A THERMOPHILIC L-LACTIC ACID PRODUCER OF HIGH OPTICAL PURITY: ISOLATION AND IDENTIFICATION
Abstract and keywords
Abstract (English):
Biodegradable polymers, specifically polylactide, are an important part of food packaging and medical devices. Microbiological synthesis uses cheap renewable raw materials and industrial waste to produce a high yield of lactic acid, the monomer of polylactide. This method needs new effective lactic acid producing strains, e.g., thermophilic bacteria. The research involved thermophilic bacterial strains isolated from soil and compost samples. Their ability to produce organic acids and extracellular enzymes was tested using the method of high-performance liquid chromatography (HPLC) and microbiological tests respectively. The real-time polymerase chain reaction method (PCR) detected L-lactate dehydrogenase structural genes of L-lactate dehydrogenase of Bacillaceae. Strain T7.1 was fermented using glucose and yeast extract as carbon and nitrogen sources, respectively. The optical purity of lactic acid was evaluated using quantitative gas chromatography on a chiral column to separate lactate isomers. The molecular genetic analysis of the 16S rRNA gene sequence was applied to identify strain T7.1. The chromatographic analysis proved that 10 out of 13 isolated thermophilic strains were effective lactic acid producers. They demonstrated proteolytic, amylolytic, or cellulase activities. During the fermentation, strain T7.1 produced 81 g/L of lactic acid with a peak productivity at 1.58 g/(L·h). The optical purity of the product exceeded 99.9% L-lactate. The genetic analysis identified strain T7.1 as Weizmannia coagulans (Bacillus coagulans). The research revealed a promising thermophilic producer of optically pure L-lactic acid. Further research is needed to optimize the cultivation conditions, design an effective and cheap nutrient medium, and develop engineering and technological solutions to increase the yield.

Keywords:
Thermophilic bacteria, Bacillus, Weizmannia coagulans, lactic acid, L-lactate, polylactide
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References

1. Lactic acid market key players, sales, demand, business strategy and forecast 2030 [Internet]. [cited 2023 Mar 6]. Available from: https://www.digitaljournal.com/pr/lactic-acid-market-key-players-sales-demand-business-strategy-and-forecast-2030#ixzz7uLkASYIk

2. Lactic acid market - Global industry analysis, size, share, growth, trends, regional outlook, and forecast 2022-2030 [Internet]. [cited 2023 Mar 6]. Available from: https://www.precedenceresearch.com/lactic-acid-market

3. Krasnova IS, Ganina VI, Semenov GV. Fruit and vegetable purees as cryoprotectants for vacuum freeze-dried fermented milk products. Foods and Raw Materials. 2023;11(2):300-308. https://doi.org/10.21603/2308-4057-2023-2-578

4. Panseri S, Martino PA, Cagnardi P, Celano G, Tedesco D, Castrica M, et al. Feasibility of biodegradable based packaging used for red meat storage during shelf-life: A pilot study. Food Chemistry. 2018;249:22-29. https://doi.org/10.1016/j.foodchem.2017.12.067

5. Kryuk RV, Kurbanova MG, Kolbina AYu, Plotnikov KB, Plotnikov IB, Petrov AN, et al. Color sensors in smart food packaging. Food Processing: Techniques and Technology. 2022;52(2):321-333. (In Russ.). https://doi.org/10.21603/2074-9414-2022-2-2366

6. Ncube LK, Ude AU, Ogunmuyiwa EN, Zulkifli R, Beas IN. Environmental impact of food packaging materials: A review of contemporary development from conventional plastics to polylactic acid based materials. Materials. 2020;13(21). https://doi.org/10.3390/ma13214994

7. Singha S, Hedenqvist MS. A review on barrier properties of poly(lactic acid)/clay nanocomposites. Polymers. 2020;12(5). https://doi.org/10.3390/polym12051095

8. Farah S, Anderson DG, Langer R. Physical and mechanical properties of PLA, and their functions in widespread applications - A comprehensive review. Advanced Drug Delivery Reviews. 2016;107:367-392. https://doi.org/10.1016/j.addr.2016.06.012

9. Aulitto M, Fusco S, Bartolucci S, Franzén CJ, Contursi P. Bacillus coagulans MA-13: a promising thermophilic and cellulolytic strain for the production of lactic acid from lignocellulosic hydrolysate. Biotechnology for Biofuels and Bioproducts. 2017;10. https://doi.org/10.1186/s13068-017-0896-8

10. Alexandri M, Blanco-Catalá J, Schneider R, Turon X, Venus J. High L(+)-lactic acid productivity in continuous fermentations using bakery waste and lucerne green juice as renewable substrates. Bioresource Technology. 2020;316. https://doi.org/10.1016/j.biortech.2020.123949

