Continuous production of chitooligosaccharides in a column reactor by the PUF-immobilized whole cell enzymes of Mucor circinelloides IBT-83.


Journal

Microbial cell factories
ISSN: 1475-2859
Titre abrégé: Microb Cell Fact
Pays: England
ID NLM: 101139812

Informations de publication

Date de publication:
28 Sep 2024
Historique:
received: 08 04 2024
accepted: 13 09 2024
medline: 29 9 2024
pubmed: 29 9 2024
entrez: 28 9 2024
Statut: epublish

Résumé

Chitosan oligosaccharides (COS) have great potential for applications in several fields, including agriculture, food industry or medicine. Nevertheless, the large-scale use of COS requires the development of cost-effective technologies for their production. The main objective of our investigation was to develop an effective method of enzymatic degradation of chitosan in a column reactor using Mucor circinelloides IBT-83 cells, immobilized in a polyurethane foam (PUF). These cells serve as a source of chitosanolytic enzymes. The study revealed that the process of freeze-drying of immobilized mycelium increases the stability of the associated enzymes during chitosan hydrolysis. The use of stabilized preparations as an active reactor bed enables the production of COS at a constant level for 16 reactor cycles (384 h in total), i.e. 216 h longer compared to non-stabilized mycelium. In the hydrolysate, oligomers ranging in structure from dimer to hexamer as well as D-glucosamine were detected. The potential application of the obtained product in agriculture has been verified. The results of phytotests have demonstrated that the introduction of COS into the soil at a concentration of 0.01 or 0.05% w/w resulted in an increase in the growth of Lepidium sativum stem and root, respectively (extensions by 38 and 44% compared to the control sample). The research has verified that the PUF-immobilized M. circinelloides IBT-83 mycelium, which has been stabilized through freeze-drying, is a promising biocatalyst for the environmentally friendly and efficient generation of COS. This biocatalyst has the potential to be used in fertilizers.

Sections du résumé

BACKGROUND BACKGROUND
Chitosan oligosaccharides (COS) have great potential for applications in several fields, including agriculture, food industry or medicine. Nevertheless, the large-scale use of COS requires the development of cost-effective technologies for their production. The main objective of our investigation was to develop an effective method of enzymatic degradation of chitosan in a column reactor using Mucor circinelloides IBT-83 cells, immobilized in a polyurethane foam (PUF). These cells serve as a source of chitosanolytic enzymes.
RESULTS RESULTS
The study revealed that the process of freeze-drying of immobilized mycelium increases the stability of the associated enzymes during chitosan hydrolysis. The use of stabilized preparations as an active reactor bed enables the production of COS at a constant level for 16 reactor cycles (384 h in total), i.e. 216 h longer compared to non-stabilized mycelium. In the hydrolysate, oligomers ranging in structure from dimer to hexamer as well as D-glucosamine were detected. The potential application of the obtained product in agriculture has been verified. The results of phytotests have demonstrated that the introduction of COS into the soil at a concentration of 0.01 or 0.05% w/w resulted in an increase in the growth of Lepidium sativum stem and root, respectively (extensions by 38 and 44% compared to the control sample).
CONCLUSIONS CONCLUSIONS
The research has verified that the PUF-immobilized M. circinelloides IBT-83 mycelium, which has been stabilized through freeze-drying, is a promising biocatalyst for the environmentally friendly and efficient generation of COS. This biocatalyst has the potential to be used in fertilizers.

Identifiants

pubmed: 39342287
doi: 10.1186/s12934-024-02529-4
pii: 10.1186/s12934-024-02529-4
doi:

Substances chimiques

Chitosan 9012-76-4
Oligosaccharides 0
oligochitosan 0
Polyurethanes 0
polyurethane foam 9009-54-5
Enzymes, Immobilized 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

258

Informations de copyright

© 2024. The Author(s).

