The DOI matches its Crossref record; 151 of the 152 references it cites were found in a registry or an index.
Terpenoids and Their Biosynthesis in Cyanobacteria
Open accessAbstract
Terpenoids, or isoprenoids, are a family of compounds with great structural diversity which are essential for all living organisms. In cyanobacteria, they are synthesized from the methylerythritol-phosphate (MEP) pathway, using glyceraldehyde 3-phosphate and pyruvate produced by photosynthesis as substrates. The products of the MEP pathway are the isomeric five-carbon compounds isopentenyl diphosphate and dimethylallyl diphosphate, which in turn form the basic building blocks for formation of all terpenoids. Many terpenoid compounds have useful properties and are of interest in the fields of pharmaceuticals and nutrition, and even potentially as future biofuels. The MEP pathway, its function and regulation, and the subsequent formation of terpenoids have not been fully elucidated in cyanobacteria, despite its relevance for biotechnological applications. In this review, we summarize the present knowledge about cyanobacterial terpenoid biosynthesis, both regarding the native metabolism and regarding metabolic engineering of cyanobacteria for heterologous production of non-native terpenoids.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Figures

Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The cited source says what the claim attributes to it.
In the citing paper
“terpenoids from the MEP pathway, which uses pyruvate and glyceraldehyde-3-phosphate as precursors [29]”
From Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression (2026) · cites this paper as [29]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
1 retracted
RETRACTED: Cyanobacteria and microalgae: A positive prospect for biofuels
Parmar, A., Singh, N. K., Pandey, A., Gnansounou, E., & Madamwar, D. (2011) · Bioresource Technology · doi:10.1016/j.biortech.2011.08.030 · Cited by 542
RetractedHandbook of Hydrocarbon and Lipid Microbiology
Timmis, K. N. (2009) · Springer eBooks · doi:10.1007/978-3-540-77587-4 · Cited by 1,959
Engineering a mevalonate pathway in Escherichia coli for production of terpenoids
Martin, V. J. J., Pitera, D. J., Withers, S. T., Newman, J. D., & Keasling, J. D. (2003) · Nature Biotechnology · doi:10.1038/nbt833 · Cited by 1,720
Rohmer, M., Knani, M., Simonin, P., Sutter, B., & Sahm, H. (1993) · Biochemical Journal · doi:10.1042/bj2950517 · Cited by 1,200
Rohmer, M., & Rohmer, M. (1999) · Natural Product Reports · doi:10.1039/a709175c · Cited by 1,193
Microbial engineering for the production of advanced biofuels
Peralta‐Yahya, P., Zhang, F., del Cardayré, S. B., & Keasling, J. D. (2012) · Nature · doi:10.1038/nature11478 · Cited by 1,100
Cytochromes P450: a success story.
Werck‐Reichhart, D., & Feyereisen, R. (2000) · Genome biology · doi:10.1186/gb-2000-1-6-reviews3003 · Cited by 962
Beta-caryophyllene is a dietary cannabinoid.
