Effect of ornithine decarboxylase and norspermidine in modulating cell division in the green alga Chlamydomonas reinhardtii
Open accessAbstract
The extensive genetic resources of Chlamydomonas has led to its widespread use as a model system for understanding fundamental processes in plant cells, including rates of cell division potentially modulated through polyamines. Putrescine was the major polyamine in both free (88%) and membrane-bound fractions (93%) while norspermidine was the next most abundant in these fractions accounting for 11% and 6%, respectively. Low levels of diaminopropane, spermidine and spermine were also observed although no cadaverine or norspermine were detected. Ornithine decarboxylase (ODC, EC 4.1.1.17) activity was almost five times higher than arginine decarboxylase (ADC, EC 4.1.1.19) and is the major route of putrescine synthesis. The fluoride analogue of ornithine (α-DFMO) inhibited membrane associated ODC activity whilst simultaneously stimulating cell division in a dose dependent manner. Following exposure to α-DFMO the putrescine content in the cells declined while the norspermidine content increased over two fold. Addition of norspermidine to cultures stimulated cell division mimicking the effects observed using DFMO and also reversed the inhibitory effects of cyclohexylamine on growth. The results reveal that ODC is the major route to polyamine formation in the Chlamydomonas CC-406 cell-wall mutant, in contrast to the preferential ADC route reported for Chlorella vulgaris, suggesting that significant species differences exist in biosynthetic pathways which modulate endogenous polyamine levels in green algae.
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Optimal growth of algae may require supplementation with a wide range of micronutrients such as those found in Hutner's trace elements solution.
“optimal growth may require supplementation with a wide range of micronutrients such as those found in Hutner's trace elements solution”
From Key Targets for Improving Algal Biofuel Production (2021) · cites this paper as [25]
The cultivation methods (accepted manuscript, p. 5) say that Chlamydomonas was grown in TAP medium containing Hutner’s trace elements. The paper does not establish that those elements are required for optimal growth, or assess a wide range of micronutrients. (LLM, conf=0.84)
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Cites
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Lowry, O. H., Rosebrough, N., Farr, A. L., & Randall, R. (1951) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(19)52451-6 · Cited by 315,771 · see citing works
The Chlamydomonas Genome Reveals the Evolution of Key Animal and Plant Functions
Merchant, S., Prochnik, S., Vallon, O., Harris, E. H., Karpowicz, S. J., Witman, G., Terry, A., Salamov, A., Fritz-Laylin, L., Maréchal-Drouard, L., et al. (2007) · Science · doi:10.1126/science.1143609 · Cited by 2,765 · see citing works
Polyamines: molecules with regulatory functions in plant abiotic stress tolerance
Alcázar, R., Altabella, T., Marco, F., Bortolotti, C., Reymond, M., Koncz, C., Carrasco, P., & Tiburcio, A. F. (2010) · Planta · doi:10.1007/s00425-010-1130-0 · Cited by 1,139 · see citing works
Polyamines: essential factors for growth and survival
Kusano, T., Berberich, T., Tateda, C., & Takahashi, Y. (2008) · Planta · doi:10.1007/s00425-008-0772-7 · Cited by 896 · see citing works
Polyamines and abiotic stress: recent advances
Groppa, M. D., & Benavides, M. P. (2007) · Amino Acids · doi:10.1007/s00726-007-0501-8 · Cited by 788 · see citing works
Wiechelman, K. J., Braun, R. D., & Fitzpatrick, J. D. (1988) · Analytical Biochemistry · doi:10.1016/0003-2697(88)90383-1 · Cited by 766 · see citing works
Evolution and Diversity of Plant Cell Walls: From Algae to Flowering Plants
Popper, Z. A., Michel, G., Hervé, C., Domozych, D. S., Willats, W. G. T., Tuohy, M. G., Kloareg, B., & Stengel, D. B. (2011) · Annual Review of Plant Biology · doi:10.1146/annurev-arplant-042110-103809 · Cited by 732 · see citing works
C HLAMYDOMONAS AS A M ODEL O RGANISM