Références

Gierszewska M, Struszczyk-Świta K, Hudson S. Chitin and chitosan. In: Seidel A, editor. Encyclopedia of Polymer Science and Technology. Wiley; 2021. pp. 1–16. https://doi.org/10.1002/0471440264.pst052.pub2
Hudson S. The outlook for chitosan in textiles: a review of the literature since the start of the 2020’s. PCACD. 2023;28:7. https://doi.org/10.15259/PCACD.28.001
doi: 10.15259/PCACD.28.001
Kaczmarek MB, Struszczyk-Świta K, Li X, Szczęsna-Antczak M, Daroch M. Enzymatic modifications of chitin, Chitosan, and Chitooligosaccharides. Front Bioeng Biotechnol. 2019;7:243. https://doi.org/10.3389/fbioe.2019.00243
doi: 10.3389/fbioe.2019.00243 pubmed: 31612131 pmcid: 6776590
Piekarska K, Sikora M, Owczarek M, Jóźwik-Pruska J, Wiśniewska-Wrona M. Chitin and Chitosan as polymers of the Future-Obtaining, Modification, Life Cycle Assessment and Main directions of application. Polymers. 2023;15:793. https://doi.org/10.3390/polym15040793
doi: 10.3390/polym15040793 pubmed: 36850077 pmcid: 9959150
Yadav M, Goswami P, Paritosh K, Kumar M, Pareek N, Vivekanand V. Seafood waste: a source for preparation of commercially employable chitin/chitosan materials. Bioresour Bioprocess. 2019;6:8. https://doi.org/10.1186/s40643-019-0243-y
doi: 10.1186/s40643-019-0243-y
Hao W, Li K, Li P. Review: advances in preparation of chitooligosaccharides with heterogeneous sequences and their bioactivity. Carbohydr Polym. 2021;252:117206. https://doi.org/10.1016/j.carbpol.2020.117206
doi: 10.1016/j.carbpol.2020.117206 pubmed: 33183640
Lodhi G, Kim J-S, Hwang J-W, Kim S-K, Jeon Y-J, Je J-Y, Ahn C-B, Moon SH, Jeon B-T, Park P-J. Chitooligosaccharide and Its Derivatives: Preparation and Biological Applications. Biomaterials: Chitosan and Collagen for Regenerative Medicine. Hindawi Publishing Corporation, BioMed Research International. 2014; Article ID 654913, https://doi.org/10.1155/2014/654913
Miguez N, Kidibule P, Santos-Moriano P, Ballesteros AO, Fernandez-Lobato M, Plou FJ. Enzymatic synthesis and characterization of different families of Chitooligosaccharides and their Bioactive properties. Appl Sci. 2021;11(7):3212. https://doi.org/10.3390/app11073212
doi: 10.3390/app11073212
Liaqat F, Eltem R. Chitooligosaccharides and their biological activities: a comprehensive review. Carbohydr Polym. 2018;184:243–59. https://doi.org/10.1016/j.carbpol.2017.12.067
doi: 10.1016/j.carbpol.2017.12.067 pubmed: 29352917
Chapelle C, David G, Caillol S, Negrell C. Desroches Le Foll M. Advances in chitooligosaccharides chemical modifications. Biopolymers. 2021;112(9). https://doi.org/10.1002/bip.23461
Struszczyk K, Szczęsna-Antczak M, Walczak M, Pomianowska E, Antczak T. Isolation and purification of Mucor circinelloides intracellular chitosanolytic enzymes. Carbohydr Polym. 2009;78(1):16–24.
doi: 10.1016/j.carbpol.2009.04.010
Kaczmarek MB, Struszczyk-Świta K, Florczak T, Szczęsna-Antczak M, Antczak T. Isolation, molecular cloning and characterisation of two genes coding chitin deacetylase from Mucor circinelloides IBT-83. PCACD. 2016;21:93–103. 10.15259.PCACD.21.09.
doi: 10.15259/PCACD.21.09
Kaczmarek MB, Struszczyk-Świta K, Szczęsna-Antczak MH, Antczak T, Gierszewska M, Steinbuchel A, Daroch M. Polycistronic expression system for Pichia pastoris composed of chitin deacetylase, chitinase, and chitosanase enabling one-pot enzymatic modification of chitin substrates. Front Bioeng Biotechnol. 2021;9:710922. https://doi.org/10.3389/fbioe.2021.710922
doi: 10.3389/fbioe.2021.710922 pubmed: 34490223 pmcid: 8418187
Struszczyk K, Szczęsna-Antczak M, Walczak M, Pomianowska E, Wojciechowska J, Antczak T. Enzymatic preparations from Mucor moulds and their application in oligoaminosaccharides production. PCACD. 2009;14:89–100.
Struszczyk K, Szczęsna-Antczak M, Pomianowska E, Stańczyk Ł, Wojciechowska J, Antczak T. Process of continuous production of oligoaminosaccharides in a column reactor. PCACD. 2010;15:177–88.
Struszczyk-Świta K, Stańczyk Ł, Szczęsna-Antczak M, Antczak T. Scale-up of PUF-immobilized fungal chitosanase–lipase preparation production. Prep Biochem Biotechnol. 2017;47(9):909–17. https://doi.org/10.1080/10826068.2017.1365240
doi: 10.1080/10826068.2017.1365240 pubmed: 28816606
Santos-Moriano P, Woodley JM, Plou FJ. Continuous production of chitooligosaccharides by an immobilized enzyme in a dual-reactor system. J Mol Catal B Enzym. 2016;133:211–7. https://doi.org/10.1016/j.molcatb.2016.09.001
doi: 10.1016/j.molcatb.2016.09.001
Nelson N. A photometric adaptation of the Somogyi method for the determination of glucose. J Biol Chem. 1944;153(2):375–80.
doi: 10.1016/S0021-9258(18)71980-7
Lowry OH, Rosenbrough NJ, Farr AL, Randall RJ. Protein measurement with the Folin phenol reagent. J Biol Chem. 1951;193:265–75.
doi: 10.1016/S0021-9258(19)52451-6 pubmed: 14907713
de Ory I, Cabrera G, Ramirez M, Blandino A. Immobilization of Cell on Polyurethane Foam. In: Guisan JM, editor. Immobilization of Enzymes and Cells. Methods. Mol. Biol. Humana Press Inc. New Jersey; 2008. p. 357-365. https://doi.org/10.1007/978-1-59745-053-9_31
Izume M, Ohtakara A. Preparation of D-glucosamine oligosaccharides by the enzymatic hydrolysis of chitosan. Agric. Biol. Chem. 1987;51:1189–1191. https://doi.org/10.1080/00021369.1987.10868158
