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Reproduction, Fertility and Development Reproduction, Fertility and Development Society
Vertebrate reproductive science and technology
RESEARCH ARTICLE

Plant protein hydrolysates (plant peptones) as substitutes for animal proteins in embryo culture medium

F. George A , D. Kerschen A , A. Van Nuffel A , J. F. Rees B and I. Donnay A C
+ Author Affiliations
- Author Affiliations

A Université catholique de Louvain, Institut des Sciences de la Vie, Unité des Sciences vétérinaires, Place Croix du Sud 5 Box 10, B-1348 Louvain-la-Neuve, Belgium.

B Université catholique de Louvain, Institut des Sciences de la Vie, Unité de Biologie Animale, Place Croix du Sud 5 Box 2, B-1348 Louvain-la-Neuve, Belgium.

C Corresponding author. Email: isabelle.donnay@uclouvain.be

Reproduction, Fertility and Development 21(4) 587-598 https://doi.org/10.1071/RD08147
Submitted: 27 June 2008  Accepted: 6 February 2009   Published: 17 April 2009

Abstract

The aim of the present study was to improve the sanitary quality of in vitro-produced bovine embryos by using plant protein hydrolysates (plant peptones) as substitutes for animal proteins. Peptones were compared with bovine serum albumin (BSA) as the protein source in synthetic oviduct fluid medium and the quality of the resulting embryos was determined. Two batches of peptones (wheat and cotton) were selected on the basis of their anti-oxidant properties. When added to the culture medium, both peptones (at 0.56 mg mL–1 for cotton peptone and at 0.18 mg mL–1 for wheat peptone) led to similar developmental and hatching rates compared with 4 mg mL–1 BSA and embryos were equally resistant to freezing and able to elongate after transfer. Surprisingly, a significant decrease in reduced glutathione (GSH) content was observed when embryos were produced with plant peptone instead of BSA. Supplementation of the culture medium with precursors of GSH (cysteine and β-mercaptoethanol) significantly increased the GSH content. A shift of the sex ratio towards male embryos was seen for Day 8 embryos cultured with wheat peptone, whereas no shift was observed for embryos cultured in the presence of BSA or polyvinylpyrrolidone. In conclusion, culture with plant peptones enables embryos to be obtained at a similar rate and of similar quality to that seen following the use of BSA. The use of the plant peptones increased the sanitary quality of the embryos and decreased the cost of embryo production.


Acknowledgements

The authors thank Rudy De Roover for embryo transfer and recovery and Philippe Bombaerts, Eric Mignolet and Lionel Counet for their technical help. This research was funded by the Ministry of Agriculture of the Région wallonne de Belgique and by the Communauté française de Belgique–Action de Recherches concertées (grant no. 02/07–275).


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