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Detection of recombinant human lactoferrin and lysozyme produced in a bitransgenic cow
Abstract
Lactoferrin and lysozyme are 2 glycoproteins with
great antimicrobial activity, being part of the nonspecific
defensive system of human milk, though their use
in commercial products is difficult because human milk
is a limited source. Therefore, many investigations have
been carried out to produce those proteins in biological
systems, such as bacteria, yeasts, or plants. Mammals
seem to be more suitable as expression systems for
human proteins,
[ver mas...]
Lactoferrin and lysozyme are 2 glycoproteins with
great antimicrobial activity, being part of the nonspecific
defensive system of human milk, though their use
in commercial products is difficult because human milk
is a limited source. Therefore, many investigations have
been carried out to produce those proteins in biological
systems, such as bacteria, yeasts, or plants. Mammals
seem to be more suitable as expression systems for
human proteins, however, especially for those that are
glycosylated. In the present study, we developed a bicistronic
commercial vector containing a goat β-casein
promoter and an internal ribosome entry site fragment
between the human lactoferrin and human lysozyme
genes to allow the introduction of both genes into bovine
adult fibroblasts in a single transfection. Embryos
were obtained by somatic cell nuclear transfer, and,
after 6 transferences to recipients, 3 pregnancies and 1
viable bitransgenic calf were obtained. The presence of
the vector was confirmed by fluorescent in situ hybridization
of skin cells. At 13 mo of life and after artificial
induction of lactation, both recombinant proteins were
found in the colostrum and milk of the bitransgenic
calf. Human lactoferrin concentration in the colostrum
was 0.0098 mg/mL and that in milk was 0.011 mg/mL;
human lysozyme concentration in the colostrum was
0.0022 mg/mL and that in milk was 0.0024 mg/mL. The
molar concentration of both human proteins revealed
no differences in protein production of the internal ribosome
entry site upstream and downstream protein.
The enzymatic activity of lysozyme in the transgenic
milk was comparable to that of human milk, being 6
and 10 times higher than that of bovine lysozyme presentin milk. This work represents an important step to
obtain multiple proteins or enhance single protein production
by using animal pharming and fewer regulatory
and antibiotic-resistant foreign sequences, allowing the
design of humanized milk with added biological value
for newborn nutrition and development. Transgenic
animals can offer a unique opportunity to the dairy industry,
providing starting materials suitable to develop
specific products with high added value.
Key words: bitransgenic cow, human lactoferrin,
ELISA, human lysozyme.
[Cerrar]
Author
Kaiser, German Gustavo;
Mucci, Nicolas Crescencio;
Gonzalez, Vega;
Sánchez, Lourdes;
Parrón, José Antonio;
Pérez, María Dolores;
Calvo, Miguel;
Aller Atucha, Juan Florencio;
Hozbor, Federico Andres;
Mutto, Adrián Angel;
Fuente
Journal of dairy science 100 (3) : 1605–1617. (March 2017)
Date
2017-03
ISSN
0022-0302
Formato
pdf
Tipo de documento
artículo
Palabras Claves
Derechos de acceso
Abierto
Excepto donde se diga explicitamente, este item se publica bajo la siguiente descripción: Creative Commons Attribution-NonCommercial-ShareAlike 2.5 Unported (CC BY-NC-SA 2.5)