Jeon YJ, Park PJ, Byun HG, Song BK, Kim SK. Production of chitosan oligosaccharides using chitin-immobilized enzyme. KSBB J. 1998;13:147–54.
Kuroiwa T, Ichikawa S, Sato S, Hiruta O, Sato S, Mukataka S. Factors affecting the composition of oligosaccharides produced in chitosan hydrolysis using immobilized chitosanases. Biotechnol Prog. 2002;18:969–74. https://doi.org/10.1021/bp020011r
doi: 10.1021/bp020011r pubmed: 12363347
Kuroiwa T, Ichikawa S, Sato S, Mukataka S. Improvement of the yield of physiologically active oligosaccharides in continuous hydrolysis of chitosan using immobilized chitosanases. Biotechnol Bioeng. 2003;84:121–7. https://doi.org/10.1002/bit.10758
doi: 10.1002/bit.10758 pubmed: 12910551
Jeon YJ, Kim SK. Production of chitooligosaccharides using an ultrafiltration membrane reactor and their antibacterial activity. Carbohydr Polym. 2000;41:133–41.
doi: 10.1016/S0144-8617(99)00084-3
Jeon YJ, Kim SK. Antitumor activity of chitosan oligosaccharides produced in an ultra filtration membrane reactor system. J Microbiol Biotechnol. 2002;12:503–7.
Kuroiwa T, Izuta M, Nabetani M, Sato S, Mukataka S, Ichikawa S. Selective and stable production of physiologically active chitosan oligosaccharides using an enzymatic membrane reactor. Process Biochem. 2009;44:283–7. https://doi.org/10.1016/J.PROCBIO.2008.10.020
doi: 10.1016/J.PROCBIO.2008.10.020
Lin Y-W, Hsiao Y-C, Chiang B-H. Production of high degree polymerized chitooligosaccharides in a membrane reactor using purified chitosanase from Bacillus cereus. Food Res Int. 2009;42(9):1355–61. https://doi.org/10.1016/j.foodres.2009.06.008
doi: 10.1016/j.foodres.2009.06.008
Qin Z, Luo S, Li Y, Chen Q, Qiu Y, Zhao L, Jiang L, Zhou J. Biochemical properties of a novel chitosanase from Bacillus amyloliquefaciens and its use in membrane reactor. LWT. 2018;97:9–16. https://doi.org/10.1016/j.lwt.2018.06.027
doi: 10.1016/j.lwt.2018.06.027
Jeon YJ, Kim SK. Continuous production of chitooligosaccharides using a dual reactor system. Process Biochem. 2000;35:623–32.
doi: 10.1016/S0032-9592(99)00118-1
Szczesna-Antczaka M, Antczak T, Rzyska M, Modrzejewska Z, Patura J, Kalinowska H, Bielecki S. Stabilization of an intracellular Mucor circinelloideslipase forapplication in non-aqueous media. J Mol Catal B Enzym. 2004;29:163–71. https://doi.org/10.1016/j.molcatb.2004.02.010
doi: 10.1016/j.molcatb.2004.02.010
Blanch HW, Clark DS. Biochemical Engineering. NewYork: Marcel Dekker, Inc.; 1997.
Ban K, Hama S, Nishizka K, Kaieda M, Matsumato T, Kondo A, Noda A, Fukuda M. Repeated use of whole-cell biocatalysts immobilized within biomass support particles for biodiesel fuel production. J Mol Catal B Enzym. 2002;17:157–65. https://doi.org/10.1016/S1381-1177(02)00023-1
doi: 10.1016/S1381-1177(02)00023-1
Xu L, Qin Y, Song Y, Tang A, Liu Y. Glutaraldehyde-crosslinked Rhizopus oryzae whole cells show improved catalytic performance in alkene epoxidation. Microb Cell Factories. 2023;22:33. https://doi.org/10.1186/s12934-023-02026-0
doi: 10.1186/s12934-023-02026-0
Gonçalves MCP, Morales SAV, Silva ES, Maiorano AE, Perna RF, Kieckbusch TG. Entrapment of glutaraldehyde-crosslinked cells from aspergillus oryzae IPT-301 in calcium alginate for high transfructosylation activity. JCTB. 2020;95(9). https://doi.org/10.1002/jctb.6429
Szczęsna-Antczak M, Struszczyk-Świta K, Rzyska M, Szeląg J, Stańczyk Ł, Antczak T. Oil accumulation and in situ trans/esterification by lipolytic fungal biomass. Bioresour Technol. 2018;265:110–8. https://doi.org/10.1016/j.biortech.2018.05.094
doi: 10.1016/j.biortech.2018.05.094 pubmed: 29885496
Mukhtar Ahmed KB, Khan MMA, Siddiqui H, Jahan A. Chitosan and its oligosaccharides, a promising option for sustainable crop production- a review. Carbohydr Polym. 2020;227:115331. https://doi.org/10.1016/j.carbpol.2019.115331
doi: 10.1016/j.carbpol.2019.115331 pubmed: 31590878
Zhao X, Wang M, Wang W, Liu Q, Li J, Yin H. The application of Chito/Chitin oligosaccharides as Plant vaccines. In: Zhao L, editor. Oligosaccharides of chitin and Chitosan. Springer; 2019. pp. 289–323. https://doi.org/10.1007/978-981-13-9402-7_10
Ma LJ, Li YY, Wang LL, Li XM, Liu T, Bu N. Germination and physiological response of wheat (Triticum aestivum) to presoaking with oligochitosan. Int J Agric Biol. 2014;16:766–70.
Fu X, Zhu L, Li L, Zhang T, Li M, Mou H. Ecofriendly preparation of chitooligosaccharides with diferent degrees of deacetylation from shrimp shell waste and their efects on the germination of wheat seeds. Mar Life Sci Technol. 2019;1:95–103. https://doi.org/10.1007/s42995-019-00012-3
doi: 10.1007/s42995-019-00012-3
Lan W, Wang W, Yu Z, Qin Y, Luan J, Li X. Enhanced germination of barley (Hordeum vulgare L.) using chitooligosaccharide as an elicitor in seed priming to improve malt quality. Biotechnol Lett. 2016;38:1935–40.
doi: 10.1007/s10529-016-2181-5 pubmed: 27465671
Chatelain PG, Pintado ME, Vasconcelos MW. Evaluation of chitooligosaccharide application on mineral accumulation and plant growth in Phaseolus vulgaris. Plant Sci. 2014;215–216:134–40. https://doi.org/10.1016/j.plantsci.2013.11.009
doi: 10.1016/j.plantsci.2013.11.009 pubmed: 24388524

