Green fluorescent protein as a reporter for spatial and temporal gene expression in Streptomyces coelicolor A3(2)

Jongho Sun, Gabriella H. Kelemen, José Manuel Fernández-Abalos, Mervyn J. Bibb

Research output: Contribution to journalArticlepeer-review

198 Citations (Scopus)

Abstract

The enhanced green fluorescent protein (EGFP) gene is a modified version of the green fluorescent protein gene of the jellyfish Aequorea victoria with a codon usage that corresponds well to that found in many GC-rich streptomycete genes. Here the use of ECFP as a reporter for the analysis of spatially and temporally regulated gene expression in Streptomyces coelicolor A3(2) is demonstrated. The EGFP gene was inserted into plasmids that can replicate in Escherichia coli, greatly facilitating the construction of ECFP gene fusions. The plasmids can be transferred readily to S. coelicolor by conjugation, whereupon two of them (pIJ8630 and pIJ8660) integrate at the chromosomal attachment site for the temperate phage ∅C31. These vectors were used to analyse the spatial and temporal expression of sigF, which encodes a σ factor required for spore maturation, and of redD, a pathway-specific regulatory gene for the production of undecylprodigiosin, one of the four antibiotics made by S. coelicolor. While transcription of sigF appeared to be confined to developing and mature spore chains, transcription of redD occurred only in ageing substrate mycelium. A further plasmid derivative (pIJ8668) was made that lacks the ∅C31 attachment site, allowing the EGFP gene to be fused transcriptionally to genes of interest at their native chromosomal locations.

Original languageEnglish
Pages (from-to)2221-2227
Number of pages7
JournalMicrobiology
Volume145
Issue number9
DOIs
Publication statusPublished - 1 Sep 1999

Keywords

  • Green fluorescent protein (GFP)
  • redD
  • sigF
  • Streptomyces coelicolor A3(2)
  • tipAp

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