Gertsch, J., Leonti, M., Raduner, S., Racz, I., Chen, J.-Z., Xie, X.-Q., Altmann, K.-H., Karsak, M., & Zimmer, A. (2008) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0803601105 · Cited by 906
Terpene synthases and the regulation, diversity and biological roles of terpene metabolism
Tholl, D. (2006) · Current Opinion in Plant Biology · doi:10.1016/j.pbi.2006.03.014 · Cited by 886
Isoprenoid biosynthesis: The evolution of two ancient and distinct pathways across genomes
Lange, B. M., Rujan, T., Martin, W., & Croteau, R. (2000) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.240454797 · Cited by 881
Research works printed but not linked: 1
- Ramawat, K.G., and Mérillon, J.-M. (2013). Natural Products, Springer. · DOI
Cited by
Sorted by citations
Singh, R., Parihar, P., Singh, M., Bajguz, A., Kumar, J., Singh, S., Singh, V. P., & Prasad, S. M. (2017) · Frontiers in Microbiology · doi:10.3389/fmicb.2017.00515 · Cited by 399
Natural Products from Cyanobacteria: Focus on Beneficial Activities
Demay, J., Bernard, C., Reinhardt, A., & Marie, B. (2019) · Marine Drugs · doi:10.3390/md17060320 · Cited by 346
Cpf1 Is a Versatile Tool for CRISPR Genome Editing Across Diverse Species of Cyanobacteria
Ungerer, J., & Pakrasi, H. B. (2016) · Scientific Reports · doi:10.1038/srep39681 · Cited by 308
Metabolic engineering of cyanobacteria for the synthesis of commodity products
Angermayr, S. A., Gorchs Rovira, A., & Hellingwerf, K. J. (2015) · Trends in Biotechnology · doi:10.1016/j.tibtech.2015.03.009 · Cited by 273
Gonçalves, A. L. (2021) · Applied Sciences · doi:10.3390/app11020871 · Cited by 280
Recent advances in microbial CO2 fixation and conversion to value-added products
Salehizadeh, H., Yan, N., & Farnood, R. (2020) · Chemical Engineering Journal · doi:10.1016/j.cej.2020.124584 · Cited by 258
Ahanger, M. A., Bhat, J. A., Siddiqui, M. H., Rinklebe, J., & Ahmad, P. (2020) · Journal of Experimental Botany · doi:10.1093/jxb/eraa291 · Cited by 199
Identifying and engineering the ideal microbial terpenoid production host
Moser, S., & Pichler, H. (2019) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-019-09892-y · Cited by 174
Englund, E., Andersen‐Ranberg, J., Miao, R., Hamberger, B. R., & Lindberg, P. (2015) · ACS Synthetic Biology · doi:10.1021/acssynbio.5b00070 · Cited by 152
Self-citationThe Beneficial Effects of Cyanobacterial Co-Culture on Plant Growth
Kollmen, J., & Strieth, D. (2022) · Life · doi:10.3390/life12020223 · Cited by 128
Small molecules in the treatment of COVID-19
Lei, S., Chen, X., Wu, J., Duan, X., & Men, K. (2022) · Signal Transduction and Targeted Therapy · doi:10.1038/s41392-022-01249-8 · Cited by 119
Cyanobacteria as photoautotrophic biofactories of high-value chemicals
Noreña-Caro, D., & Benton, M. G. (2018) · Journal of CO2 Utilization · doi:10.1016/j.jcou.2018.10.008 · Cited by 117
Janssen, A., Kaiser, S., Meißner, K., Brenke, N., Menot, L., & Arbizu, P. M. (2015) · PLoS ONE · doi:10.1371/journal.pone.0117790 · Cited by 105
Orthwein, T., Scholl, J., Spät, P., Lucius, S., Koch, M., Maček, B., Hagemann, M., & Forchhammer, K. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2019988118 · Cited by 96
Cyanobacteria and microalgae in supporting human habitation on Mars
Mapstone, L. J., Leite, M. N., Purton, S., Crawford, I. A., & Dartnell, L. (2022) · Biotechnology Advances · doi:10.1016/j.biotechadv.2022.107946 · Cited by 92
“For example, the model cyanobacterium Synechocystis sp. PCC 6803 has been engineered to produce the terpenoid responsible for lemon flavouring, limonene, which, if expressed in Spirulina, could enhance its flavour (Lin et al., 2017; Pattanaik and Lindberg, 2015).”
