Bioconversion of alkaloids to high-value chemicals: Comparative analysis of newly isolated lupanine degrading strains
- PMID: 29126065
- DOI: 10.1016/j.chemosphere.2017.10.165
Bioconversion of alkaloids to high-value chemicals: Comparative analysis of newly isolated lupanine degrading strains
Abstract
This work explores the potential for development of a lupanine valorization process evaluating different isolated microorganisms for their capacity to metabolize the alkaloid. Ecotoxicological assessment demonstrated that lupanine is toxic for Vibrio fischeri and Daphnia magna exhibiting EC50 values of 89 mg L-1 and 47 mg L-1 respectively, while acting both as growth inhibitor for a monocotyledonous and as promoter for a dicotyledonous plant. Among the eight aerobic and anaerobic strains isolated and identified Rhodococcus rhodochrous LPK211 achieved 81% removal for 1.5 g L-1 lupanine, while no end-products were detected by NMR constituting a promising microorganism for lupanine biodegradation. Moreover, Rhodococcus ruber LPK111 and Rhodococcus sp. LPK311 exhibited 66% and 71% of removal respectively, including potential formation of lupanine N-oxide. Pseudomonas putida LPK411 reached 80% of lupanine removal and generated three fermentation products potentially comprising 17-oxolupanine and lupanine derivatives with open ring structures enabling the development of alkaloid valorization processes.
Keywords: Bioconversion; Biodegradation; Lupanine; Quinolizidine alkaloids; Toxicity assessment.
Copyright © 2017 Elsevier Ltd. All rights reserved.
Similar articles
-
Resolution of alkaloid racemate: a novel microbial approach for the production of enantiopure lupanine via industrial wastewater valorization.Microb Cell Fact. 2020 Mar 14;19(1):67. doi: 10.1186/s12934-020-01324-1. Microb Cell Fact. 2020. PMID: 32169079 Free PMC article.
-
Mass spectrometry of bis-quinolizidine alkaloids: 2- and 17-alkyl-substituted derivatives of sparteine and lupanine.J Mass Spectrom. 2000 Nov;35(11):1271-7. doi: 10.1002/1096-9888(200011)35:11<1271::AID-JMS58>3.0.CO;2-8. J Mass Spectrom. 2000. PMID: 11114084
-
New mammalian metabolites of sparteine.Life Sci. 1990;47(4):319-25. doi: 10.1016/0024-3205(90)90590-n. Life Sci. 1990. PMID: 2388532
-
Bacterial removal of quinolizidine alkaloids and other carbon sources from a Lupinus albus aqueous extract.J Agric Food Chem. 2002 Apr 10;50(8):2318-23. doi: 10.1021/jf011371h. J Agric Food Chem. 2002. PMID: 11929291
-
Quinolizidine-Type Alkaloids: Chemodiversity, Occurrence, and Bioactivity.ACS Omega. 2023 Jul 28;8(31):27862-27893. doi: 10.1021/acsomega.3c02179. eCollection 2023 Aug 8. ACS Omega. 2023. PMID: 37576649 Free PMC article. Review.
Cited by
-
Greener Strategy for Lupanine Purification from Lupin Bean Wastewaters Using a Molecularly Imprinted Polymer.ACS Appl Mater Interfaces. 2022 Apr 27;14(16):18910-18921. doi: 10.1021/acsami.2c02053. Epub 2022 Apr 14. ACS Appl Mater Interfaces. 2022. PMID: 35420019 Free PMC article.
-
Screening method and metabolic analysis of plant anti-aging microorganisms via ammonia-induced senescence in the duckweed Wolffia microscopica.Front Plant Sci. 2024 Nov 13;15:1480588. doi: 10.3389/fpls.2024.1480588. eCollection 2024. Front Plant Sci. 2024. PMID: 39619847 Free PMC article.
-
Genome Sequence Analysis of Two Pseudomonas putida Strains to Identify a 17-Hydroxylase Putatively Involved in Sparteine Degradation.Curr Microbiol. 2018 Dec;75(12):1649-1654. doi: 10.1007/s00284-018-1573-2. Epub 2018 Sep 28. Curr Microbiol. 2018. PMID: 30267141 Free PMC article.
-
Resolution of alkaloid racemate: a novel microbial approach for the production of enantiopure lupanine via industrial wastewater valorization.Microb Cell Fact. 2020 Mar 14;19(1):67. doi: 10.1186/s12934-020-01324-1. Microb Cell Fact. 2020. PMID: 32169079 Free PMC article.
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources