Cited by 306Diatoms and Algae ResearchPlant tissue culture and regenerationProtist diversity and phylogeny

The DOI matches its Crossref record; 35 of the 35 references it cites were found in a registry or an index.

GENETIC TRANSFORMATION OF THE DIATOMS CYCLOTELLA CRYPTICA AND NAVICULA SAPROPHILA

Dunahay, Terri G., Jarvis, Eric E., Roessler, Paul G.·1995·Journal of Phycology

DOI 10.1111/j.0022-3646.1995.01004.x

Open this paper in CoChat — free account

Abstract

Two species of diatoms were genetically transformed by introducing plasmid vectors containing the Escherichia coli neomycin phosphotransferase II (npt II)gene. Expression of the bacterial npt II gene in the diatoms was achieved using the putative promoter and terminator sequences from the acetyl‐CoA carboxylase gene from the centric diatom Cyclotella cryptica T13L Reimann, Lewin, and Guillard. The vectors were introduced into C. cryptica and the pennate diatom Navicula saprophila NAVIC1 Lange‐Bertalot and Bonik by microprojectile bombardment. Putative transformants were selected based on their ability to grow in the presence of the antibiotic G418, and production of the neomycin phosphotransferase protein by the transformed cells was confirmed by western blotting. The foreign DNA integrated into one or more random sites within the genome of the transformed algal cells, often in the form of tandem repeats. This is the first report of reproducible, stable genetic transformation of a chlorophyll c‐containing alga.

Integrity signals

Registry

Crossref · 10.1111/j.0022-3646.1995.01004.x

Cites

35 of 35 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

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?

Rapid isolation of high molecular weight plant DNA
Murray, M. G., & Thompson, W. F. (1980) · Nucleic Acids Research · doi:10.1093/nar/8.19.4321 · Cited by 12,156
[1] Production of single-stranded plasmid DNA
Vieira, J., & Messing, J. W. (1987) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(87)53044-0 · Cited by 2,558
Global climate change and terrestrial net primary production
Melillo, J. M., McGuire, A. D., Kicklighter, D. W., Moore, B., Vörösmarty, C. J., & Schloss, A. L. (1993) · Nature · doi:10.1038/363234a0 · Cited by 1,955
The Silica Balance in the World Ocean: A Reestimate
Tréguer, P. J., Nelson, D. M., Bennekom, A. J. V., DeMaster, D. J., Leynaert, A., & Quéguiner, B. (1995) · Science · doi:10.1126/science.268.5209.375 · Cited by 1,489
High-frequency nuclear transformation of Chlamydomonas reinhardtii.
Kindle, K. L. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.3.1228 · Cited by 1,097
Transient and Stable Expression of the Firefly Luciferase Gene in Plant Cells and Transgenic Plants
Ow, D. W., Wood, K. V., DeLuca, M. A., de Wet, J. R., Helinski, D. R., & Howell, S. H. (1986) · Science · doi:10.1126/science.234.4778.856 · Cited by 725
[36] Optimizing the biolistic process for different biological applications
Sanford, J. C., Smith, F. D., & Russell, J. A. (1993) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/0076-6879(93)17086-k · Cited by 643
Stable transformation of maize after gene transfer by electroporation
Fromm, M. E., Taylor, L. P., & Walbot, V. (1986) · Nature · doi:10.1038/319791a0 · Cited by 639
Transgenic expression of aminoglycoside adenine transferase in the chloroplast: a selectable marker for site-directed transformation of chlamydomonas
Goldschmidt‐Clermont, M. (1991) · Nucleic Acids Research · doi:10.1093/nar/19.15.4083 · Cited by 473
Transformation in fungi
Fincham, J. R. (1989) · Microbiological Reviews · doi:10.1128/mr.53.1.148-170.1989 · Cited by 448

Show all 35 references

Research works printed but not linked: 3

Butanaev A. M., 1994, Hygromycin phosphotransferase gene as a dominant selective marker for transformation of Chlamydomonas reinhardtii, Mol. Biol., 28, 682
Cheney D. P., 1990, Economically Important Marine Plants of the Atlantic: Their Ecology and Cultivation, 15
Kurtzman A. L., 1991, Direct gene transfer and transient gene expression in a marine red alga using the biolistic method, J. Phycol., 27, 42