Harris, E. H. (2001) · Annual Review of Plant Physiology and Plant Molecular Biology · doi:10.1146/annurev.arplant.52.1.363 · Cited by 711 · see citing works
Regulation of Ornithine Decarboxylase
Pegg, A. E. (2006) · Journal of Biological Chemistry · doi:10.1074/jbc.r500031200 · Cited by 477 · see citing works
Phenolamides: Bridging polyamines to the phenolic metabolism
Bassard, J.-E., Ullmann, P., Bernier, F., & Werck-Reichhart, D. (2010) · Phytochemistry · doi:10.1016/j.phytochem.2010.08.003 · Cited by 300 · see citing works
Polyamines in Microalgae: Something Borrowed, Something New
Lin, H., & Lin, H. ‐. (2018) · Marine Drugs · doi:10.3390/md17010001 · Cited by 248 · see citing works
Lee, J., Sperandio, V., Frantz, D. E., Longgood, J. C., Camilli, A., Phillips, M. A., & Michael, A. J. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m900110200 · Cited by 186 · see citing works
Polyamine biosynthetic diversity in plants and algae
Fuell, C., Elliott, K. A., Hanfrey, C. C., et al. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.02.008 · Cited by 182 · see citing works
Differential and functional interactions emphasize the multiple roles of polyamines in plants
Handa, A. K., & Mattoo, A. K. (2010) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2010.02.009 · Cited by 149 · see citing works
Tavladoraki, P., Cona, A., Federico, R., TEMPERA, G., Viceconte, N., Saccoccio, S., Battaglia, V., Toninello, A., & Agostinelli, E. (2011) · Amino Acids · doi:10.1007/s00726-011-1012-1 · Cited by 146 · see citing works
Tassoni, A., van Buuren, M. L., Franceschetti, M., Fornalé, S., & Bagni, N. (2000) · Plant Physiology and Biochemistry · doi:10.1016/s0981-9428(00)00757-9 · Cited by 143 · see citing works
Self-citationThermospermine is Not a Minor Polyamine in the Plant Kingdom
Takano, A., Kakehi, J.-I., & Takahashi, T. (2012) · Plant and Cell Physiology · doi:10.1093/pcp/pcs019 · Cited by 140 · see citing works
The role of polyamines during in vivo and in vitro development
Baron, K. N., & Stasolla, C. (2008) · In Vitro Cellular & Developmental Biology - Plant · doi:10.1007/s11627-008-9176-4 · Cited by 123 · see citing works
Cell wall composition of chlorococcal algae
Blumreisinger, M., Meindl, D., & Loos, E. (1983) · Phytochemistry · doi:10.1016/0031-9422(83)80096-x · Cited by 106 · see citing works
Theiss, C., Bohley, P., & Voigt, J. (2002) · PLANT PHYSIOLOGY · doi:10.1104/pp.010896 · Cited by 97 · see citing works
Widespread Occurrence of Norspermidine and Norspermine in Eukaryotic Algae
Hamana, K., & Matsuzaki, S. (1982) · The Journal of Biochemistry · doi:10.1093/oxfordjournals.jbchem.a133818 · Cited by 88 · see citing works
Vítová, M., Bišová, K., Umysová, D., Hlavová, M., Kawano, S., Zachleder, V., & Čížková, M. (2010) · Planta · doi:10.1007/s00425-010-1282-y · Cited by 75 · see citing works
Ikai, H., & Yamamoto, S. (1997) · Journal of Bacteriology · doi:10.1128/jb.179.16.5118-5125.1997 · Cited by 73 · see citing works
Arginase Is Inoperative in Developing Soybean Embryos1
Goldraij, A., & Polacco, J. C. (1999) · PLANT PHYSIOLOGY · doi:10.1104/pp.119.1.297 · Cited by 71 · see citing works
Norspermidine Is Not a Self-Produced Trigger for Biofilm Disassembly
Hobley, L., Kim, S. H., Maezato, Y., Wyllie, S., Fairlamb, A. H., Stanley‐Wall, N. R., & Michael, A. J. (2014) · Cell · doi:10.1016/j.cell.2014.01.012 · Cited by 70 · see citing works
Vítová, M., Bišová, K., Hlavová, M., Kawano, S., Zachleder, V., & Čížková, M. (2011) · Planta · doi:10.1007/s00425-011-1427-7 · Cited by 69 · see citing works
Regulatory mechanisms of polyamine biosynthesis in plants
Carbonell, J., & Blázquez, M. A. (2009) · Genes & Genomics · doi:10.1007/bf03191144 · Cited by 40 · see citing works
Polyamine metabolism and biosynthetic gene expression in Arabidopsis thaliana under salt stress
Bagni, N., Ruiz, K. B., Franceschetti, M., et al. (2006) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2006.10.011 · Cited by 34 · see citing works
Hamana, K., Aizaki, T., Arai, E., Saito, A., 内方, 薫., & Ohnishi, H. (2004) · The Journal of General and Applied Microbiology · doi:10.2323/jgam.50.289 · Cited by 28 · see citing works