Carpine, R., & Sieber, S. (2021) · Current Research in Biotechnology · doi:10.1016/j.crbiot.2021.03.001 · Cited by 101
A Glimpse into the Biosynthesis of Terpenoids
Abdallah, I. I., & Quax, W. J. (2017) · KnE Life Sciences · doi:10.18502/kls.v3i5.981 · Cited by 90
Metabolic engineering of Synechocystis sp. PCC 6803 for improved bisabolene production
Rodrigues, J. S., & Lindberg, P. (2021) · Metabolic Engineering Communications · doi:10.1016/j.mec.2020.e00159 · Cited by 80
Self-citationTailoring cyanobacteria as a new platform for highly efficient synthesis of astaxanthin
Diao, J., Song, X., Zhang, L., Cui, J., Chen, L., & Zhang, W. (2020) · Metabolic Engineering · doi:10.1016/j.ymben.2020.07.003 · Cited by 86
The Biochemistry and Antioxidant Properties of Carotenoids
MERHAN, O. (2017) · InTech eBooks · doi:10.5772/67592 · Cited by 87
Pérez-Carrascal, O. M., Tromas, N., Terrat, Y., Moreno, E., Giani, A., Marques, L. C. B., Fortin, N. Y., & Shapiro, B. J. (2021) · Microbiome · doi:10.1186/s40168-021-01140-8 · Cited by 91
Discovery of an Abundance of Biosynthetic Gene Clusters in Shark Bay Microbial Mats
Chen, R., Wong, H. L., Kindler, G. S., MacLeod, F. I., Benaud, N., Ferrari, B. C., & Burns, B. P. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.01950 · Cited by 80
Synthetic biology for production of natural and new‐to‐nature terpenoids in photosynthetic organisms
Arendt, P., Pollier, J., Callewaert, N., & Goossens, A. (2016) · The Plant Journal · doi:10.1111/tpj.13138 · Cited by 77
Podduturi, R., Petersen, M. A., Mahmud, S. A. S., Rahman, M. M., & Jørgensen, N. O. G. (2017) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.7b00497 · Cited by 76
Encapsulation as a Strategy for the Design of Biological Compartmentalization
Giessen, T. W., & Silver, P. A. (2015) · Journal of Molecular Biology · doi:10.1016/j.jmb.2015.09.009 · Cited by 74
High density cultivation for efficient sesquiterpenoid biosynthesis in Synechocystis sp. PCC 6803
Dienst, D. D., Wichmann, J., Mantovani, O., Rodrigues, J. S., & Lindberg, P. (2020) · Scientific Reports · doi:10.1038/s41598-020-62681-w · Cited by 74
Self-citationEl-Hack, M. E. A., El‐Saadony, M. T., Elbestawy, A. R., Ellakany, H. F., Abaza, S. S., Geneedy, A. M., Salem, H. M., Taha, A. E.-S., Swelum, A. A., Omer, F. A., et al. (2022) · Marine Pollution Bulletin · doi:10.1016/j.marpolbul.2022.113579 · Cited by 71
Hasunuma, T., Takaki, A., Matsuda, M., Kato, Y., Vavricka, C. J., & Kondo, A. (2019) · ACS Synthetic Biology · doi:10.1021/acssynbio.9b00280 · Cited by 63
Current Status and Future Strategies to Increase Secondary Metabolite Production from Cyanobacteria
Jeong, Y., Cho, S.-H., Lee, H., Choi, H., Kim, D., Lee, C., Cho, S., & Cho, B. (2020) · Microorganisms · doi:10.3390/microorganisms8121849 · Cited by 58
The conifer biomarkers dehydroabietic and abietic acids are widespread in Cyanobacteria
Costa, M., Rego, A., Ramos, V., Afonso, T. B., Freitas, S., Preto, M., Lopes, V. R., Vasconcelos, V. M., Magalhães, C., & Leão, P. N. (2016) · Scientific Reports · doi:10.1038/srep23436 · Cited by 62
Secondary Metabolites in Cyanobacteria
Kultschar, B., & Llewellyn, C. A. (2018) · InTech eBooks · doi:10.5772/intechopen.75648 · Cited by 60
Globally distributed marine Gemmatimonadota have unique genomic potentials
Gong, X., Xu, L., Langwig, M. V., Chen, Z., Huang, S., Zhao, D., Su, L., Zhang, Y., Francis, C. A., Liu, J., et al. (2024) · Microbiome · doi:10.1186/s40168-024-01871-4 · Cited by 53
Recent advances in synthetic biology of cyanobacteria for improved chemicals production
Wang, F., Gao, Y., & Yang, G. (2020) · Bioengineered · doi:10.1080/21655979.2020.1837458 · Cited by 49
Continuous photoproduction of hydrocarbon drop-in fuel by microbial cell factories
Moulin, S., Légeret, B., Blangy, S., Sorigué, D. R., Burlacot, A., Auroy, P., Li‐Beisson, Y., Peltier, G., & Beisson, F. (2019) · Scientific Reports · doi:10.1038/s41598-019-50261-6 · Cited by 49
Majee, C., Atriya, A., Mazumder, R., Choudhary, A. N., Salahuddin, S., Mazumder, A., Dahiya, A., & Priya, N. (2022) · Current Pharmaceutical Biotechnology · doi:10.2174/1389201024666221130163116 · Cited by 48
Cybastacines A and B: Antibiotic Sesterterpenes from a Nostoc sp. Cyanobacterium
Cabanillas, A. H., Pérez, V. T., Corral, S. M., Valencia, D. F. R., Quintana, A. M., Doménech, M. O., & Sánchez, Á. R. (2018) · Journal of Natural Products · doi:10.1021/acs.jnatprod.7b00638 · Cited by 48
Llewellyn, C. A., Airs, R. L., Farnham, G., & Greig, C. (2020) · Frontiers in Microbiology · doi:10.3389/fmicb.2020.00163 · Cited by 47
Sebesta, J., & Peebles, C. A. (2020) · Metabolic Engineering Communications · doi:10.1016/j.mec.2019.e00117 · Cited by 46
Versatility of hydrocarbon production in cyanobacteria
Xie, M., Wang, W., Zhang, W., Chen, L., & Lü, X. (2016) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-016-8064-9 · Cited by 45
A diurnal flux balance model of Synechocystis sp. PCC 6803 metabolism
Sarkar, D., Mueller, T. J., Liu, D., Pakrasi, H. B., & Maranas, C. D. (2019) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1006692 · Cited by 44
Potential bacterial bioindicators of urban pollution in mangroves
Torres, G. G., Figueroa-Galvis, I., Muñoz-García, A., Polanía, J., & Vanegas, J. (2019) · Environmental Pollution · doi:10.1016/j.envpol.2019.113293 · Cited by 42
Churro, C., Semedo-Aguiar, A. P., Silva, A., Pereira‐Leal, J. B., & Leite, R. B. (2020) · Scientific Reports · doi:10.1038/s41598-020-64774-y · Cited by 42
Taylor, G. M., Hitchcock, A., & Heap, J. T. (2021) · Nucleic Acids Research · doi:10.1093/nar/gkab791 · Cited by 38
Cyanobacteria: A Promising Source of Antifungal Metabolites
do Amaral, S. C., Xavier, L. P., Vasconcelos, V. M., & Santos, A. V. (2023) · Marine Drugs · doi:10.3390/md21060359 · Cited by 39
6S RNA plays a role in recovery from nitrogen depletion in Synechocystis sp. PCC 6803
Heilmann, B., Hakkila, K., Georg, J., Tyystjärvi, T., Hess, W. R., Axmann, I. M. I., & Dienst, D. D. (2017) · BMC Microbiology · doi:10.1186/s12866-017-1137-9 · Cited by 37
