Copy number determination, expression analysis of genes potentially involved in replication, and stability assays of pAL1-the linear megaplasmid of Arthrobacter nitroguajacolicus Ru61a

Wagenknecht M, Meinhardt F

Forschungsartikel (Zeitschrift) | Peer reviewed

Zusammenfassung

pAL1 of the actinomycete Arthrobacter nitroguajacolicus Ru61a, a 113-kb catabolic linear megaplasmid of the invertron-type, enables its host to utilize quinaldine (or 4-hydroxyquinaldine) as the sole carbon and energy source. Comparative Southern hybridization and quantitative real-time PCR analyses revealed copy numbers of two for cells grown in minimal medium supplemented with 4-hydroxyquinaldine and four for cells cultivated in Luria-Bertani medium. However, medium-dependent differences in the expression levels of genes potentially involved in plasmid replication were not seen. As replication and maintenance of invertrons may depend on single-stranded DNA-binding proteins (SSBs), ORF39, the gene product of which displaying similarities to SSBs, was knocked out. However, structural stability and replication of pAL1 was not influenced. When plasmid maintenance of LB-grown wild-type cells was assessed, it was seen that after approx. 200 generations almost 80% of the cells were devoid of plasmid, indicating segregational instability of pAL1. (C) 2010 Elsevier GmbH. All rights reserved.

Details zur Publikation

FachzeitschriftMicrobiological Research
Jahrgang / Bandnr. / Volume166
Ausgabe / Heftnr. / Issue1
Seitenbereich14-26
StatusVeröffentlicht
Veröffentlichungsjahr2011 (31.12.2011)
Sprache, in der die Publikation verfasst istEnglisch
StichwörterLinear plasmid Copy number Arthrobacter Quantitative real-time PCR complete nucleotide-sequence phi-29 dna-replication escherichia-coli streptomyces-lividans binding protein transcriptional analysis plasmid incompatibility bacteriophage prd1 terminal protein bacterial-growth

Autor*innen der Universität Münster

Meinhardt, Friedhelm

Projekte, aus denen die Publikation entstanden ist

Laufzeit: 01.04.2006 - 31.03.2009
Gefördert durch: DFG - Sachbeihilfe/Einzelförderung
Art des Projekts: Gefördertes Einzelprojekt