Looking for breakthrough ideas for innovation challenges? Try Patsnap Eureka!

Peptides containing tryptophan

a technology of tryptophan and peptides, which is applied in the direction of peptide/protein ingredients, drug compositions, biocides, etc., can solve the problems of difficult complete separation of alpha-lactalbumin, inability to fully separate alpha-lactalbumin, and inability to achieve the maximum trp/lnaa ratio and cost, etc., to improve alertness, mood, cognition or sleep patterns, and relieve stress or depression.

Inactive Publication Date: 2011-04-14
DSM IP ASSETS BV
View PDF4 Cites 22 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0009]This composition is preferably a lysozyme hydrolysate or a purified lysozyme hydrolysate. In one embodiment of the invention, the lysozyme hydrolysate is particularly rich in arginine residues. Arginine does not belong to the group large, neutral amino acids (LNAA's) but is known for its insulin stimulating effect. We have found that the hydrolysate according to the invention can generate in vivo high blood plasma Trp / LNAA ratios. Quite surprisingly the Trp / LNAA ratios detected in blood plasma, were found to be higher than the Trp / LNAA ratio of the hydrolysate. Yet another advantage of the invention is that the Trp containing peptides are very small so that even in combination with protein-rich products with less favorable Trp / LNAA ratios, the hydrolysate can immediately generate high blood plasma Trp / LNAA ratios. The composition may further comprise free tryptophan. Preferably the hydrolysate does not contain more than 1 wt % (on dry matter) of free tryptophan.

Problems solved by technology

However, in many countries legislation exists that tightly regulates the supply of free tryptophan.
However, the use of alpha-lactalbumin as a starting point for tryptophan-rich preparations, comes with disadvantages in terms of maximal Trp / LNAA ratios and costs.
Because on an industrial scale a complete separation of alpha-lactalbumin and beta-lactoglobulin is difficult, the, implication is that cost effective alpha-lactalbumin preparations will contain beta-lactoglobulin as well.
So obviously any contamination of the alpha-lactalbumin preparation with beta-lactoglobulin, will dramatically lower the Trp / LNAA ratio of the final product.

Method used

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
View more

Image

Smart Image Click on the blue labels to locate them in the text.
Viewing Examples
Smart Image
  • Peptides containing tryptophan
  • Peptides containing tryptophan
  • Peptides containing tryptophan

Examples

Experimental program
Comparison scheme
Effect test

example 1

Hen Egg Lysozyme is not Cleaved by Either Pepsin or Trypsin / Chymotrypsin

[0078]To test its digestibility in the human gastrointestinal tract, hen egg lysozyme was incubated in vitro with pepsin as well as with a mixture of trypsin and chymotrypsin. Both incubations were carried out under pH conditions that are prevalent in the stomach (pepsin) and duodenum (trypsin / chymotrypsin). To that end, a 5% (w / w) lysozyme solution was incubated with the enzymes (1% w / w enzyme to lysozyme protein) for 2 hours at 37 degrees C. To prevent major pH changes as the result of the ongoing protein hydrolysis, incubation was carried out in a Mc Ilvane buffer (0.2 M citric acid plus Na2HPO4). The low DH's values that are obtained after the two hours hydrolysis at 37 degrees C. (see Table 1), demonstrate that the lysozyme molecule cannot be degraded under conditions that mimic digestion conditions in the stomach and in the duodenum and jejunum because successful proteolysis can be expected to lead to a DH...

example 2

Hen Egg Lysozyme is Efficiently Cleaved by Subtilisin at Elevated pH Values

[0079]To test the susceptibility of lysozyme to enzyme hydrolysis under non-physiological pH and enzyme conditions, a lysozyme solution was incubated in vitro with a microbial subtilisin (EC 3.4.21.62) under alkaline pH conditions. To that end, a 5% (w / w) lysozyme solution was incubated at pH 7.0, 8.0 and 9.0 with 12.5 microliter of Protex 6L.per gram lysozyme protein present. The incubation was carried out for 3 hours at 60 degrees C. with a constant adjustment of the pH using 1M NaOH. The incubations yielded slightly turbid solutions without any significant precipitates. After a heating step to inactivate the subtilisin activity, the DH values of the various incubations were measured according to the protocol described in the Materials& Methods section. In contrast with the results obtained under physiological conditions (see Example 1), alkaline incubation conditions using subtilisin result in complete lys...

example 3

Hydrolysing Lysozyme Using Protex and Identity of the Peptides Formed

[0080]A solution containing 10% (w / w) pure lysozyme was adjusted to pH 8.2 using NaOH and heated to 52 degrees C. Hydrolysis was started by adding 25 microliter of

[0081]Protex / g of protein present. Under continuous stirring and maintaining the pH at 8.2, the hydrolysis was continued for 5.5 hours to yield an almost clear solution without a visible precipitate. After a heating step to inactivate the Protex activity, a sample was taken for DH analysis. The DH of the solution turned out to be almost 30%. The heat treated solution was ultrafiltered over a 10 kDa filter to yield a completely clear liquid. This clear liquid was used for LC / MS analysis, for molecular weight distribution of peptides and proteins present as well as for ion exchange chromatography.

[0082]To get an impression of the molecular weight distribution of peptides and proteins present, the clear liquid was subjected to a molecular size analysis as de...

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

PUM

PropertyMeasurementUnit
Volumeaaaaaaaaaa
Fractionaaaaaaaaaa
Fractionaaaaaaaaaa
Login to View More

Abstract

The present invention relates to a process to produce a composition comprising water-soluble peptides and having a Trp / LNAA ratio of more than 0.15, which comprises hydrolyzing lysozyme, preferably hen eggs lysozyme, to prepare a hydrolysate having a DH of between 5 and 45.

Description

FIELD OF THE INVENTION[0001]The present invention relates to peptides comprising tryptophan residues.BACKGROUND OF THE INVENTION[0002]Serotonine levels in the brain have been linked with mood, alertness, vigilance, sleep onset and quality, anxiolytic effects, depression, affective reaction control, appetite and sexual behavior. Many publications exist in which changes in brain serotonin levels are correlated with the availability of the natural amino acid L-tryptophan (Trp or W).[0003]Because of this correlation, methods to increase plasma tryptophan levels have received a lot of attention. Tryptophan quantities of around 1 gram / day per individual have been reported to yield clinically significant effects (Markus et al., Am. J Clin. Nutr 2005;81, 1026-1033). One method to increase plasma tryptophan levels involves the consumption of protein preparations enriched in the whey protein alpha-lactalbumin. Alpha-lactalbumin preparations are readily available and have a relatively high try...

Claims

the structure of the environmentally friendly knitted fabric provided by the present invention; figure 2 Flow chart of the yarn wrapping machine for environmentally friendly knitted fabrics and storage devices; image 3 Is the parameter map of the yarn covering machine
Login to View More

Application Information

Patent Timeline
no application Login to View More
IPC IPC(8): A61K38/17C12P21/06
CPCC12P13/22C12P21/06A61K38/06A23L1/3053A61K38/05A23K1/1631A23K20/147A23L33/18A61P1/14A61P25/00
Inventor DE ROOS, ANDRE LEONARDUSEDENS, LUPPOVAN BECKHOVEN, RUDOLF FRANCISCUSDUCHATEAU, ALEXANDER LUCIA LEONARDUSKLOEK, JORIS
Owner DSM IP ASSETS BV
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Patsnap Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Patsnap Eureka Blog
Learn More
PatSnap group products

Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com