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Construction and characterization of shuttle vectors for succinic acid-producing rumen bacteria.


ABSTRACT: Shuttle vectors carrying the origins of replication that function in Escherichia coli and two capnophilic rumen bacteria, Mannheimia succiniciproducens and Actinobacillus succinogenes, were constructed. These vectors were found to be present at ca. 10 copies per cell. They were found to be stably maintained in rumen bacteria during the serial subcultures in the absence of antibiotic pressure for 216 generations. By optimizing the electroporation condition, the transformation efficiencies of 3.0 x 10(6) and 7.1 x 10(6) transformants/mug DNA were obtained with M. succiniciproducens and A. succinogenes, respectively. A 1.7-kb minimal replicon was identified that consists of the rep gene, four iterons, A+T-rich regions, and a dnaA box. It was found that the shuttle vector replicates via the theta mode, which was confirmed by sequence analysis and Southern hybridization. These shuttle vectors were found to be suitable as expression vectors as the homologous fumC gene encoding fumarase and the heterologous genes encoding green fluorescence protein and red fluorescence protein could be expressed successfully. Thus, the shuttle vectors developed in this study should be useful for genetic and metabolic engineering of succinic acid-producing rumen bacteria.

SUBMITTER: Jang YS 

PROVIDER: S-EPMC2042079 | biostudies-literature | 2007 Sep

REPOSITORIES: biostudies-literature

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Construction and characterization of shuttle vectors for succinic acid-producing rumen bacteria.

Jang Yu-Sin YS   Jung Young Ryul YR   Lee Sang Yup SY   Kim Ji Mahn JM   Lee Jeong Wook JW   Oh Doo-Byoung DB   Kang Hyun Ah HA   Kwon Ohsuk O   Jang Seh Hee SH   Song Hyohak H   Lee Sang Jun SJ   Kang Kyu Young KY  

Applied and environmental microbiology 20070706 17


Shuttle vectors carrying the origins of replication that function in Escherichia coli and two capnophilic rumen bacteria, Mannheimia succiniciproducens and Actinobacillus succinogenes, were constructed. These vectors were found to be present at ca. 10 copies per cell. They were found to be stably maintained in rumen bacteria during the serial subcultures in the absence of antibiotic pressure for 216 generations. By optimizing the electroporation condition, the transformation efficiencies of 3.0  ...[more]

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