Auteurs

Katarzyna Struszczyk-Świta (K)

Institute of Molecular and Industrial Biotechnology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, 2/22 Stefanowskiego Str., Lodz, 90-537, Poland. katarzyna.struszczyk@p.lodz.pl.

Michał Benedykt Kaczmarek (MB)

Institute of Molecular and Industrial Biotechnology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, 2/22 Stefanowskiego Str., Lodz, 90-537, Poland.

Tadeusz Antczak (T)

Institute of Molecular and Industrial Biotechnology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, 2/22 Stefanowskiego Str., Lodz, 90-537, Poland.

Olga Marchut-Mikołajczyk (O)

Institute of Molecular and Industrial Biotechnology, Faculty of Biotechnology and Food Sciences, Lodz University of Technology, 2/22 Stefanowskiego Str., Lodz, 90-537, Poland.

Articles similaires

Folate-engineered chitosan nanoparticles: next-generation anticancer nanocarriers.

Prashant Kesharwani, Kratika Halwai, Saurav Kumar Jha et al.
1.00
Chitosan Humans Folic Acid Nanoparticles Drug Carriers
Substrate Specificity Peptides Catalysis Hydrolysis Protein Conformation
Fusarium Pigments, Biological Gamma Rays Chitosan Culture Media
Corynebacterium glutamicum Tyramine Metabolic Engineering Phylogeny Fermentation

Classifications MeSH