Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.
Size (kb): 8.900
Vector: pRB382 (plasmid)
Promoters: Promoter vegII (B. subtilis)
Construction: pUB110, pBR322, lacZ, vegII
Construct size (kb): 8.900
Features: marker(s): ampR
promoter: vegII (B. subtilis)
reporter group: 'lacZ
terminator: To phage lambda
transcription terminator: rrnB
vector permitting visual detection of activity in colonies
Restriction digests of the clone give the following sizes (kb): BamHI--9.5; EcoRI/BglI--5.1, 2.2, 1.1, 0.8; BglI/BglII--3.5, 2.2, 2.0, 1.4.
The Bacillus subtilis promoter vegII initiates transcription in both B. subtilis and E. coli.
Structural stability of the plasmid in B. subtilis can be affected by high levels of protein production. Under these conditions, cell growth and stability may be improved by reducing the antibiotic concentration in the media.
May not be suitable for cloning very strong expression signals.
Translational fusion shuttle vector using 'lacZ as reporter. Also contains the vegII promoter. Useful for construction of fusion proteins.
Neo confers resistance to neomycin and kanamycin and ble confers resistance to bleomycin and phleomycin.
The 5' truncated 'lacZ gene, lacking transcriptional and translational initiation signals, is useful in both E. coli and in B. subtilis, since the endogenous beta-galactosidase level in B. subtilis is low.
Bruckner R. A series of shuttle vectors for Bacillus subtilis and Eschericia coli. Gene 122: 187-192, 1992. PubMed: 1452028