–89 (2016)
37. S. Qayyum, S. Basharat, A. Mian, Isolation, identification and antibacterial study of pigmented bacteria. Appl. Nanosci. 10, 4495–4503 (2020). https://doi.org/10.1007/s13204-020-01363-510.1007/s13204-020-01363-5 ↗
38. W.C. Ng, J.R. Brunner, K.C. Rhee. Proteose-peptone fraction of bovine milk: lacteum serum component 3—a whey glycprotein1. J. Dairy. Sci. 53, 987–996 (1970). https://doi.org/10.3168/jds.S0022-0302(70)86334-210.3168/jds.S0022-0302(70)86334-2 ↗
39. A. Koletti, D. Skliros, I. Dervisi, A. Roussis, E. Flemetakis. Oxidative stress responses in microalgae: modern insights into an old topic. Appl. Microbiol. 5(2), 37 (2025). https://doi.org/10.3390/applmicrobiol502003710.3390/applmicrobiol5020037 ↗
40. M. Ashour, M. Ahmed, M. Rabiaab, Shaban, The structure and photoelectrochemical activity of Cr-doped PbS thin films grown by chemical bath deposition. RSC Adv. 10, 12345–12355 (2020). https://doi.org/10.1039/C9RA11042A10.1039/C9RA11042A ↗
41. H. Tarkas, D. Kandivkar, A. Rokade et al., Biogenic synthesis of PbS nanoparticles by Micrococcus luteus and their application in high-performance photodetectors. Sci. Rep. 15, 26993 (2025). https://doi.org/10.1038/s41598-025-12559-610.1038/s41598-025-12559-6 ↗
42. A. Singh, A. Gautam, N. Tyagi et al. Bacterial nanofactories: an in-depth insight to potential green technology. Int. J. Precis Eng. Manuf. -Green Tech. 12, 691–717 (2025). https://doi.org/10.1007/s40684-024-00647-310.1007/s40684-024-00647-3 ↗