11. Hu J, Lin Y, Zhang Z, Xiang T, Mei Y, Zhao S, et al. High-titer lactic acid production by Lactobacillus pentosus FL0421 from corn stover using fed-batch simultaneous saccharification and fermentation. Bioresource Technology. 2016;214:74-80. https://doi.org/10.1016/j.biortech.2016.04.034

12. Kilcawley K, O'Sullivan M. Cheese flavour development and sensory characteristics. In: Papademas P, Bintsis T, editors. Global cheesemaking technology: Cheese quality and characteristics. Wiley; 2017. pp. 45-70. https://doi.org/10.1002/9781119046165.ch0c

13. Poudel P, Tashiro Y, Sakai K. New application of Bacillus strains for optically pure L-lactic acid production: general overview and future prospects. Bioscience, Biotechnology, and Biochemistry. 2016;80(4):642-654. https://doi.org/10.1080/09168451.2015.1095069

14. Urbieta MS, Donati ER, Chan K-G, Shahar S, Sin LL, Goh KM. Thermophiles in the genomic era: Biodiversity, science, and applications. Biotechnology Advances. 2015;33(6):633-647. https://doi.org/10.1016/j.biotechadv.2015.04.007

15. Blumer-Schuette SE, Brown SD, Sander KB, Bayer EA, Kataeva I, Zurawski JV, et al. Thermophilic lignocellulose deconstruction. FEMS Microbiology Reviews. 2014;38(3):393-448. https://doi.org/10.1111/1574-6976.12044

16. Wang Y, Cao W, Luo J, Wan Y. Exploring the potential of lactic acid production from lignocellulosic hydrolysates with various ratios of hexose versus pentose by Bacillus coagulans IPE22. Bioresource Technology. 2018;261:342-349. https://doi.org/10.1016/j.biortech.2018.03.135

17. Bischoff KM, Liu S, Hughes SR, Rich JO. Fermentation of corn fiber hydrolysate to lactic acid by the moderate thermophile Bacillus coagulans. Biotechnology Letters. 2010;32:823-828. https://doi.org/10.1007/s10529-010-0222-z

18. Fan R, Ebrahimi M, Czermak P. Anaerobic membrane bioreactor for continuous lactic acid fermentation. Membranes. 2017;7(2). https://doi.org/10.3390/membranes7020026

19. Ma K, Hu G, Pan L, Wang Z, Zhou Y, Wang Y, et al. Highly efficient production of optically pure l-lactic acid from corn stover hydrolysate by thermophilic Bacillus coagulans. Bioresource Technology. 2016;219:114-122. https://doi.org/10.1016/j.biortech.2016.07.100

20. Thebti W, Riahi Y, Gharsalli R, Belhadj O. Screening and characterization of thermo-active enzymes of biotechnological interest produced by thermophilic Bacillus isolated from hot springs in Tunisia. Acta Biochimica Polonica. 2016;63(3):581-587. https://doi.org/10.18388/abp.2016_1271

21. Tamura K, Stecher G, Kumar S. MEGA11: Molecular evolutionary genetics analysis version 11. Molecular Biology and Evolution. 2021;38(7):3022-3027. https://doi.org/10.1093/molbev/msab120

22. Sun L, Zhang C, Lyu P, Wang Y, Wang L, Yu B. Contributory roles of two l-lactate dehydrogenases for l-lactic acid production in thermotolerant Bacillus coagulans. Scientific Report. 2016;6. https://doi.org/10.1038/srep37916

23. Kuznetsov A, Beloded A, Derunets A, Grosheva V, Vakar L, Kozlovskiy R, et al. Biosynthesis of lactic acid in a membrane bioreactor for cleaner technology of polylactide production. Clean Technologies and Environmental Policy. 2017;19:869-882. https://doi.org/10.1007/s10098-016-1275-z

24. Zhou X, Ye L, Wu JC. Efficient production of L-lactic acid by newly isolated thermophilic Bacillus coagulans WCP10-4 with high glucose tolerance. Applied Microbiology and Biotechnology. 2013;97:4309-4314. https://doi.org/10.1007/s00253-013-4710-7

25. Wang L, Cai Y, Zhu L, Guo H, Yu B. Major role of NAD-dependent lactate dehydrogenases in the production of l-lactic acid with high optical purity by the thermophile Bacillus coagulans. Applied and Environmental Microbiology. 2014;80(23). https://doi.org/10.1128/AEM.01864-14

26. Bosma EF, van de Weijer AHP, van der Vlist L, de Vos WM, van der Oost J, van Kranenburg R. Establishment of markerless gene deletion tools in thermophilic Bacillus smithii and construction of multiple mutant strains. Microbial Cell Factories. 2015;14. https://doi.org/10.1186/s12934-015-0286-5


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