TU Darmstadt / ULB / TUbiblio

Transformation of Halobacterium halobium: development of vectors and investigation of gas vesicle synthesis.

Blaseio, U. ; Pfeifer, Felicitas (1990)
Transformation of Halobacterium halobium: development of vectors and investigation of gas vesicle synthesis.
In: Proceedings of the National Academy of Sciences of the United States of America, 87 (17)
Artikel, Bibliographie

Kurzbeschreibung (Abstract)

We developed vector plasmids for the transformation of Halobacterium halobium, using the replicon region from the halobacterial phage H or from the plasmid pHH1 together with a DNA fragment conferring resistance to mevinolin. H. halobium P03, a strain lacking pHH1 as well as the restriction endonuclease activity found in wild-type H. halobium, was used as the recipient strain. All H. halobium fragments tested for autonomous replication as well as the Haloferax volcanii vector pWL102 enabled stable plasmid maintenance in this strain. A frequent loss of all vectors (including pWL102) was observed in Hf. volcanii, where >90% of the mevinolin-resistant colonies obtained after transformation had lost the vector, presumably because of restriction endonuclease activity and concomitant recombination of the mevinolin resistance marker with the chromosome. The expression of gas vesicle-encoding genes (vac) was analyzed by using a 4.5-kilobase-pair (kbp) fragment containing the plasmid-encoded p-vac gene from H. halobium or an 11-kbp fragment containing the mc-vac chromosomal gene from Haloferax mediterranei for transformation experiments with H. halobium and Hf. volcanii. These experiments indicated that the mc-vac fragment contains all information necessary to synthesize gas vesicles, whereas in the case of the smaller p-vac fragment, complementation by other genes was required for a Vac+ phenotype.

Typ des Eintrags: Artikel
Erschienen: 1990
Autor(en): Blaseio, U. ; Pfeifer, Felicitas
Art des Eintrags: Bibliographie
Titel: Transformation of Halobacterium halobium: development of vectors and investigation of gas vesicle synthesis.
Sprache: Englisch
Publikationsjahr: 1990
Titel der Zeitschrift, Zeitung oder Schriftenreihe: Proceedings of the National Academy of Sciences of the United States of America
Jahrgang/Volume einer Zeitschrift: 87
(Heft-)Nummer: 17
Kurzbeschreibung (Abstract):

We developed vector plasmids for the transformation of Halobacterium halobium, using the replicon region from the halobacterial phage H or from the plasmid pHH1 together with a DNA fragment conferring resistance to mevinolin. H. halobium P03, a strain lacking pHH1 as well as the restriction endonuclease activity found in wild-type H. halobium, was used as the recipient strain. All H. halobium fragments tested for autonomous replication as well as the Haloferax volcanii vector pWL102 enabled stable plasmid maintenance in this strain. A frequent loss of all vectors (including pWL102) was observed in Hf. volcanii, where >90% of the mevinolin-resistant colonies obtained after transformation had lost the vector, presumably because of restriction endonuclease activity and concomitant recombination of the mevinolin resistance marker with the chromosome. The expression of gas vesicle-encoding genes (vac) was analyzed by using a 4.5-kilobase-pair (kbp) fragment containing the plasmid-encoded p-vac gene from H. halobium or an 11-kbp fragment containing the mc-vac chromosomal gene from Haloferax mediterranei for transformation experiments with H. halobium and Hf. volcanii. These experiments indicated that the mc-vac fragment contains all information necessary to synthesize gas vesicles, whereas in the case of the smaller p-vac fragment, complementation by other genes was required for a Vac+ phenotype.

Fachbereich(e)/-gebiet(e): 10 Fachbereich Biologie > Microbiology and Archaea
?? fb10_mikrobiologie ??
10 Fachbereich Biologie
Hinterlegungsdatum: 14 Feb 2011 10:59
Letzte Änderung: 05 Mär 2013 09:45
PPN:
Export:
Suche nach Titel in: TUfind oder in Google
Frage zum Eintrag Frage zum Eintrag

Optionen (nur für Redakteure)
Redaktionelle Details anzeigen Redaktionelle Details anzeigen