Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis

Expression of plasmid-encoded resistances in regenerating protoplasts of Bacillus subtilis occurs only after wall synthesis has been resumed. This is observed for protoplasts obtained from cells already containing plasmids (pC194, pT127, pK545) or for plasmid-bearing cells coming from a PEG-mediated...

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Publicado: 1988
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Acceso en línea:https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07692609_v139_n4_p403_SanchezRivas
http://hdl.handle.net/20.500.12110/paper_07692609_v139_n4_p403_SanchezRivas
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spelling paper:paper_07692609_v139_n4_p403_SanchezRivas2023-06-08T15:45:46Z Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis Bacillus subtilis, Plasmid, Protoplast Transformation, Gene expression, Cell wall regeneration bacillus subtilis bacterium transformation cell wall gene expression genetic engineering nonhuman plasmid priority journal protoplast Bacillus subtilis Cell Wall Culture Media Drug Resistance, Microbial Gene Expression Regulation Osmotic Pressure Protoplasts R Factors Support, Non-U.S. Gov't Transformation, Bacterial Expression of plasmid-encoded resistances in regenerating protoplasts of Bacillus subtilis occurs only after wall synthesis has been resumed. This is observed for protoplasts obtained from cells already containing plasmids (pC194, pT127, pK545) or for plasmid-bearing cells coming from a PEG-mediated transformation. Recovery of expression needs a 2-h incubation of protoplasts, previously washed to get rid of their lysozyme content, in rich hypertonic medium (SMMP). A longer incubation (24-h) results in the obtention of regenerants; however, most of them have lost their resistant phenotype in contrast to those obtained from the usual solid regeneration plates. This finding suggests either a high curing effect or some kind of gene inactivation phenomenon. Discussion is focused on the critical points that have to be considered when polyethylenglycol-mediated transformation of protoplasts is applied to recombinant DNA technology. © 1988. 1988 https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07692609_v139_n4_p403_SanchezRivas http://hdl.handle.net/20.500.12110/paper_07692609_v139_n4_p403_SanchezRivas
institution Universidad de Buenos Aires
institution_str I-28
repository_str R-134
collection Biblioteca Digital - Facultad de Ciencias Exactas y Naturales (UBA)
topic Bacillus subtilis, Plasmid, Protoplast
Transformation, Gene expression, Cell wall regeneration
bacillus subtilis
bacterium transformation
cell wall
gene expression
genetic engineering
nonhuman
plasmid
priority journal
protoplast
Bacillus subtilis
Cell Wall
Culture Media
Drug Resistance, Microbial
Gene Expression Regulation
Osmotic Pressure
Protoplasts
R Factors
Support, Non-U.S. Gov't
Transformation, Bacterial
spellingShingle Bacillus subtilis, Plasmid, Protoplast
Transformation, Gene expression, Cell wall regeneration
bacillus subtilis
bacterium transformation
cell wall
gene expression
genetic engineering
nonhuman
plasmid
priority journal
protoplast
Bacillus subtilis
Cell Wall
Culture Media
Drug Resistance, Microbial
Gene Expression Regulation
Osmotic Pressure
Protoplasts
R Factors
Support, Non-U.S. Gov't
Transformation, Bacterial
Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
topic_facet Bacillus subtilis, Plasmid, Protoplast
Transformation, Gene expression, Cell wall regeneration
bacillus subtilis
bacterium transformation
cell wall
gene expression
genetic engineering
nonhuman
plasmid
priority journal
protoplast
Bacillus subtilis
Cell Wall
Culture Media
Drug Resistance, Microbial
Gene Expression Regulation
Osmotic Pressure
Protoplasts
R Factors
Support, Non-U.S. Gov't
Transformation, Bacterial
description Expression of plasmid-encoded resistances in regenerating protoplasts of Bacillus subtilis occurs only after wall synthesis has been resumed. This is observed for protoplasts obtained from cells already containing plasmids (pC194, pT127, pK545) or for plasmid-bearing cells coming from a PEG-mediated transformation. Recovery of expression needs a 2-h incubation of protoplasts, previously washed to get rid of their lysozyme content, in rich hypertonic medium (SMMP). A longer incubation (24-h) results in the obtention of regenerants; however, most of them have lost their resistant phenotype in contrast to those obtained from the usual solid regeneration plates. This finding suggests either a high curing effect or some kind of gene inactivation phenomenon. Discussion is focused on the critical points that have to be considered when polyethylenglycol-mediated transformation of protoplasts is applied to recombinant DNA technology. © 1988.
title Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
title_short Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
title_full Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
title_fullStr Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
title_full_unstemmed Expression and maintenance of plasmid resistance in regenerating protoplasts of Bacillus subtilis
title_sort expression and maintenance of plasmid resistance in regenerating protoplasts of bacillus subtilis
publishDate 1988
url https://bibliotecadigital.exactas.uba.ar/collection/paper/document/paper_07692609_v139_n4_p403_SanchezRivas
http://hdl.handle.net/20.500.12110/paper_07692609_v139_n4_p403_SanchezRivas
_version_ 1768544645561712640