Pattanaik, B., Englund, E., Nolte, N., & Lindberg, P. (2020) · Metabolic Engineering Communications · doi:10.1016/j.mec.2020.e00125 · Cited by 37
Self-citationVerma, S., Thapa, S., Siddiqui, N. M., & Chakdar, H. (2022) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-022-03285-6 · Cited by 38
Loeschcke, A., Dienst, D. D., Wewer, V., Hage‐Hülsmann, J., Dietsch, M., Kranz-Finger, S., Hüren, V., Metzger, S. U., Urlacher, V. B., Gigolashvili, T., et al. (2017) · PLoS ONE · doi:10.1371/journal.pone.0189816 · Cited by 34
Shen, Q., Wang, Q., Miao, H., Shimada, M., Utsumi, M., Lei, Z., Zhang, Z., Nishimura, O., 浅田, 安., Fujimoto, N., et al. (2021) · Environmental Science and Pollution Research · doi:10.1007/s11356-021-16593-5 · Cited by 32
Popin, R. V., Alvarenga, D. O., Castelo‐Branco, R., Fewer, D. P., & Sivonen, K. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.684565 · Cited by 33
Perspectives of cyanobacterial cell factories
Melis, A., Hidalgo Martinez, D. A., & Betterle, N. (2024) · Photosynthesis Research · doi:10.1007/s11120-023-01056-4 · Cited by 31
Pushing the limits of concertedness. A waltz of wandering carbocations
Reis, M. C., López, C. S., Faza, O. N., & Tantillo, D. J. (2018) · Chemical Science · doi:10.1039/c8sc03567a · Cited by 30
Cyanobacteria: Photosynthetic cell factories for biofuel production
Majhi, B. K. (2024) · Journal of Bioresources and Bioproducts · doi:10.1016/j.jobab.2024.10.001 · Cited by 35
Shalu, S., Karthikanath, P. K. R., Vaidyanathan, V. K., Blank, L. M., Germer, A., & Balakumaran, P. A. (2024) · Engineering in Life Sciences · doi:10.1002/elsc.202400003 · Cited by 29
Progress in heterologous biosynthesis of forskolin
Ju, H., Zhang, C., & Lü, W. (2021) · Journal of Industrial Microbiology & Biotechnology · doi:10.1093/jimb/kuab009 · Cited by 28
Kitchener, R. L., & Grunden, A. M. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8755-5 · Cited by 26
Angermayr, S. A., van Alphen, P., Hasdemir, D., Kramer, G., Iqbal, M., van Grondelle, W., Hoefsloot, H. C. J., Choi, Y. H., & Hellingwerf, K. J. (2016) · Applied and Environmental Microbiology · doi:10.1128/aem.00256-16 · Cited by 25
Heterologous production of labdane-type diterpenes in the green alga Chlamydomonas reinhardtii
Papaefthimiou, D., Diretto, G., Demurtas, O. C., Mini, P., Ferrante, P., Giuliano, G., & Kanellis, A. K. (2019) · Phytochemistry · doi:10.1016/j.phytochem.2019.112082 · Cited by 24
Biosynthesis and potential applications of terpenes produced from microalgae
Costa, J. A. V., Cassuriaga, A. P. A., Moraes, L., & de Morais, M. G. (2022) · Bioresource Technology Reports · doi:10.1016/j.biteb.2022.101166 · Cited by 24
Suparmaniam, U., Lam, M. K., Lim, J. W., Tan, I. S., Chin, B. L. F., Shuit, S. H., Lim, S., Pang, Y. L., & Kiew, P. L. (2023) · Biotechnology Advances · doi:10.1016/j.biotechadv.2023.108280 · Cited by 22
Cyanobacteria as a Biocatalyst for Sustainable Production of Biofuels and Chemicals
