Poster presentation
185
OBTAINING RECOMBINANT BACULOVIRUSES
IN Bac-to-Bac® PLATFORM
Sh.Sh. Khasanov, M.Sh. Shukurjonov, J.M. Abdurakhmanov, O.N. Ashirov,
F.B. Eshboev, S.A. Gaynazarova, S.A. Sasmakov, Sh.S. Azimova
S.Yu. Yunusov Institute of the Chemistry of Plant Substances Academy of sciences of the
Republic of Uzbekistan st. Mirzo-Ulugbek, 77, 100170 Tashkent
e-mail: genlab_icps@yahoo.com
Usually, for construction of recombinant baculoviruses for highly efficient
expression of a foreign gene the cDNA of this gene is ligated with plasmid DNA
containing a viral DNA fragment. Also, the target cDNA is inserted under the control of
a strong viral polyhedrin gene promoter [1]. To obtain a recombinant baculovirus the
insect cells are infected simultaneously with the recombinant
plasmid and wild-type
baculovirus. Recombination between homologous sequences of viral and plasmid DNA
leads to the replacement of the polyhedrin gene in wild-type viral DNA with plasmid
sequences containing foreign cDNA [2]. Today, these processes cause several
difficulties. We have chosen the relatively easy-to-use Bac-to-Bac® platform. The Bac-
to-Bac® Baculovirus Expression System provides a rapid
and efficient method to
generate recombinant baculoviruses. This method is based on site-specific transposition
of an expression cassette into a baculovirus shuttle vector (bacmid) propagated in
Escherichia coli.
In our experiments, we obtained a recombinant baculovirus (bacmid) using the
Escherichia coli
host strain DH10Bac™ and the pFastBac™
genetic construct
containing a baculovirus vector (bacmid) and a helper plasmid. We generated
recombinant baculoviruses using the MAX Efficiency® DH10Bac™ chemically
competent cells (Transform Aid Bacterial Transformation Kit).
The LB agar plates
containing 60 μg/ml kanamycin, 7 μg/ml gentamicin and 15 μg/ml tetracycline used to
select DH10Bac™ recombinant transformants. To verify the presence of gene of
interest in the recombinant bacmid the PCR assay is performed. The size of obtained
recombinant bacmid DNA is greater than 135 kb.
References:
1. BacPAK
Baculovirus Expression System User Manual. Cat. No. 631402
PT1260-1(072313), 2013. http://www.clontech.com
2. O′Reilly D.R., Miller L.K., Luckow V.A. Baculovirus Expression Vectors: A
Laboratory Manual.
Oxford University Press, 1994, 347 pp.
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