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. 2022 Apr 6;12(7):935.
doi: 10.3390/ani12070935.

Biomarkers and De Novo Protein Design Can Improve Precise Amino Acid Nutrition in Broilers

Affiliations

Biomarkers and De Novo Protein Design Can Improve Precise Amino Acid Nutrition in Broilers

María Cambra-López et al. Animals (Basel). .

Abstract

Precision nutrition in broilers requires tools capable of identifying amino acid imbalances individually or in groups, as well as knowledge on how more digestible proteins can be designed for innovative feeding programs adjusted to animals' dynamic requirements. This work proposes two potential tools, combining traditional nutrition with biotechnological, metabolomic, computational and protein engineering knowledge, which can contribute to improving the precise amino acid nutrition of broilers in the future: (i) the use of serum uric nitrogen content as a rapid biomarker of amino acid imbalances, and (ii) the design and modeling of de novo proteins that are fully digestible and fit exactly to the animal's requirements. Each application is illustrated with a case study. Case study 1 demonstrates that serum uric nitrogen can be a useful rapid indicator of individual or group amino acid deficiencies or imbalances when reducing dietary protein and adjusting the valine and arginine to lysine ratios in broilers. Case study 2 describes a stepwise approach to design an ideal protein, resulting in a potential amino acid sequence and structure prototype that is ideally adjusted to the requirements of the targeted animal, and is theoretically completely digestible. Both tools can open up new opportunities to form an integrated framework for precise amino acid nutrition in broilers, helping us to achieve more efficient, resilient, and sustainable production. This information can help to determine the exact ratio of amino acids that will improve the efficiency of the use of nitrogen by poultry.

Keywords: PLF; ideal protein; poultry; precise feeding; precision livestock farming.

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Relationship between animal’s serum uric nitrogen (SUN), when fed the different experimental diets varying in crude protein, as well as valine and arginine to lysine ratios (T1 to T4), and individual average daily weight gain during the last period of the grower phase (day 28 to 35) in broilers (n = 21 animals per treatment). T1: 20% crude protein content, valine/lysine ratio (0.80) and arginine/lysine ratio (1.05) formulated according to current recommendations; T2: 18% crude protein content and valine/lysine ratio (0.80) and arginine/lysine ratio (1.05) formulated according to current recommendations; T3: 18% crude protein content, below-required valine/lysine ratio (0.70) and arginine/lysine ratio (1.05) formulated according to current recommendations; T4: 18% crude protein content, below-required arginine/lysine ratio (0.92) and valine/lysine ratio (0.80) formulated according to current recommendations.
Figure 2
Figure 2
Original 108-amino acid sequence (Round 3) and refined sequence with 112 amino acids modeled for complete digestion (Round 3.1, Round 3.2, Round 3.3 and Round 3.4). One-letter amino acid code: A—alanine, C—cysteine, D—aspartic acid, E—glutamic acid, F—phenylalanine, G—glycine, H—histidine, I—isoleucine, K—lysine, L—leucine, M—methionine, N—asparagine, P—proline, Q—glutamine, R—arginine, S—serine, T—threonine, V—valine, W—tryptophan, Y—tyrosine.
Figure 3
Figure 3
Predicted secondary and tertiary structure of sequence Round 3.3 by I-TASSER. (a) Three-dimensional tertiary structure cartoon model. In pink α-helices, in yellow β-sheets and in white coil regions. (b) Secondary predicted structure. H: α-helices; S: β-sheets; C: coil regions based on in silico digestion of initial designed sequences for primary structure. One letter amino acid code: A—alanine, C—cysteine, D—aspartic acid, E—glutamic acid, F—phenylalanine, G—glycine, H—histidine, I—isoleucine, K—lysine, L—leucine, M—methionine, N—asparagine, P—proline, Q—glutamine, R—arginine, S—serine, T—threonine, V—valine, W—tryptophan, Y—tyrosine.
Figure 4
Figure 4
Protein 3D structure model of Round 3.1 using (a) the I-TASSER model and (b) the QUARK model.
Figure 5
Figure 5
Integrated framework scheme for precise amino acid nutrition in broiler farming, combining nutritional strategies and feeding technologies.

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