Cloning and characterization of a gene encoding an actin-related protein in Chlamydomonas
Lee, V. D., Finstad, S. L., & Huang, B. (1997) · Gene · doi:10.1016/s0378-1119(97)00254-0 · Cited by 24 · see citing works
Voigt, J., Deinert, B., & Bohley, P. (2000) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2000.108004353.x · Cited by 23 · see citing works
Voigt, J., Deinert, B., & Bohley, P. (2000) · Physiologia Plantarum · doi:10.1034/j.1399-3054.2000.t01-1-100403.x · Cited by 21 · see citing works
Cohen, E., Arad, S. M., Heimer, Y. M., et al. (1983) · Plant and Cell Physiology · doi:10.1093/oxfordjournals.pcp.a076601 · Cited by 18 · see citing works
Theiss, C., Bohley, P., Bisswanger, H., et al. (2004) · Journal of Plant Physiology · doi:10.1078/0176-1617-00987 · Cited by 18 · see citing works
Inhibition of soil urease activity by amido derivatives of phosphoric and thiophosphoric acids
Liao, C. F. H., & Raines, S. G. (1985) · Plant and Soil · doi:10.1007/bf02197808 · Cited by 17 · see citing works
Hamana, K., Niitsu, M., & Hayashi, H. (2013) · The Journal of General and Applied Microbiology · doi:10.2323/jgam.59.313 · Cited by 12 · see citing works
Sagor, G. H. M., Kusano, T., & Berberich, T. (2019) · Plants · doi:10.3390/plants8040099 · Cited by 11 · see citing works
Interaction between polyamines and cells of the marine unicellular red alga Porphyridium sp.
Scoccianti, V., Bagni, N., Dubinsky, O., et al. (1989) · CINECA IRIS Institutional Research information system (University of Urbino) · Cited by 8 · see citing works
Role of the Polyamine Spermidine as a Precursor for Hypusine Modification in eIF5A
Wolff, E. C., & Park, M. H. (2014) · Springer eBooks · doi:10.1007/978-4-431-55212-3_10 · Cited by 7 · see citing works
Structure and expression of the ornithine decarboxylase gene of Chlamydomonas reinhardtii
Voigt, J., Fausel, M., Bohley, P., et al. (2004) · Microbiological Research · doi:10.1016/j.micres.2004.09.010 · Cited by 7 · see citing works
Amino acid-mediated insulin secretion
Cynober, L. (2003) · CRC Press eBooks · doi:10.1201/9780203010266-31 · Cited by 3 · see citing works
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Key Targets for Improving Algal Biofuel Production
Griffiths, G., Hossain, A. K., Sharma, V., & Duraisamy, G. (2021) · Clean Technologies · doi:10.3390/cleantechnol3040043 · Cited by 49 · see citing works
Self-citationAwad, N., Vega-Estévez, S., & Griffiths, G. (2020) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2020.02.019 · Cited by 20 · see citing works
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- Authors
- Tassoni, A., Awad, N., & Griffiths, G.
- Affiliations
- University of Bologna (IT)
- Aston University (GB)
- Corresponding author
- Tassoni, Annalisa
- Griffiths, Gareth
- Venue
- Plant Physiology and Biochemistry
- Publisher
- Elsevier BV
- Published
- 2018-02
- Volume
- 123
- Pages
- 125-131
- ISSN
- 0981-9428 (ISSN-L)
- OpenAlex
- W2773090100
- Cited by
- 28
- References
- 41
- Citations by year
- 2026: 1 · 2025: 1 · 2024: 5 · 2023: 4 · 2022: 6 · 2021: 4 · 2020: 5 · 2019: 1 · 2018: 1
- FWCI
- 0.78
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Plant Physiology and Biochemistry (publishedVersion)
- PubMed (publishedVersion)
- Aston Publications Explorer (Aston University) (acceptedVersion)
- Archivio istituzionale della ricerca (Alma Mater Studiorum Università di Bologna) (submittedVersion, cc-by-nc-nd)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Polyamine Metabolism and Applications
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Protist diversity and phylogeny
- Physical Sciences › Energy › Renewable Energy, Sustainability and the Environment › Algal biology and biofuel production
- Keywords
- ornithine decarboxylase, norspermidine, polyamines, cell division, Chlamydomonas reinhardtii, putrescine, arginine decarboxylase, cyclohexylamine, polyamine biosynthesis, green algae
- MeSH terms
- Cell Division, Mutation, Ornithine Decarboxylase, Plant Proteins, Putrescine, Chlamydomonas reinhardtii
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