Singh, V. K., Jha, S., Rana, P., Soni, R., Lalnunpuii, R., Singh, P. K., Sinha, R. P., & Singh, G. (2024) · Energies · doi:10.3390/en17020408 · Cited by 22
Awin, T. M., Mediani, A., Maulidiani, M., Leong, S. W., Faudzi, S. M. M., Shaari, K., & Abas, F. (2019) · Journal of Food Composition and Analysis · doi:10.1016/j.jfca.2019.01.004 · Cited by 22
Altered Carbon Partitioning Enhances CO2 to Terpene Conversion in Cyanobacteria
Li, M., Long, B., Dai, S. Y., Golden, J. W., Wang, X., & Yuan, J. S. (2022) · BioDesign Research · doi:10.34133/2022/9897425 · Cited by 20
Gao, X., Zhu, Z., Xu, H., Liu, L., An, J., Ji, B., & Ye, S. (2020) · Environmental Microbiology · doi:10.1111/1462-2920.15153 · Cited by 20
Hu, J., Ma, H., Gan, N., Wang, H., Lǐ, Y., Wang, L., & Song, L. (2021) · Harmful Algae · doi:10.1016/j.hal.2021.102170 · Cited by 20
Gong, S., Wang, Y., Wang, H., Zhang, X., & Liu, G. (2018) · Journal of Analytical and Applied Pyrolysis · doi:10.1016/j.jaap.2018.09.011 · Cited by 19
Fagundes, M. B., Álvarez‐Rivera, G., Vendruscolo, R. G., Voss, M., da Silva, P. A., Barin, J. S., Lopes, E. J., Zepka, L. Q., & Wagner, R. C. (2020) · Talanta · doi:10.1016/j.talanta.2020.121793 · Cited by 20
Kant, G., Pandey, A., Hasan, A., Bux, F., Kumari, S., & Srivastava, S. (2024) · Process Biochemistry · doi:10.1016/j.procbio.2024.01.027 · Cited by 22
Effects of elevated nitrogen on the growth and geosmin productivity of Dolichospermum smithii
Shen, Q., Shimizu, K., Miao, H., Tsukino, S., Utsumi, M., Lei, Z., Zhang, Z., Nishimura, O., 浅田, 安., Fujimoto, N., et al. (2020) · Environmental Science and Pollution Research · doi:10.1007/s11356-020-10429-4 · Cited by 18
Lehmann, M., Vamvaka, E., Torrado, A., Jahns, P., Dann, M., Rosenhammer, L., Aziba, A., Leister, D., & Rühle, T. (2021) · Frontiers in Plant Science · doi:10.3389/fpls.2021.699424 · Cited by 17
Zhao, J., Chen, K., Palsson, B. Ø., & Yang, L. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011865 · Cited by 19
Photosynthetic Conversion of CO2 Into Pinene Using Engineered Synechococcus sp. PCC 7002
Yang, R., Zhu, L., Li, T., Zhu, L., Ye, Z., & Zhang, D. (2021) · Frontiers in Bioengineering and Biotechnology · doi:10.3389/fbioe.2021.779437 · Cited by 16
Ball, L., Frey, T., Haag, F., Frank, S., Hoffmann, S., Laska, M., Steinhaus, M., Neuhaus, K., & Krautwurst, D. (2024) · Journal of Agricultural and Food Chemistry · doi:10.1021/acs.jafc.4c01515 · Cited by 16
Oliveira, J. S., de Araujo, W. J., de Figueiredo, R. M., Silva-Portela, R. D. C. B., Guerra, A. D. B., Araújo, S. C. D. S., Minnicelli, C., Carlos, A. C., de Vasconcelos, A. T. R., Freitas, A. T., et al. (2017) · BMC Microbiology · doi:10.1186/s12866-017-1077-4 · Cited by 15
Fusion constructs enhance heterologous β-phellandrene production in Synechocystis sp. PCC 6803
Valsami, E., Psychogyiou, M. E., Pateraki, A., Chrysoulaki, E., Melis, A., & Ghanotakis, D. F. (2020) · Journal of Applied Phycology · doi:10.1007/s10811-020-02186-1 · Cited by 14
Insight to biotechnological utility of phycochemicals from cyanobacterium Anabaena sp.: An overview
