New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. / Andersen, J B; Sternberg, C; Poulsen, L K; Bjorn, S P; Givskov, M; Molin, Søren.

In: Applied and Environmental Microbiology, Vol. 64, No. 6, 1998, p. 2240-6.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Andersen, JB, Sternberg, C, Poulsen, LK, Bjorn, SP, Givskov, M & Molin, S 1998, 'New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria', Applied and Environmental Microbiology, vol. 64, no. 6, pp. 2240-6.

APA

Andersen, J. B., Sternberg, C., Poulsen, L. K., Bjorn, S. P., Givskov, M., & Molin, S. (1998). New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Applied and Environmental Microbiology, 64(6), 2240-6.

Vancouver

Andersen JB, Sternberg C, Poulsen LK, Bjorn SP, Givskov M, Molin S. New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. Applied and Environmental Microbiology. 1998;64(6):2240-6.

Author

Andersen, J B ; Sternberg, C ; Poulsen, L K ; Bjorn, S P ; Givskov, M ; Molin, Søren. / New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria. In: Applied and Environmental Microbiology. 1998 ; Vol. 64, No. 6. pp. 2240-6.

Bibtex

@article{194bdbb0a862444189b062e05b30990b,
title = "New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria",
abstract = "Use of the green fluorescent protein (Gfp) from the jellyfish Aequorea victoria is a powerful method for nondestructive in situ monitoring, since expression of green fluorescence does not require any substrate addition. To expand the use of Gfp as a reporter protein, new variants have been constructed by the addition of short peptide sequences to the C-terminal end of intact Gfp. This rendered the Gfp susceptible to the action of indigenous housekeeping proteases, resulting in protein variants with half-lives ranging from 40 min to a few hours when synthesized in Escherichia coli and Pseudomonas putida. The new Gfp variants should be useful for in situ studies of temporal gene expression.",
author = "Andersen, {J B} and C Sternberg and Poulsen, {L K} and Bjorn, {S P} and M Givskov and S{\o}ren Molin",
year = "1998",
language = "English",
volume = "64",
pages = "2240--6",
journal = "Applied and Environmental Microbiology",
issn = "0099-2240",
publisher = "American Society for Microbiology",
number = "6",

}

RIS

TY - JOUR

T1 - New unstable variants of green fluorescent protein for studies of transient gene expression in bacteria

AU - Andersen, J B

AU - Sternberg, C

AU - Poulsen, L K

AU - Bjorn, S P

AU - Givskov, M

AU - Molin, Søren

PY - 1998

Y1 - 1998

N2 - Use of the green fluorescent protein (Gfp) from the jellyfish Aequorea victoria is a powerful method for nondestructive in situ monitoring, since expression of green fluorescence does not require any substrate addition. To expand the use of Gfp as a reporter protein, new variants have been constructed by the addition of short peptide sequences to the C-terminal end of intact Gfp. This rendered the Gfp susceptible to the action of indigenous housekeeping proteases, resulting in protein variants with half-lives ranging from 40 min to a few hours when synthesized in Escherichia coli and Pseudomonas putida. The new Gfp variants should be useful for in situ studies of temporal gene expression.

AB - Use of the green fluorescent protein (Gfp) from the jellyfish Aequorea victoria is a powerful method for nondestructive in situ monitoring, since expression of green fluorescence does not require any substrate addition. To expand the use of Gfp as a reporter protein, new variants have been constructed by the addition of short peptide sequences to the C-terminal end of intact Gfp. This rendered the Gfp susceptible to the action of indigenous housekeeping proteases, resulting in protein variants with half-lives ranging from 40 min to a few hours when synthesized in Escherichia coli and Pseudomonas putida. The new Gfp variants should be useful for in situ studies of temporal gene expression.

M3 - Journal article

C2 - 9603842

VL - 64

SP - 2240

EP - 2246

JO - Applied and Environmental Microbiology

JF - Applied and Environmental Microbiology

SN - 0099-2240

IS - 6

ER -

ID: 44308650