Current approaches to genetic modification of marine bacteria and considerations for improved transformation efficiency

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Natural Transformation in a Classical-Biotype Vibrio cholerae Strain

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Type I restriction-modification system and its resistance in electroporation efficiency in Flavobacterium columnare

Li, N., Zhang, L., Zhang, J., Liu, Z. X., Huang, B., Zhang, S. H., & Nie, P. (2012) · Veterinary Microbiology · doi:10.1016/j.vetmic.2012.04.045 · Cited by 5 · see citing works

Improved Method for Transformation of Vibrio vulnificus by Electroporation

Jayakumar, J. M., Shapiro, O. H., & Almagro‐Moreno, S. (2020) · Current Protocols in Microbiology · doi:10.1002/cpmc.106 · Cited by 5 · see citing works

A modular plasmid toolkit applied in marine Proteobacteria reveals functional insights during bacteria-stimulated metamorphosisPreprint

Alker, A. T., Aspiras, A. E., Dunbar, T. L., Farrell, M. V., Fedoriouk, A., Jones, J. E., Mikhail, S. R., Salcedo, G. Y., Moore, B. S., & Shikuma, N. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.31.526474 · Cited by 5 · see citing works

Beyond the ABCs—Discovery of Three New Plasmid Types in Rhodobacterales (RepQ, RepY, RepW)

Freese, H. M., Ringel, V., Overmann, J., & Petersen, J. (2022) · Microorganisms · doi:10.3390/microorganisms10040738 · Cited by 3 · see citing works

Engineering the highly productive cyanobacterium Synechococcus sp. PCC 11901Preprint

Victoria, A. J., Selão, T. T., Moreno-Cabezuelo, J. Á., Mills, L. A., Gale, G. A. R., Lea‐Smith, D. J., & McCormick, A. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.08.04.552009 · Cited by 3 · see citing works

Salinity-dependent copy number change of endogenous plasmids in Synechococcus sp. strain PCC 7002

Yano, S.-I., Kawata, Y., & Kojima, H. (1995) · Current Microbiology · doi:10.1007/bf00294699 · Cited by 2 · see citing works

Recombineering in Staphylococcus aureus

Penewit, K. M., & Salipante, S. J. (2022) · Methods in molecular biology · doi:10.1007/978-1-0716-2233-9_10 · Cited by 1 · see citing works

Adaptive laboratory evolution and mechanisms of salt tolerance in Lactiplantibacillus plantarum

Han, J., Sun, Z., Chen, Y., Guo, J., Zhang, S., & Ji, C. (2024) · Food Bioscience · doi:10.1016/j.fbio.2024.105811 · Cited by 17 · see citing works

Engineered Marine Biofilms for Ocean Environment Monitoring

Nevot, G., Cros, M. P., Toloza, L., Sanz, N. C., Artigues-Lleixà, M., Aguilera, L., & Güell, M. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00192 · Cited by 5 · see citing works

Harnessing the Endogenous Type I–F CRISPR/Cas System for Efficient Genome Engineering and Gene Repression in Pseudomonas chlororaphis LX24

Nie, Y., Yue, S., Huang, P., Hu, D., Xu, Z., Aguilar-Vera, A., Utrilla, J., Zhang, X., & Hu, H. (2025) · ACS Synthetic Biology · doi:10.1021/acssynbio.5c00371 · Cited by 2 · see citing works

Cyanobacteria as a Photosynthetic Chassis for Metabolic Pathway Engineering with Heterologous Gene Expression

Walshe, J., & Saha, S. K. (2026) · Current Issues in Molecular Biology · doi:10.3390/cimb48060638 · Cited by 1 · see citing works

Genetic Changes, Epigenetic Modifications and Antibiotic Resistance Caused by Bacterial Infection

Hashemzadeh, M., & Dezfuli, A. A. Z. (2024) · Genetics. · doi:10.5772/intechopen.1006623 · Cited by 1 · see citing works

Marine-based Drug Candidates: Cutting-edge Innovations and Strategies in Modern Drug Discovery

Kalasariya, H. S., Maya-Ramírez, C. E., Cotas, J., & Pereira, L. (2025) · Royal Society of Chemistry eBooks · doi:10.1039/9781837676989-00148

Conjugative serine recombinase engineering enables genome integration in transformation-resistant bacteria and bioproduction pathway prototypingPreprint

Guzman, M. S., Kiattisewee, C., Robert, A. M., Comes, J. S., Cardiff, R. A. L., Scott, A., Cook, M., Burbano, D. A., Anastasakis, S., Grube, S., et al. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.04.17.717921

The development of RPA–CRISPR/Cas12a assay for the detection of Pseudomonas plecoglossicida

Li, Y., Du, H., Chen, J., Xiao, J., Ma, Y., Zhang, Y., & Wang, Q. (2026) · FEMS Microbiology Letters · doi:10.1093/femsle/fnag067

Methods for the genetic manipulation of marine bacteria

Zeaiter, Z., Mapelli, F., Crotti, E., & Borin, S. (2018) · Electronic Journal of Biotechnology · doi:10.1016/j.ejbt.2018.03.003 · Cited by 34 · see citing works

A modular plasmid toolkit applied in marine bacteria reveals functional insights during bacteria-stimulated metamorphosis

Alker, A. T., Farrell, M. V., Aspiras, A. E., Dunbar, T. L., Fedoriouk, A., Jones, J. E., Mikhail, S. R., Salcedo, G. Y., Moore, B. S., & Shikuma, N. J. (2023) · mBio · doi:10.1128/mbio.01502-23 · Cited by 17 · see citing works

A modular plasmid toolkit applied in marine Proteobacteria reveals functional insights during bacteria-stimulated metamorphosisPreprint

Alker, A. T., Aspiras, A. E., Dunbar, T. L., Farrell, M. V., Fedoriouk, A., Jones, J. E., Mikhail, S. R., Salcedo, G. Y., Moore, B. S., & Shikuma, N. J. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.31.526474 · Cited by 5 · see citing works

Electroporation - mediated transformation protocol for marine isolated bacteria v1Preprint

Arnli, W., Bjerg, J., & Bernstein, H. C. (2025) · doi:10.17504/protocols.io.rm7vzqwmrvx1/v1

Method for the facile transformation of marine purple photosynthetic bacteria using chemically competent cells

Higuchi‐Takeuchi, M., Morisaki, K., & Numata, K. (2019) · MicrobiologyOpen · doi:10.1002/mbo3.953 · Cited by 15 · see citing works