Mandhata, C. P., Bishoyi, A. K., Sahoo, C. R., Maharana, S., & Padhy, R. N. (2023) · Fitoterapia · doi:10.1016/j.fitote.2023.105594 · Cited by 14
Kapoor, B., Kumar, A., & Kumar, P. (2021) · Molecular Genetics and Genomics · doi:10.1007/s00438-021-01821-x · Cited by 14
Lydon, C. A., Mathivathanan, L., Sanchez, J., dos Santos, L. A. H., Sauvage, T., Gunasekera, S. P., Paul, V. J., & Berry, J. P. (2020) · Journal of Natural Products · doi:10.1021/acs.jnatprod.0c00203 · Cited by 14
Machado, M. J., Jacinavicius, F. R., Médice, R. V., Dextro, R. B., Feitosa, A. M. T., Weiss, M. B., Pellegrinetti, T. A., Cotta, S. R., Crnkovic, C. M., & Fiore, M. F. (2025) · Frontiers in Microbiology · doi:10.3389/fmicb.2025.1582103 · Cited by 14
Collart, L. P., Jiang, D., & Halsey, K. H. (2023) · mSystems · doi:10.1128/msystems.00379-23 · Cited by 13
Ngashangva, N., Mukherjee, P. K., Sharma, C. K., Kalita, M. C., & Sarangthem, I. (2022) · Scientific Reports · doi:10.1038/s41598-022-23613-y · Cited by 13
Plant Essential Oils and Their Constituents for Therapeutic Benefits
Rani, M., Jindal, S., Anand, R., Sharma, N., Ranjan, K. R., Mukherjee, M. D., & Mishra, V. (2023) · doi:10.1002/9781119829614.ch42 · Cited by 13
Foresti, A. C., Scalon, S. D. P. Q., Santos, C. C., Reis, L. C., & Linné, J. A. (2024) · Journal of soil science and plant nutrition · doi:10.1007/s42729-024-01664-6 · Cited by 12
Gonçalves, C. F., Lima, S., Tamagnini, P., & Oliveira, P. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814667-5.00018-0 · Cited by 12
Gomes, L. C., Rana, A., Berglund, M., Wiklund, P., & Ottosson, H. (2023) · Sustainable Energy & Fuels · doi:10.1039/d2se01370c · Cited by 11
Diversity of lipid profiles of Symbiodiniaceae under temperature and nutrient stress
Motta, L. M. L., Padula, M. P., Sommer, B., Camp, E. F., & Matthews, J. L. (2024) · Frontiers in Protistology · doi:10.3389/frpro.2024.1320353 · Cited by 13
Cyanobacterial Bioactive Compounds: Synthesis, Extraction, and Applications
Khan, F. S. A., Akhlaq, A., Rasool, M. H., & Srinuanpan, S. (2024) · Springer eBooks · doi:10.1007/978-3-031-45523-0_9 · Cited by 11
Effects of Cyanobacterial Secondary Metabolites on Phytoplankton Community Succession
Pei, Y., Xu, R., Hilt, S., & Chang, X. (2020) · Reference series in phytochemistry · doi:10.1007/978-3-319-96397-6_12 · Cited by 11
Guan, J., Shen, S., Wu, H., Liu, X., Shen, W., He, Y., & Duan, R. (2017) · World Journal of Microbiology and Biotechnology · doi:10.1007/s11274-016-2199-9 · Cited by 11
Rodrigues, J. S., Bourgade, B., Galle, K. R., & Lindberg, P. (2023) · Microbial Cell Factories · doi:10.1186/s12934-023-02040-2 · Cited by 10
Self-citationElsheikh, S., & Eltanahy, E. (2023) · Elsevier eBooks · doi:10.1016/b978-0-323-95251-4.00002-8 · Cited by 10
Singh, H., Niharika, N., Lamichhane, P., Gupta, R., Kaushik, N., Choi, E. H., & Kaushik, N. K. (2023) · Plant Biotechnology Reports · doi:10.1007/s11816-023-00883-0 · Cited by 11
Engineering Nannochloropsis oceanica for the production of diterpenoid compounds
