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Enhancement of biomass and lipid productivity by overexpression of a bZIP transcription factor in Nannochloropsis salina

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1007/bf02423445openalex-snapshot
A maize DNA-binding factor with a bZIP motif is induced by low temperature
inferredcites →https://doi.org/10.1007/s00253-011-3170-1openalex-snapshot
The effect of light, salinity, and nitrogen availability on lipid production by Nannochloropsis sp.
inferredcites →https://doi.org/10.1007/s00449-011-0639-3openalex-snapshot
Serial optimization of biomass production using microalga Nannochloris oculata and corresponding lipid biosynthesis
inferredcites →https://doi.org/10.1007/s10126-010-9308-9openalex-snapshot
Validation of Housekeeping Genes for Gene Expression Studies in Symbiodinium Exposed to Thermal and Light Stress
inferredcites →https://doi.org/10.1007/s10811-015-0560-2openalex-snapshot
Isolation and screening of euryhaline Tetraselmis spp. suitable for large-scale outdoor culture in hypersaline media for biofuels
inferredcites →https://doi.org/10.1007/s10811-016-0874-8openalex-snapshot
Truncated light-harvesting chlorophyll antenna size in Chlorella vulgaris improves biomass productivity
inferredcites →https://doi.org/10.1007/s12155-012-9269-0openalex-snapshot
De Novo Sequencing and Global Transcriptome Analysis of Nannochloropsis sp. (Eustigmatophyceae) Following Nitrogen Starvation
inferredcites →https://doi.org/10.1016/j.algal.2015.05.003openalex-snapshot
Metabolic engineering toward enhanced LC-PUFA biosynthesis in Nannochloropsis oceanica : Overexpression of endogenous Δ12 desaturase driven by stress-inducible promoter leads to enhanced deposition of polyunsaturated fatty acids in TAG
inferredcites →https://doi.org/10.1016/j.algal.2016.05.015openalex-snapshot
Transcriptome analysis of Chlorella zofingiensis to identify genes and their expressions involved in astaxanthin and triacylglycerol biosynthesis
inferredcites →https://doi.org/10.1016/j.apenergy.2010.12.014openalex-snapshot
Advances and perspectives in using microalgae to produce biodiesel
inferredcites →https://doi.org/10.1016/j.bbagen.2015.10.014openalex-snapshot
Basic leucine zipper (bZIP) transcription factors involved in abiotic stresses: A molecular model of a wheat bZIP factor and implications of its structure in function
inferredcites →https://doi.org/10.1016/j.bbagen.2016.10.027openalex-snapshot
Characterization of Chlamydomonas Ribulose-1,5-bisphosphate carboxylase/oxygenase variants mutated at residues that are post-translationally modified
inferredcites →https://doi.org/10.1016/j.bbrc.2012.06.086openalex-snapshot
Evaluation of putative internal reference genes for gene expression normalization in Nannochloropsis sp. by quantitative real-time RT-PCR
inferredcites →https://doi.org/10.1016/j.biortech.2015.01.040openalex-snapshot
Use of conditioned medium for efficient transformation and cost-effective cultivation of Nannochloropsis salina
inferredcites →https://doi.org/10.1016/j.biotechadv.2014.10.003openalex-snapshot
Microalgal lipids biochemistry and biotechnological perspectives
inferredcites →https://doi.org/10.1016/j.cbpa.2013.04.007openalex-snapshot
Engineering fatty acid biosynthesis in microalgae for sustainable biodiesel
inferredcites →https://doi.org/10.1016/j.copbio.2004.01.009openalex-snapshot
Progress in plant metabolic engineering
inferredcites →https://doi.org/10.1016/j.copbio.2010.03.005openalex-snapshot
Biodiesel from algae: challenges and prospects
inferredcites →https://doi.org/10.1016/j.gene.2013.04.005openalex-snapshot
Transcriptome sequencing, annotation and expression analysis of Nannochloropsis sp. at different growth phases
inferredcites →https://doi.org/10.1016/j.jbiotec.2009.02.018openalex-snapshot
Enhancement of lipid production using biochemical, genetic and transcription factor engineering approaches
inferredcites →https://doi.org/10.1016/j.jbiotec.2012.04.006openalex-snapshot
Functional analysis of three type-2 DGAT homologue genes for triacylglycerol production in the green microalga Chlamydomonas reinhardtii
inferredcites →https://doi.org/10.1016/j.mimet.2009.01.001openalex-snapshot
A high throughput Nile red method for quantitative measurement of neutral lipids in microalgae
inferredcites →https://doi.org/10.1016/j.tibtech.2016.06.001openalex-snapshot
Transcriptional Engineering of Microalgae: Prospects for High-Value Chemicals
inferredcites →https://doi.org/10.1016/s1360-1385(01)02223-3openalex-snapshot
bZIP transcription factors in Arabidopsis
inferredcites →https://doi.org/10.1038/ncomms1688openalex-snapshot
Draft genome sequence and genetic transformation of the oleaginous alga Nannochloropsis gaditana
inferredcites →https://doi.org/10.1038/nmeth.1318openalex-snapshot
Enzymatic assembly of DNA molecules up to several hundred kilobases
inferredcites →https://doi.org/10.1038/srep05454openalex-snapshot
Genome-wide identification of transcription factors and transcription-factor binding sites in oleaginous microalgae Nannochloropsis
inferredcites →https://doi.org/10.1038/srep30444openalex-snapshot
The phylogeny of C/S1 bZIP transcription factors reveals a shared algal ancestry and the pre-angiosperm translational regulation of S1 transcripts
inferredcites →https://doi.org/10.1046/j.1365-313x.2002.01331.xopenalex-snapshot
A WD40‐repeat containing protein, similar to a fungal co‐repressor, is required for transcriptional gene silencing in Chlamydomonas
inferredcites →https://doi.org/10.1073/pnas.1105861108openalex-snapshot
High-efficiency homologous recombination in the oil-producing alga Nannochloropsis sp.