Sorted by citations

Items 101–200 of 305

Transcriptome and Gene Expression Analysis of an Oleaginous Diatom Under Different Salinity Conditions
Cheng, R., Feng, J., Zhang, B., Huang, Y. Y., Cheng, J., & Zhang, C. (2013) · BioEnergy Research · doi:10.1007/s12155-013-9360-1 · Cited by 67
Exploring Bioinorganic Pattern Formation in Diatoms. A Story of Polarized Trafficking
Zurzolo, C., & Bowler, C. (2001) · PLANT PHYSIOLOGY · doi:10.1104/pp.010709 · Cited by 67
Artificial miRNA inhibition of phosphoenolpyruvate carboxylase increases fatty acid production in a green microalga Chlamydomonas reinhardtii
Wang, C., Chen, X., Li, H., Wang, J., & Hu, Z. (2017) · Biotechnology for Biofuels · doi:10.1186/s13068-017-0779-z · Cited by 67
A stable and efficient nuclear transformation system for the diatom Chaetoceros gracilis
Ifuku, K., Yan, D., Miyahara, M., Inoue‐Kashino, N., Yamamoto, Y. Y., & Kashino, Y. (2014) · Photosynthesis Research · doi:10.1007/s11120-014-0048-y · Cited by 65
Discovery of genes for production of biofuels through transcriptome sequencing of Dunaliella parva
Shang, C., Bi, G., Yuan, Z., Wang, Z., Alam, M. A., & Xie, J. (2015) · Algal Research · doi:10.1016/j.algal.2015.12.012 · Cited by 64
Maneuvering the genetic and metabolic pathway for improving biofuel production in algae: Present status and future prospective
Banerjee, S., Banerjee, S., Ghosh, A. K., & Das, D. (2020) · Renewable and Sustainable Energy Reviews · doi:10.1016/j.rser.2020.110155 · Cited by 66
Genetic Transformation
Kroth, P. G. (2007) · Humana Press eBooks · doi:10.1007/978-1-59745-466-7_17 · Cited by 64
Semi-quantitative RT-PCR analysis of photoregulated gene expression in marine diatoms
Leblanc, C., Falciatore, A., Watanabe, M., & Bowler, C. (1999) · Plant Molecular Biology · doi:10.1023/a:1006256300969 · Cited by 64
Bioprospecting microalgae as potential sources of “Green Energy”—challenges and perspectives (Review)
Ratha, S. K., & Prasanna, R. (2012) · Applied Biochemistry and Microbiology · doi:10.1134/s000368381202010x · Cited by 65
Genetic engineering of microorganisms for biodiesel production
Lin, H., Wang, Q., Shen, Q., Zhan, J., & Zhao, Y. (2013) · Bioengineered · doi:10.4161/bioe.23114 · Cited by 63
Enhancing LC-PUFA production in Thalassiosira pseudonana by overexpressing the endogenous fatty acid elongase genes
Cook, O., & Hildebrand, M. (2015) · Journal of Applied Phycology · doi:10.1007/s10811-015-0617-2 · Cited by 63
Can Omics Approaches Improve Microalgal Biofuels under Abiotic Stress?
Salama, E., Govindwar, S. P., Khandare, R. V., Roh, H., Jeon, B., & Li, X. (2019) · Trends in Plant Science · doi:10.1016/j.tplants.2019.04.001 · Cited by 63
Response of Scenedesmus sp. to microwave treatment: Enhancement of lipid, exopolysaccharide and biomass production
Sivaramakrishnan, R., Suresh, S., Pugazhendhi, A., Pauline, J. M. N., & Incharoensakdi, A. (2020) · Bioresource Technology · doi:10.1016/j.biortech.2020.123562 · Cited by 60
Transforming kelp into a marine bioreactor
Qin, S., Jiang, P., & Tseng, C. (2005) · Trends in biotechnology · doi:10.1016/j.tibtech.2005.03.010 · Cited by 59
Genome editing in diatoms: achievements and goals
Kroth, P. G., Bones, A. M., Daboussi, F., Ferrante, M. I., Jaubert, M. J., Kolot, M., Nymark, M., Bártulos, C. R., Ritter, A., Russo, M. T., et al. (2018) · Plant Cell Reports · doi:10.1007/s00299-018-2334-1 · Cited by 59
Stable nuclear transformation of the diatom Chaetoceros sp.
Miyagawa‐Yamaguchi, A., Okami, T., Kira, N., Yamaguchi, H., Ohnishi, K., & Adachi, M. (2011) · Phycological Research · doi:10.1111/j.1440-1835.2011.00607.x · Cited by 58
Research note: High efficiency transformation of the diatom Phaeodactylum tricornutum with a promoter from the diatom Cylindrotheca fusiformis
Miyagawa‐Yamaguchi, A., Okami, T., Kira, N., Yamaguchi, H., Ohnishi, K., & Adachi, M. (2009) · Phycological Research · doi:10.1111/j.1440-1835.2009.00531.x · Cited by 57
GENETIC ENGINEERING OF EUKARYGTIC ALGAE: PROGRESS AND PROSPECTS
Stevens, D. R., & Purton, S. (1997) · Journal of Phycology · doi:10.1111/j.0022-3646.1997.00713.x · Cited by 57
Integrated analyses of transcriptome, proteome and fatty acid profilings of the oleaginous microalga Auxenochlorella protothecoides UTEX 2341 reveal differential reprogramming of fatty acid metabolism in response to low and high temperatures
Xing, G., Yuan, H., Yang, J., Li, J., Gao, Q., Li, W., & Wang, E. T. (2018) · Algal Research · doi:10.1016/j.algal.2018.04.028 · Cited by 55
Advantageous characteristics of the diatom Chaetoceros gracilis as a sustainable biofuel producer
Tokushima, H., Inoue‐Kashino, N., Nakazato, Y., Masuda, A., Ifuku, K., & Kashino, Y. (2016) · Biotechnology for Biofuels · doi:10.1186/s13068-016-0649-0 · Cited by 54
Algae Biotechnology – Green Cell-Factories on the Rise
Hallmann, A. (2015) · Current Biotechnology · doi:10.2174/2211550105666151107001338 · Cited by 58
Comparative Transcriptome Analysis Reveals a Potential Photosynthate Partitioning Mechanism between Lipid and Starch Biosynthetic Pathways in Green Microalgae
Chang, W.-C., Zheng, H.-Q., & Chen, C.-N. N. (2016) · Algal Research · doi:10.1016/j.algal.2016.03.007 · Cited by 53
Molecular Biology and the Biotechnological Potential of Diatoms
Kroth, P. G. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-75532-8_3 · Cited by 53
Latest Trends and Developments in Microalgae as Potential Source for Biofuels: The Case of Diatoms
Mourya, M., Khan, M. J., Ahirwar, A., Schoefs, B., Marchand, J., Rai, A., Varjani, S., Rajendran, K., Banu, J. R., & Vinayak, V. (2022) · Fuel · doi:10.1016/j.fuel.2021.122738 · Cited by 52
Recent Progress and Challenges in CRISPR-Cas9 Engineered Algae and Cyanobacteria
Patel, V. K., Das, A., Kumari, R., & Kajla, S. (2023) · Algal Research · doi:10.1016/j.algal.2023.103068 · Cited by 50
Species and Strain Selection
Borowitzka, M. A. (2013) · Algae for Biofuels and Energy · doi:10.1007/978-94-007-5479-9_4 · Cited by 50
Microalgal cultivation with waste streams and metabolic constraints to triacylglycerides accumulation for biofuel production
Ge, S., Champagne, P., Plaxton, W. C., Leite, G. B., & Marazzi, F. (2016) · Biofuels Bioproducts and Biorefining · doi:10.1002/bbb.1726 · Cited by 51
Engineering microalgae: transition from empirical design to programmable cells
Lu, Y., Zhang, X., Gu, X., Lin, H., & Melis, A. (2021) · Critical Reviews in Biotechnology · doi:10.1080/07388551.2021.1917507 · Cited by 52
Effect of overexpression of LPAAT and GPD1 on lipid synthesis and composition in green microalga Chlamydomonas reinhardtii
Wang, C., Li, Y., Lu, J., Deng, X. H., Li, H., & Hu, Z. (2017) · Journal of Applied Phycology · doi:10.1007/s10811-017-1349-2 · Cited by 50
Multiomics approaches and genetic engineering of metabolism for improved biorefinery and wastewater treatment in microalgae
Kuo, E. Y., Yang, R., Chin, Y. Y., Chien, Y., Chen, Y. C., Wei, C., Kao, L., Chang, Y., Li, Y., Chen, T., et al. (2022) · Biotechnology Journal · doi:10.1002/biot.202100603 · Cited by 51
Proteomic Analysis in Nitrogen-Deprived Isochrysis galbana during Lipid Accumulation
Song, P., Li, L., & Liu, J. (2013) · PLoS ONE · doi:10.1371/journal.pone.0082188 · Cited by 48
High‐value Recombinant Protein Production in Microalgae
Barrera, D. J., & Mayfield, S. P. (2013) · doi:10.1002/9781118567166.ch27 · Cited by 48
Microalgae as Feedstocks for Biodiesel Production
Liu, J., Huang, J., & Che, F. (2011) · InTech eBooks · doi:10.5772/25600 · Cited by 46
Free-standing microscale structures of nanocrystalline zirconia with biologically replicable three-dimensional shapes
Zhao, J., Gaddis, C. S., Cai, Y., & Sandhage, K. H. (2005) · Journal of materials research/Pratt's guide to venture capital sources · doi:10.1557/jmr.2005.0046 · Cited by 46
Phaeodactylum tricornutum : An established model species for diatom molecular research and an emerging chassis for algal synthetic biology
Russo, M. T., Rogato, A., Jaubert, M. J., Karas, B. J., & Falciatore, A. (2023) · Journal of Phycology · doi:10.1111/jpy.13400 · Cited by 45
Skeletonema marinoi as a new genetic model for marine chain-forming diatoms
Johansson, O., Töpel, M., Pinder, M. I. M., Kourtchenko, O., Blomberg, A., Godhe, A., & Clarke, A. K. (2019) · Scientific Reports · doi:10.1038/s41598-019-41085-5 · Cited by 45
Fast Fourier infrared spectroscopy to characterize the biochemical composition in diatoms
Kumar, V., Kashyap, M., Gautam, S., Shukla, P., Joshi, K. B., & Vinayak, V. (2018) · Journal of Biosciences · doi:10.1007/s12038-018-9792-z · Cited by 44
Characterization of marine diatom-infecting virus promoters in the model diatom Phaeodactylum tricornutum
Kadono, T., Miyagawa‐Yamaguchi, A., Kira, N., Tomaru, Y., Okami, T., Yoshimatsu, T., Hou, L., Ohama, T., Fukunaga, K., Okauchi, M., et al. (2015) · Scientific Reports · doi:10.1038/srep18708 · Cited by 44
Recent breakthroughs in integrated biomolecular and biotechnological approaches for enhanced lipid and carotenoid production from microalgae
Ahmad, A., BANAT, F. A., AlSafar, H. S., & Hasan, S. W. (2022) · Phytochemistry Reviews · doi:10.1007/s11101-022-09804-5 · Cited by 43
Rapid induction of GFP expression by the nitrate reductase promoter in the diatomPhaeodactylum tricornutum
Chu, L., Ewe, D., Bártulos, C. R., Kroth, P. G., & Gruber, A. (2016) · PeerJ · doi:10.7717/peerj.2344 · Cited by 43
Innovations in improving lipid production: Algal chemical genetics
Wase, N. V., Black, P., & Dirusso, C. (2018) · Progress in Lipid Research · doi:10.1016/j.plipres.2018.07.001 · Cited by 43
An intimate view into the silica deposition vesicles of diatoms
Heintze, C., Formánek, P., Pohl, D., Hauptstein, J., Rellinghaus, B., & Kröger, N. (2020) · BMC Materials · doi:10.1186/s42833-020-00017-8 · Cited by 43
Transcriptome sequencing, annotation and expression analysis of Nannochloropsis sp. at different growth phases
Zheng, M., Tian, J., Yang, G., Zheng, L., Chen, G., Chen, J., & Wang, B. (2013) · Gene · doi:10.1016/j.gene.2013.04.005 · Cited by 41
Expanding the toolbox for cryopreservation of marine and freshwater diatoms
Stock, W., Pinseel, E., Decker, S. D., Sefbom, J., Blommaert, L., Chepurnova, O., Sabbe, K., & Vyverman, W. (2018) · Scientific Reports · doi:10.1038/s41598-018-22460-0 · Cited by 44
Microalgae to biodiesel - Review of recent progress
Wood, D. A. (2021) · Bioresource Technology Reports · doi:10.1016/j.biteb.2021.100665 · Cited by 42
The past, present and future of algal continuous cultures in basic research and commercial applications
Henley, W. J. (2019) · Algal Research · doi:10.1016/j.algal.2019.101636 · Cited by 39
On Light and Diatoms: A Photonics and Photobiology Review
Ghobara, M., Ghobara, M., Mazumder, N., Vinayak, V., Reissig, L., Gebeshuber, I. C., Tiffany, M. A., Gordon, R., & Gordon, R. (2019) · Wiley eBooks · doi:10.1002/9781119370741.ch7 · Cited by 46
Phylogenomic Study of Lipid Genes Involved in Microalgal Biofuel Production—Candidate Gene Mining and Metabolic Pathway Analyses
Misra, N., Panda, P. K., Parida, B. K., & Mishra, B. K. (2012) · Evolutionary Bioinformatics · doi:10.4137/ebo.s10159 · Cited by 38
Way forward to achieve sustainable and cost-effective biofuel production from microalgae: a review
Misra, N., Panda, P. K., Parida, B. K., & Mishra, B. K. (2016) · International Journal of Environmental Science and Technology · doi:10.1007/s13762-016-1020-5 · Cited by 40
Development of gene expression system in a marine diatom using viral promoters of a wide variety of origin
Sakaue, K., Harada, H., & Matsuda, Y. (2008) · Physiologia Plantarum · doi:10.1111/j.1399-3054.2008.01089.x · Cited by 38
Potential Roles for Diatomists in Nanotechnology
Gordon, R., & Parkinson, J. (2005) · Journal of Nanoscience and Nanotechnology · doi:10.1166/jnn.2005.002 · Cited by 38
Establishment of Genetic Transformation in the Sexually Reproducing Diatoms Pseudo-nitzschia multistriata and Pseudo-nitzschia arenysensis and Inheritance of the Transgene
Sabatino, V., Russo, M. T., Patil, S., d’Ippolito, G., Fontana, A., & Ferrante, M. I. (2015) · Marine Biotechnology · doi:10.1007/s10126-015-9633-0 · Cited by 40
Alkaline phosphatase promoter as an efficient driving element for exogenic recombinant in the marine diatom Phaeodactylum tricornutum
Lin, H.-Y., Yen, S.-C., Kuo, P.-C., Chung, C.-Y., Yeh, K.-L., Huang, C.-H., Chang, J., & Lin, H. ‐. (2017) · Algal Research · doi:10.1016/j.algal.2017.01.007 · Cited by 35
Diatom plastids: Secondary endocytobiosis, plastid genome and protein import
Kroth, P. G., & Strotmann, H. (1999) · Physiologia Plantarum · doi:10.1034/j.1399-3054.1999.100118.x · Cited by 37
Porphyra monospore system (Bangiales, Rhodophyta): A model for the developmental biology of marine plants
Kitade, Y., Taguchi, G., Shin, J., & Saga, N. (1998) · Phycological Research · doi:10.1111/j.1440-1835.1998.tb00092.x · Cited by 34
Identification of the UMP Synthase Gene by Establishment of Uracil Auxotrophic Mutants and the Phenotypic Complementation System in the Marine DiatomPhaeodactylum tricornutum
Sakaguchi, T., Nakajima, K., & Matsuda, Y. (2011) · PLANT PHYSIOLOGY · doi:10.1104/pp.110.169631 · Cited by 34
Genome analysis and its significance in four unicellular algae, Cyanidioshyzon merolae, Ostreococcus tauri, Chlamydomonas reinhardtii, and Thalassiosira pseudonana
Misumi, O., Yoshida, Y., Nishida, K., Fujiwara, T., Sakajiri, T., Hirooka, S., Nishimura, Y., & Kuroiwa, T. (2007) · Journal of Plant Research · doi:10.1007/s10265-007-0133-9 · Cited by 34
Functional characterization of isolated plastids from two marine diatoms
Wittpoth, C., Kroth, P. G., Weyrauch, K., Kowallik, K. V., & Strotmann, H. (1998) · Planta · doi:10.1007/s004250050376 · Cited by 34
Immunological and molecular probes to detect phytoplankton responses to environmental stress in nature
Roche, J. L., McKay, R. M. L., & Boyd, P. W. (1999) · Springer eBooks · doi:10.1007/978-94-011-4201-4_13 · Cited by 35
Screening and transcriptomic analysis of Crypthecodinium cohnii mutants with high growth and lipid content using the acetyl-CoA carboxylase inhibitor sethoxydim
Liu, J., Pei, G., Diao, J., Chen, Z., Liu, L., Chen, L., & Zhang, W. (2017) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-017-8397-z · Cited by 33
Diatoms’ Breakthroughs in Biotechnology: Phaeodactylum tricornutum as a Model for Producing High-Added Value Molecules
Dhaouadi, F., Awwad, F., Diamond, A., & Desgagné‐Penix, I. (2020) · American Journal of Plant Sciences · doi:10.4236/ajps.2020.1110118 · Cited by 33
Marine Microalgae
Matsunaga, T., Takeyama, H., Miyashita, H., & Yokouchi, H. (2005) · Advances in biochemical engineering, biotechnology · doi:10.1007/b135784 · Cited by 34
Transformation techniques for metabolic engineering of diatoms and haptophytes: current state and prospects
Velmurugan, N., & Deka, D. (2018) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-018-8925-5 · Cited by 32
In the Grip of Algal Genomics
Grossman, A. R. (2008) · Advances in experimental medicine and biology · doi:10.1007/978-0-387-75532-8_6 · Cited by 32
TRANSIENT TRANSFORMATION OF A CHLORARACHNIOPHYTE ALGA, LOTHARELLA AMOEBIFORMIS (CHLORARACHNIOPHYCEAE), WITH uidA AND egfp REPORTER GENES 1
Hirakawa, Y., Kofuji, R., & Ishida, K. (2008) · Journal of Phycology · doi:10.1111/j.1529-8817.2008.00513.x · Cited by 32
Microalgal Biotechnology
Durvasula, R. V., Rao, D. V. S., & Rao, V. S. H. (2013) · CRC Press eBooks · doi:10.1201/b14920-14 · Cited by 31
Establishing Oleaginous Microalgae Research Models for Consolidated Bioprocessing of Solar Energy
Wang, D., Lu, Y., Huang, H., & Xu, J. (2011) · Advances in biochemical engineering, biotechnology · doi:10.1007/10_2011_122 · Cited by 30
Expression of Histophilus somni IbpA DR2 protective antigen in the diatom Thalassiosira pseudonana
Davis, A. K., Crum, L. T., Corbeil, L. B., & Hildebrand, M. (2017) · Applied Microbiology and Biotechnology · doi:10.1007/s00253-017-8267-8 · Cited by 30
Stable nuclear transformation of Pandorina morum
Lerche, K., & Hallmann, A. (2014) · BMC Biotechnology · doi:10.1186/1472-6750-14-65 · Cited by 30
Transgenic microalgae as bioreactors
Liang, Z., Liang, M., & Jiang, J. (2019) · Critical Reviews in Food Science and Nutrition · doi:10.1080/10408398.2019.1680525 · Cited by 28
Microalgae and Cyanobacteria as Green Molecular Factories: Tools and Perspectives
Urtubia, H. O., Betanzo, L. B., & Vásquez, M. (2016) · InTech eBooks · doi:10.5772/63006 · Cited by 29
Toward an understanding of lipid and starch accumulation in microalgae: A proteomic study of Neochloris oleoabundans cultivated under N-limited heterotrophic conditions
Morales‐Sánchez, D., Kyndt, J. A., Ogden, K. L., & Martı́nez, A. (2016) · Algal Research · doi:10.1016/j.algal.2016.09.006 · Cited by 28
Transcriptome analysis revealed the dynamic oil accumulation in Symplocos paniculata fruit
Liu, Q., Sun, Y., Chen, J., Li, P., Li, C., Niu, G., & Jiang, L. (2016) · BMC Genomics · doi:10.1186/s12864-016-3275-0 · Cited by 28
The Combination of RNA and Protein Profiling Reveals the Response to Nitrogen Depletion in Thalassiosira pseudonana
Jian, J., Zeng, D., Wei, W., Lin, H., Li, P., & Liu, W. (2017) · Scientific Reports · doi:10.1038/s41598-017-09546-x · Cited by 29
Diatomics: Toward Diatom Functional Genomics
Montsant, A., Maheswari, U., Bowler, C., & Lopez, P. J. (2005) · Journal of Nanoscience and Nanotechnology · doi:10.1166/jnn.2005.003 · Cited by 28
Advanced biotechnology in biorefinery: a new insight into municipal waste management to the production of high-value products
Haddadi, M. H., Aiyelabegan, H. T., & Negahdari, B. (2017) · International Journal of Environmental Science and Technology · doi:10.1007/s13762-017-1424-x · Cited by 27
New paradigm in diatom omics and genetic manipulation
Bhattacharjya, R., Tiwari, A., Marella, T. K., Bansal, H., & Srivastava, S. (2021) · Bioresource Technology · doi:10.1016/j.biortech.2021.124708 · Cited by 26
Biofuel production from microalgae and process enhancement by metabolic engineering and ultrasound
Makarem, M. A., Moravvej, Z., Rahimpour, M. R., & Vakylabad, A. B. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-821601-9.00008-x · Cited by 26
A method for genetic transformation of Botryococcus braunii using a cellulase pretreatment
Berrios, H., Zapata, M., & Rivas, M. (2015) · Journal of Applied Phycology · doi:10.1007/s10811-015-0596-3 · Cited by 25
Nuclear transformation of the diatom Phaeodactylum tricornutum using PCR-amplified DNA fragments by microparticle bombardment
Kira, N., Ohnishi, K., Miyagawa‐Yamaguchi, A., Kadono, T., & Adachi, M. (2015) · Marine Genomics · doi:10.1016/j.margen.2015.12.004 · Cited by 25
Surface sensing and stress-signalling inUlvaand fouling diatoms – potential targets for antifouling: a review
Thompson, S., & Coates, J. C. (2017) · Biofouling · doi:10.1080/08927014.2017.1319473 · Cited by 24
Genetic Engineering to Improve Algal Biofuels Production
Rasala, B. A., Gimpel, J. A., Tran, M., Hannon, M. J., Miyake-Stoner, S. J., Specht, E. A., & Mayfield, S. P. (2012) · Springer eBooks · doi:10.1007/978-94-007-5479-9_6 · Cited by 25
Recent Advances and Future Prospects of Microalgal Lipid Biotechnology
Ravindran, B., Kurade, M. B., Kabra, A. N., Jeon, B., & Gupta, S. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-51010-1_1 · Cited by 23
Structure and Regulation of Algal Light-Harvesting Complex Genes
Durnford, D. G. (2003) · Advances in photosynthesis and respiration · doi:10.1007/978-94-007-1038-2_4 · Cited by 23
Les microalgues
Cadoret, J., Bardor, M., Lerouge, P., Cabigliera, M., Henríquez, V., & Carlier, A. (2008) · médecine/sciences · doi:10.1051/medsci/2008244375 · Cited by 22
Genetic Engineering for Microalgae Strain Improvement in Relation to Biocrude Production Systems
Stephens, E., Wolf, J., Oey, M., Zhang, E., Hankamer, B. D., & Ross, I. L. (2015) · Biofuel and biorefinery technologies · doi:10.1007/978-3-319-16640-7_11 · Cited by 23
Algae: An Alternative to the Higher Plant System in Gene Farming
Griesbeck, C., & Kirchmayr, A. (2011) · Springer eBooks · doi:10.1007/978-94-007-2217-0_6 · Cited by 21
Current Status and Perspective on the Use of Viral-Based Vectors in Eukaryotic Microalgae
Bolaños−Martínez, O. C., Mahendran, G., Rosales‐Mendoza, S., & Vimolmangkang, S. (2022) · Marine Drugs · doi:10.3390/md20070434 · Cited by 21
Algae as a source of renewable energy: opportunities, challenges, and recent developments
Hussain, J., & Rittmann, B. E. (2023) · Sustainable Energy & Fuels · doi:10.1039/d2se01599d · Cited by 22
Development of a silicon limitation inducible expression system for recombinant protein production in the centric diatoms Thalassiosira pseudonana and Cyclotella cryptica
Shrestha, R. P., & Hildebrand, M. (2017) · Microbial Cell Factories · doi:10.1186/s12934-017-0760-3 · Cited by 20
Random mutagenesis and precise gene editing technologies: applications in algal crop improvement and functional genomics
Gan, S. Y., & Maggs, C. A. (2017) · European Journal of Phycology · doi:10.1080/09670262.2017.1358827 · Cited by 20
Exploiting Microalgae and Macroalgae for Production of Biofuels and Biosequestration of Carbon Dioxide—A Review
Gautam, K., Pareek, A., & Sharma, D. K. (2014) · International Journal of Green Energy · doi:10.1080/15435075.2014.893239 · Cited by 20
Green Alga (Chlamydomonas reinhardtii)
Rajam, M. V., & Kumar, S. V. (2006) · Humana Press eBooks · doi:10.1385/1-59745-131-2:421 · Cited by 20
Current Advances in Seaweed Transformation
Mikami, K. (2013) · InTech eBooks · doi:10.5772/52978 · Cited by 19
Relationship between acyl-lipid and sterol metabolisms in diatoms
Maréchal, É., & Lupette, J. (2019) · Biochimie · doi:10.1016/j.biochi.2019.07.005 · Cited by 19
Advances in Biochemical Engineering Biotechnology
Zeng, P.-T., Scheper, T. H., Hu, S., & Kasper, C. (2012) · British Library eBooks · Cited by 19
Genetic engineering in diatoms: advances and prospects
Li, Y., Deng, L., Walker, E. J. L., Karas, B. J., & Möck, T. (2025) · The Plant Journal · doi:10.1111/tpj.70102 · Cited by 19
A review on unit operations, challenges, opportunities, and strategies to improve algal based biodiesel and biorefinery
Kumar, L., Mohan, L., Anand, R., Joshi, V., Chugh, M., & Bharadvaja, N. (2022) · Frontiers in Chemical Engineering · doi:10.3389/fceng.2022.998289 · Cited by 20
The upstream regulatory sequence of the light harvesting complex Lhcf2 gene of the marine diatom Phaeodactylum tricornutum enhances transcription in an orientation- and distance-independent fashion
Russo, M. T., Annunziata, R., Sanges, R., Ferrante, M. I., & Falciatore, A. (2015) · Marine Genomics · doi:10.1016/j.margen.2015.06.010 · Cited by 17
Promoter Trapping in Microalgae Using the Antibiotic Paromomycin as Selective Agent
Vilà, M., Díaz‐Santos, E., de la Vega, M., Rodrı́guez, H., Vargas, Á., & León, R. (2012) · Marine Drugs · doi:10.3390/md10122749 · Cited by 18

Authors: Dunahay, T. G., Jarvis, E. E., & Roessler, P. G.
Affiliations: National Laboratory of the Rockies (US)
Venue: Journal of Phycology
Publisher: Wiley
Published: 1995-12
Volume: 31
Issue: 6
Pages: 1004-1012
ISSN: 0022-3646 (ISSN-L)
1529-8817
DOI: 10.1111/j.0022-3646.1995.01004.x
OpenAlex: W2062892053
Cited by: 306
References: 35
Citations by year: 2026: 2 · 2025: 5 · 2024: 7 · 2023: 11 · 2022: 14 · 2021: 12 · 2020: 8 · 2019: 20 · 2018: 12 · 2017: 27 · 2016: 20 · 2015: 20 · 2014: 17 · 2013: 17 · 2012: 19
FWCI: 3.82
Type: journal article
Language: en
Open access: closed
Licence: onlinelibrary.wiley.com/termsAndConditions#vor (vor, 4593 d)
Locations: Journal of Phycology (publishedVersion)
Topics: Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Diatoms and Algae Research
Life Sciences › Agricultural and Biological Sciences › Plant Science › Plant tissue culture and regeneration
Life Sciences › Agricultural and Biological Sciences › Ecology, Evolution, Behavior and Systematics › Protist diversity and phylogeny
Keywords: Cyclotella cryptica, neomycin phosphotransferase II, plasmid vectors, particle bombardment, G418 selection, tandem repeats, foreign DNA integration

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

GENETIC TRANSFORMATION OF THE DIATOMS CYCLOTELLA CRYPTICA AND NAVICULA SAPROPHILA

Abstract

Overview

Integrity signals

Verification

Claims the paper makes

Claims other papers make about this one

Citations

Cites

Cited by

Related

Metadata

Record

About these checks