Du, Z., Bhat, W. W., Poliner, E., Johnson, S. R., Bertucci, C., Farré, E. M., & Hamberger, B. (2023) · mLife · doi:10.1002/mlf2.12097 · Cited by 9
Terpenoids as Natural Allelopathic Compounds in Plants
Jasim, I. R., Alwattar, M. T. H., & Yaqub, H. M. (2023) · Mağallaẗ ʻulūm al-rāfidayn · doi:10.33899/rjs.2023.181275 · Cited by 10
Roles of Terpenoids in Essential Oils and Its Potential as Natural Weed Killers: Recent Developments
Almarie, A. A. (2020) · IntechOpen eBooks · doi:10.5772/intechopen.91322 · Cited by 10
Yang, X., Lou, Y., Song, L., Zhang, D., Song, Y., Liang, J., Liu, Z., Wang, C., & Zhao, Z. (2025) · Plant Physiology and Biochemistry · doi:10.1016/j.plaphy.2025.109529 · Cited by 9
Tantong, S., Incharoensakdi, A., Sirikantaramas, S., & Lindblad, P. C. (2016) · Protein Expression and Purification · doi:10.1016/j.pep.2016.01.020 · Cited by 9
Denitrification shifted autotroph-heterotroph interactions in Microcystis aggregates
Chen, Z., Huang, Y., Shen, Y., Zhang, J., Deng, J., & Chen, X. (2023) · Environmental Research · doi:10.1016/j.envres.2023.116269 · Cited by 9
Insights Into Limnothrix sp. Metabolism Based on Comparative Genomics
Lima, A. R. J., Siqueira, A. S., de Vasconcelos, J. M., Pereira, J. S., de Azevedo, J. S. N., Moraes, P. H. G., Aguiar, D. C. F., de Lima, C. P. S., Júnior, J. L. D. S. G. V., Nunes, M. R. T., et al. (2018) · Frontiers in Microbiology · doi:10.3389/fmicb.2018.02811 · Cited by 9
Wells, K. N., Videau, P., Nelson, D., Eiting, J., & Philmus, B. J. (2018) · FEMS Microbiology Letters · doi:10.1093/femsle/fny164 · Cited by 8
Metadata
- Authors
- Pattanaik, B., & Lindberg, P.
- Affiliations
- Uppsala University (SE)
- Corresponding author
- Lindberg, Pia
- ORCID
- Lindberg, Pia
- Venue
- Life
- Publisher
- MDPI AG
- Published
- 2015-01-21
- Volume
- 5
- Issue
- 1
- Pages
- 269-293
- ISSN
- 2075-1729 (ISSN-L)
- PMC
- PMC4390852
- OpenAlex
- W2058582378
- Cited by
- 173
- References
- 152
- Citations by year
- 2026: 10 · 2025: 9 · 2024: 25 · 2023: 19 · 2022: 15 · 2021: 19 · 2020: 29 · 2019: 13 · 2018: 12 · 2017: 10 · 2016: 8 · 2015: 4
- FWCI
- 1.10
- Type
- journal article
- Language
- en
- Open access
- gold
- doi.org
- Licence
- Locations
- Life (publishedVersion, cc-by)
- Europe PMC (PubMed Central) (publishedVersion, cc-by)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Carl Tryggers Stiftelse för Vetenskaplig Forskning
- Knut och Alice Wallenbergs Stiftelse
- Energimyndigheten
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Plant biochemistry and biosynthesis
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Microbial Metabolic Engineering and Bioproduction
- Life Sciences › Immunology and Microbiology › Applied Microbiology and Biotechnology › Microbial Natural Products and Biosynthesis
- Keywords
- terpenoids, cyanobacteria, methylerythritol phosphate pathway, isopentenyl pyrophosphate, dimethylallyl diphosphate, terpenoid biosynthesis, metabolic engineering, heterologous production, biofuels
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review