inferredcites →https://doi.org/10.1093/jxb/eri285openalex-snapshot
Housekeeping gene selection for real-time RT-PCR normalization in potato during biotic and abiotic stress
inferredcites →https://doi.org/10.1093/jxb/erw416openalex-snapshot
The plant energy sensor: evolutionary conservation and divergence of SnRK1 structure, regulation, and function
inferredcites →https://doi.org/10.1093/mp/sst120openalex-snapshot
Chromosome Scale Genome Assembly and Transcriptome Profiling of Nannochloropsis gaditana in Nitrogen Depletion
inferredcites →https://doi.org/10.1104/pp.110.157537openalex-snapshot
Expression of ZmLEC1 and ZmWRI1 Increases Seed Oil Production in Maize
inferredcites →https://doi.org/10.1105/tpc.113.121418openalex-snapshot
Choreography of Transcriptomes and Lipidomes of Nannochloropsis Reveals the Mechanisms of Oil Synthesis in Microalgae
inferredcites →https://doi.org/10.1111/j.0022-3646.1995.01004.xopenalex-snapshot
GENETIC TRANSFORMATION OF THE DIATOMS CYCLOTELLA CRYPTICA AND NAVICULA SAPROPHILA
inferredcites →https://doi.org/10.1139/m62-029openalex-snapshot
STUDIES OF MARINE PLANKTONIC DIATOMS: I. CYCLOTELLA NANA HUSTEDT, AND DETONULA CONFERVACEA (CLEVE) GRAN.
inferredcites →https://doi.org/10.1186/1471-2229-9-84openalex-snapshot
Selection of reference genes for quantitative real-time PCR expression studies in the apomictic and sexual grass Brachiaria brizantha
inferredcites →https://doi.org/10.1186/1754-6834-7-110openalex-snapshot
Glycerol and neutral lipid production in the oleaginous marine diatom Phaeodactylum tricornutum promoted by overexpression of glycerol-3-phosphate dehydrogenase
inferredcites →https://doi.org/10.1186/s12862-016-0598-zopenalex-snapshot
The diversification of the basic leucine zipper family in eukaryotes correlates with the evolution of multicellularity
inferredcites →https://doi.org/10.1186/s13068-015-0337-5openalex-snapshot
Generation of random mutants to improve light-use efficiency of Nannochloropsis gaditana cultures for biofuel production
inferredcites →https://doi.org/10.1186/s13068-015-0386-9openalex-snapshot
Effects of overexpression of a bHLH transcription factor on biomass and lipid production in Nannochloropsis salina
inferredcites →https://doi.org/10.1371/journal.pgen.1004094openalex-snapshot
Nannochloropsis Genomes Reveal Evolution of Microalgal Oleaginous Traits
inferredcites →https://doi.org/10.1371/journal.pone.0002944openalex-snapshot
The Role of bZIP Transcription Factors in Green Plant Evolution: Adaptive Features Emerging from Four Founder Genes
inferredcites →https://doi.org/10.1534/genetics.107.086090openalex-snapshot
Green Transcription Factors: A Chlamydomonas Overview
inferredcites →https://doi.org/10.3389/fmicb.2015.01376openalex-snapshot
In Metabolic Engineering of Eukaryotic Microalgae: Potential and Challenges Come with Great Diversity
inferredcites →https://doi.org/10.3389/fpls.2016.00067openalex-snapshot
Recent Advances in Utilizing Transcription Factors to Improve Plant Abiotic Stress Tolerance by Transgenic Technology
inferredcites →https://doi.org/10.3390/md14040061openalex-snapshot
Lipid Production from Nannochloropsis

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4805596openalex-extracted
The Expression of Transcription Factor Wrinkled1 of Dunal-Iella.Salina Promotes the Accumulation of Lipids in Auxenochlorella Protothecoides
inferred← citeshttps://doi.org/10.1002/biot.201900043openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/biot.202100214openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/biot.202100603openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/bit.26894openalex-snapshot
Increased biomass and lipid production by continuous cultivation of Nannochloropsis salina transformant overexpressing a bHLH transcription factor
inferred← citeshttps://doi.org/10.1002/bit.27110openalex-snapshot
Potentiation of concurrent expression of lipogenic genes by novel strong promoters in the oleaginous microalga Phaeodactylum tricornutum
inferred← citeshttps://doi.org/10.1002/mlf2.12097openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/124_2019_30openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s00299-018-2270-0openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10811-019-01768-yopenalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10811-020-02350-7openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s10811-023-03141-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/s11101-022-09804-5openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-90631-9.00017-xopenalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-323-96142-4.00010-5openalex-snapshot
Metabolism of microalgae and metabolic engineering for biomaterial applications
inferred← citeshttps://doi.org/10.1016/b978-0-443-13927-7.00010-4openalex-snapshot
Genetic engineering of microalgae for production of biofuels: Recent progress and practical limitations
inferred← citeshttps://doi.org/10.1016/b978-0-443-29262-0.00022-8openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-29262-0.00028-9openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-29269-9.00007-1openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/b978-0-443-34137-3.00006-6openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2019.101618openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2019.101664openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2020.102158openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2021.102218openalex-snapshot
Enhancement of lipid production in Nannochloropsis salina by overexpression of endogenous NADP-dependent malic enzyme
inferred← citeshttps://doi.org/10.1016/j.algal.2021.102450openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.algal.2022.102728openalex-snapshot
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Oleaginous microalgae Nannochloropsis sp. as a potential source of EPA and bioactive metabolites: Bottlenecks in the downstream processing and unravelling the challenges in its food, feed and therapeutic application
inferred← citeshttps://doi.org/10.1016/j.algal.2025.104192openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biortech.2021.125676openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biortech.2021.126529openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biortech.2024.132004openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biortech.2026.135724openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biotechadv.2020.107554openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.biotechadv.2021.107836openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.freeradbiomed.2023.11.027openalex-snapshot
bZIP transcription factor FabR: Redox-dependent mechanism controlling docosahexaenoic acid biosynthesis and H2O2 stress response in Schizochytrium sp.
inferred← citeshttps://doi.org/10.1016/j.fuel.2021.121169openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.fuel.2022.124567openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jece.2023.110398openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jenvman.2020.111096openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.jphotobiol.2021.112237openalex-snapshot
Expression of the Vitreoscilla hemoglobin gene in Nannochloropsis oceanica regulates intracellular oxygen balance under high-light
inferred← citeshttps://doi.org/10.1016/j.mec.2020.e00142openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.rser.2021.111829openalex-snapshot
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inferred← citeshttps://doi.org/10.1016/j.tibtech.2022.09.002openalex-snapshot
Microalgae-based biotechnological sequestration of carbon dioxide for net zero emissions
inferred← citeshttps://doi.org/10.1021/acs.jafc.0c01284openalex-snapshot
Functional Characterization of Long-Chain Acyl-CoA Synthetase Gene Family from the Oleaginous Alga Chromochloris zofingiensis
inferred← citeshttps://doi.org/10.1021/acs.jafc.3c05290openalex-snapshot
Overexpression of a MYB1 Transcription Factor Enhances Triacylglycerol and Starch Accumulation and Biomass Production in the Green Microalga Chlamydomonas reinhardtii
inferred← citeshttps://doi.org/10.1021/acssuschemeng.9b06748openalex-snapshot
Hydrogen Sulfide Improves Lipid Accumulation in Nannochloropsis oceanica through Metabolic Regulation of Carbon Allocation and Energy Supply
inferred← citeshttps://doi.org/10.1038/s41467-022-29337-xopenalex-snapshot
Exploring a blue-light-sensing transcription factor to double the peak productivity of oil in Nannochloropsis oceanica
inferred← citeshttps://doi.org/10.1038/s41598-018-32216-5openalex-snapshot
MAPK/ERK and JNK pathways regulate lipid synthesis and cell growth of Chlamydomonas reinhardtii under osmotic stress, respectively
inferred← citeshttps://doi.org/10.1080/07388551.2025.2503788openalex-snapshot
Transcriptional control in microalgae: co-regulated fatty acid biosynthesis and carbon dioxide fixation
inferred← citeshttps://doi.org/10.1093/hr/uhac022openalex-snapshot
CRISPR/Cas9-mediated mutagenesis of VvbZIP36 promotes anthocyanin accumulation in grapevine ( Vitis vinifera )
inferred← citeshttps://doi.org/10.1101/2020.10.08.332478openalex-snapshot
Genome engineering of Nannochloropsis with large deletions for constructing microalgal minigenomes
inferred← citeshttps://doi.org/10.1101/2025.08.05.668592openalex-snapshot
Multi-omics decipher the molecular mechanisms driving high-lipid production in an artificially-evolved Chlamydomonas mutant
inferred← citeshttps://doi.org/10.1111/gcbb.13136openalex-snapshot
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inferred← citeshttps://doi.org/10.1111/tpj.14302openalex-snapshot
