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

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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

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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.

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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

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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

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GENETIC TRANSFORMATION OF THE DIATOMS CYCLOTELLA CRYPTICA AND NAVICULA SAPROPHILA

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