High-purity steviol glycosides

A stevioside, highly advanced technology, applied in the field of compositions containing stevioside, can solve problems such as inapplicability

Pending Publication Date: 2021-03-16
PURECIRCLE USA
View PDF1 Cites 0 Cited by
  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0005] Although methods for preparing steviol glycosides from Stevia rebaudiana are known, many of these methods are not commercially available

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
  • High-purity steviol glycosides
  • High-purity steviol glycosides
  • High-purity steviol glycosides

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0271] Protein sequences of engineered enzymes used in biocatalytic methods

[0272] SEQ ID 1:

[0273] >SuSy_At, variant PM1-54-2-E05 (engineered sucrose synthase; WT gene source: Arabidopsis)

[0274] MANAERMITRVHSQRERLNETLVSERNEVLALLSRVEAKGKGILQQNQIIAEFEALPEQTRKKLEGGPFFDLLKSTQEAIVLPPWVALAVRPRPGVWEYLRVNLHALVVEELQPAEFLHFKEELVDGVKNGNFTLELDFEPFNASIPRPTLHKYIGNGVDFLNRHLSAKLFHDKESLLPLLDFLRLHSHQGKNLMLSEKIQNLNTLQHTLRKAEEYLAELKSETLYEEFEAKFEEIGLERGWGDNAERVLDMIRLLLDLLEAPDPSTLETFLGRVPMVFNVVILSPHGYFAQDNVLGYPDTGGQVVYILDQVRALEIEMLQRIKQQGLNIKPRILILTRLLPDAVGTTCGERLERVYDSEYCDILRVPFRTEKGIVRKWISRFEVWPYLETYTEDAAVELSKELNGKPDLIIGNYSDGNLVASLLAHKLGVTQCTIAHALEKTKYPDSDIYWKKLDDKYHFSCQFTADIFAMNHTDFIITSTFQEIAGSKETVGQYESHTAFTLPGLYRVVHGIDVFDPKFNIVSPGADMSIYFPYTEEKRRLTKFHSEIEELLYSDVENDEHLCVLKDKKKPILFTMARLDRVKNLSGLVEWYGKNTRLRELVNLVVVGGDRRKESKDNEEKAEMKKMYDLIEEYKLNGQFRWISSQMDRVRNGELYRYICDTKGAFVQPALYEAFGLTVVEAMTCGLPTFATCKGGPAEIIVHGKSGFHIDPYHGDQAADLLADFFTKCKEDPSHWDEISKGGLQRIEEKYTWQIYSQRLLTLTGVYGFWKHVSNLDRLEHRRYLEM...

Embodiment 2

[0282] Expression and formulation of the SuSy_At variant of SEQ ID 1

[0283] The gene encoding the SuSy_At variant of SEQ ID 1 (Example 1) was cloned into the expression vector pLE1A17 (derivative of pRSF-1b, Novagen). The resulting plasmid was used to transform E. coli BL21(DE3) cells.

[0284] Cells were cultured at 37°C in ZYM505 medium (F. Willi AM Studier, Protein Expression and Purification 41 (2005) 207-234) supplemented with kanamycin (50 mg / l). IPTG (0.2 mM) induced gene expression in log phase and at 30°C and 200 rpm for 16-18 hours.

[0285] Cells were harvested by centrifugation (3220xg, 20min, 4°C) and washed with cell lysis buffer (100mM Tris-HClpH7.0; 2mM MgCl 2 , DNA nuclease 20U / mL, lysozyme 0.5mg / mL) resuspended to an optical density of 200 (at 600nm (OD 600 ) measured at ). Cells were then disrupted by sonication and the crude extract was separated from cell debris by centrifugation (18000 xg for 40 min, 4°C). The supernatant was sterilized by filtrati...

Embodiment 3

[0288] Expression and formulation of the UGTS12 variant of SEQ ID 2

[0289] The gene encoding the UGTS12 variant of SEQ ID 2 (Example 1) was cloned into the expression vector pLE1A17 (derivative of pRSF-1b, Novagen). The resulting plasmid was used to transform E. coli BL21(DE3) cells.

[0290] Cells were cultured at 37°C in ZYM505 medium (F. Willi AM Studier, Protein Expression and Purification 41 (2005) 207-234) supplemented with kanamycin (50 mg / l). Gene expression was induced in log phase with IPTG (0.1 mM) at 30°C and 200 rpm for 16-18 hours.

[0291] Cells were harvested by centrifugation (3220xg, 20min, 4°C) and washed with cell lysis buffer (100mM Tris-HCl pH 7.0; 2mM MgCl 2 , DNA nuclease 20U / mL, lysozyme 0.5mg / mL) resuspended to an optical density of 200 (measured at 600nm (OD 600 )). Cells were then disrupted by sonication and the crude extract was separated from cell debris by centrifugation (18000 xg for 40 min, 4°C). The supernatant was sterilized by filtrat...

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

No PUM Login to view more

Abstract

Methods of preparing highly purified steviol glycosides, particularly steviolmonoside, steviolmonoside A, steviolbioside, steviolbioside A, steviolbioside B, rubusoside, stevioside, stevioside A (rebaudioside KA), stevioside B, stevioside C, rebaudioside E, rebaudioside E2, rebaudioside E3, and rebaudioside AM are described. The methods include utilizing enzyme preparations and recombinant microorganisms for converting various staring compositions to target steviol glycosides. The highly purified rebaudiosides are useful as non-caloric sweetener, flavor enhancer, sweetness enhancer, and foaming suppressor in edible and chewable compositions such as any beverages, confectioneries, bakery products, cookies, and chewing gums.

Description

technical field [0001] The present invention relates to compositions comprising steviol glycosides, including highly purified steviol glycoside compositions, and methods for preparing them. [0002] Background of the invention [0003] High intensity sweeteners have a sweetness level that is many times greater than the sweetness level of sucrose. They are primarily non-caloric and are often used in meals and reduced-calorie products, including food and beverages. High-intensity sweeteners do not elicit an insulin-elevating response, making them suitable for products targeting diabetes and others beneficial in controlling their sugar intake. [0004] Steviol glycosides are a class of compounds found in the leaves of Stevia rebaudiana Bertoni, a perennial shrub in the family Asteraceae (Compositae) native to certain regions of South America. Their structure is characterized by the monobasic steviol, distinguished by the presence of carbohydrate residues at the C13 and C19 pos...

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): C07H15/256A23L27/30C12N9/10C12P19/56
CPCC07H15/256C12P19/56A23L27/36A23L27/88C12N9/1062C12N9/1051C07H1/00
Inventor A·马科斯雅恩S·A/L·拉曼达赫M·阿弗扎尔宾哈希姆K·尼扎姆宾纳维S·Y·周S·普尔卡亚萨M·派蒂特
Owner PURECIRCLE USA
Who we serve
  • R&D Engineer
  • R&D Manager
  • IP Professional
Why Eureka
  • Industry Leading Data Capabilities
  • Powerful AI technology
  • Patent DNA Extraction
Social media
Try Eureka
PatSnap group products

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

© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap