Use of proline tolerant tripeptidyl peptidases in feed additive compositions

Patent metadata

Field	Value
Publication number	US-2020245642-A1
Application number	US-202016744752-A
Country	US
Kind code	A1
Filing date	Jan 16, 2020
Priority date	Oct 24, 2014
Publication date	Aug 6, 2020
Grant date	—

Abstract

A method of preparing a feed additive composition comprising: (a) admixing at least one proline tolerant tripeptidyl peptidase predominantly having exopeptidase activity wherein said proline tolerant tripeptidyl peptidase is capable of cleaving tri-peptides from the N-terminus of peptides having (i) (A) Proline at P1; and (B) An amino acid selected from alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tryptophan, tyrosine, valine or synthetic amino acids at P1; or (ii) (a′) Proline at PV; and (b′) An amino acid selected from alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tryptophan, tyrosine, valine or synthetic amino acids or amines at PV; and one or more ingredients selected from the group consisting of a salt, polyol including sorbitol and glycerol, wheat or a wheat component, sodium acetate, sodium acetate trihydrate, potassium sorbate Talc, polyvinyl alcohol (PVA), benzoate, sorbiate, 1,3-propane diol, glucose, parabens, sodium chloride, citrate, metabisulfite, formate or a combination thereof; and (b) optionally packaging as well as uses of such proline tolerant tripeptidyl peptidases, feed additive compositions, feed additive kits, feeds or feedstuffs and/or premixes.

First claim

1 - 37 . (canceled)

38 . A non-therapeutic method for improving a biophysical characteristic of an animal or for improving protein digestibility of an animal which method comprises administering to an animal at least one proline tolerant tripeptidyl peptidase predominantly having exopeptidase activity wherein said proline tolerant tripeptidyl peptidase is capable of cleaving tri-peptides from the N-terminus of peptides having:
(i)
(A) proline at P1; and
(B) an amino acid selected from alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tryptophan, tyrosine, valine or synthetic amino acids at P1; and/or
(ii)
(a′) proline at P1; and
(b′) an amino acid selected from alanine, arginine, asparagine, aspartic acid, cysteine, glutamine, glutamic acid, glycine, histidine, isoleucine, leucine, lysine, methionine, phenylalanine, serine, threonine, tryptophan, tyrosine, valine or synthetic amino acids or amines at P1′; and

optionally at least one feed component and/or at least one mineral and/or at least one vitamin, preferably wherein the method comprises administering to an animal at least one endoprotease, wherein the at least one proline tolerant tripeptidyl peptidase:
(a) comprises the amino acid sequence SEQ ID No. 29, SEQ ID No. 1, SEQ ID No. 2 or a functional fragment thereof that retains said peptidase activity;
(b) comprises an amino acid having at least 80% or at least 90% identity to SEQ ID No. 29, SEQ ID No. 1, SEQ ID No. 2 or a functional fragment thereof that retains said peptidase activity;
(c) is encoded by a nucleotide sequence comprising the sequence SEQ ID No. 56;
(d) is encoded by a nucleotide sequence comprising at least 80% or at least 90% sequence identity to SEQ ID No. 56;
(e) is encoded by a nucleotide sequence which hybridises to SEQ ID No. 56 under high stringency conditions; or
(f) is encoded by a nucleotide sequence which differs from SEQ ID No. 56 due to degeneracy of the genetic code.

39 . The method according to claim 38 , wherein the biophysical characteristic is selected from the group consisting of one or more of the following: performance of the animal, growth performance of an animal, feed conversion ratio (FCR), ability to digest a raw material (e.g. nutrient digestibility, including starch, fat, protein, fibre digestibility), nitrogen digestibility (e.g. ileal nitrogen digestibility) and digestible energy (e.g. ileal digestible energy), nitrogen retention, carcass yield, growth rate, weight gain, body weight, mass, feed efficiency, body fat percentage, body fat distribution, growth, egg size, egg weight, egg mass, egg laying rate, lean gain, bone ash %, bone ash mg, back fat %, milk output, milk fat %, reproductive outputs such as litter size, litter survivability, hatchability % and environmental impact, e.g. manure output and/or nitrogen excretion, preferably wherein the biophysical characteristic is the ability to digest protein.

40 . A method according to claim 38 :
(a) wherein the at least one endoprotease, proline tolerant tripeptidyl peptidase or combination thereof is admixed with the at least one protein or portion thereof immediately prior to feeding the feed additive composition to an animal; and/or (b) wherein the at least one endoprotease, proline tolerant tripeptidyl peptidase or combination thereof is activated by feeding the at least one endoprotease, tripeptidyl peptidase or combination thereof to an animal; and/or (c) the endoprotease and proline tolerant tripeptidyl peptidase is functional, or primarily functional, in the gastrointestinal tract of the animal; and/or (d) the at least one endoprotease and at least one proline tolerant tripeptidyl peptidase are active in the duodenum and parts of the gastrointestinal tract of the animal preceding the duodenum; and/or (e) when fed to an animal the feed additive composition does not substantially increase the incidence of necrotic enteritis in said animal when compared to an animal not fed said feed additive composition.

Assignees

• Dupont Nutrition Biosci Aps

Inventors

• Haaning Svend
• Kragh Karsten Matthias
• Shipovskov Stepan
• Miasnikov Andrei
• Ma Maria
• Millan Luis Fernando Romero
• Barnard Luke
• Yu Shukun
• Meinjohanns Ernst
• Bak Steffen Yde
• NURMINEN Päivi
• Anglenius Heli

Classifications

• C12Y304/14009

  Tripeptidyl-peptidase I (3.4.14.9) · CPC title

• C12Y304/14

  Dipeptidyl-peptidases and tripeptidyl-peptidases (3.4.14) · CPC title

• C12P21/06

  produced by the hydrolysis of a peptide bond, e.g. hydrolysate products (preparing foodstuffs by protein hydrolysis A23J3/00) · CPC title

• C12N9/485

  Exopeptidases (3.4.11-3.4.19) · CPC title

• C12N9/48

  acting on peptide bonds (3.4) · CPC title