Multiomics analysis reveals a distinct mechanism of oleaginousness in the emerging model alga Chromochloris zofingiensis
inferred← citeshttps://doi.org/10.1111/tpj.15227openalex-snapshot
Genome engineering of Nannochloropsis with hundred‐kilobase fragment deletions by Cas9 cleavages
inferred← citeshttps://doi.org/10.1126/sciadv.aau3795openalex-snapshot
Transcriptional regulation of microalgae for concurrent lipid overproduction and secretion
inferred← citeshttps://doi.org/10.1128/msphere.00351-24openalex-snapshot
The basic leucine zipper domain (bZIP) transcription factor BbYap1 promotes evasion of host humoral immunity and regulates lipid homeostasis contributing to fungal virulence in Beauveria bassiana
inferred← citeshttps://doi.org/10.1186/s12863-024-01270-6openalex-snapshot
Genome-wide profiling of bZIP transcription factors in Camelina sativa: implications for development and stress response
inferred← citeshttps://doi.org/10.1186/s12864-019-6092-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12934-018-1019-3openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s12934-024-02560-5openalex-snapshot
High-throughput optimization of organic carbon provision strategies enables enhanced arachidonic acid production in novel microalgae
inferred← citeshttps://doi.org/10.1186/s12934-025-02824-8openalex-snapshot
Increasing lipid accumulation in Chlamydomonas by serial knocking out of DYRKP1 kinase and ADP-glucose pyrophosphorylase
inferred← citeshttps://doi.org/10.1186/s12934-025-02893-9openalex-snapshot
Heterologous expression of AtLEC1 and AtLEC1-LIKE transcription factors redirects carbon flux toward lipid accumulation in diatom
inferred← citeshttps://doi.org/10.1186/s13068-019-1366-2openalex-snapshot
Characterization of type I and type II diacylglycerol acyltransferases from the emerging model alga Chlorella zofingiensis reveals their functional complementarity and engineering potential
inferred← citeshttps://doi.org/10.1186/s13068-019-1462-3openalex-snapshot
Heterologous synthesis of chlorophyll b in Nannochloropsis salina enhances growth and lipid production by increasing photosynthetic efficiency
inferred← citeshttps://doi.org/10.1186/s13068-020-01681-4openalex-snapshot
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inferred← citeshttps://doi.org/10.1186/s13068-023-02358-4openalex-snapshot
Transcriptional insights into Chlorella sp. ABC-001: a comparative study of carbon fixation and lipid synthesis under different CO2 conditions
inferred← citeshttps://doi.org/10.1186/s13068-024-02461-0openalex-snapshot
Microalgae biofuels: illuminating the path to a sustainable future amidst challenges and opportunities
inferred← citeshttps://doi.org/10.21203/rs.3.rs-4778598/v1openalex-snapshot
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inferred← citeshttps://doi.org/10.3389/fbioe.2024.1350722openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biology11101418openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/biology13050292openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/en15041550openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/genes10100824openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms20143448openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms22136996openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms241311041openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms25084375openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/ijms26020769openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md18070360openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md20050285openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/md22050216openalex-snapshot
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inferred← citeshttps://doi.org/10.3390/molecules26247697openalex-snapshot
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inferred← citeshttps://doi.org/10.6084/m9.figshare.26604505openalex-snapshot
Additional file 1 of Transcriptional insights into Chlorella sp. ABC-001: a comparative study of carbon fixation and lipid synthesis under different CO2 conditions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26604508openalex-snapshot
Additional file 2 of Transcriptional insights into Chlorella sp. ABC-001: a comparative study of carbon fixation and lipid synthesis under different CO2 conditions
inferred← citeshttps://doi.org/10.6084/m9.figshare.26604511openalex-snapshot
Additional file 3 of Transcriptional insights into Chlorella sp. ABC-001: a comparative study of carbon fixation and lipid synthesis under different CO2 conditions
inferred← citeshttps://doi.org/10.65582/gti.2026.011openalex-snapshot
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The transition kinetic toward nitrogen deprivation in the marine diatom Phaeodactylum tricornutum : a multidisciplinary approach
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