Jump to content
Main menu
Main menu
move to sidebar
hide
Navigation
Main page
Recent changes
Random page
Help about MediaWiki
Special pages
Niidae Wiki
Search
Search
Appearance
Create account
Log in
Personal tools
Create account
Log in
Pages for logged out editors
learn more
Contributions
Talk
Editing
Chemistry of ascorbic acid
(section)
Page
Discussion
English
Read
Edit
View history
Tools
Tools
move to sidebar
hide
Actions
Read
Edit
View history
General
What links here
Related changes
Page information
Appearance
move to sidebar
hide
Warning:
You are not logged in. Your IP address will be publicly visible if you make any edits. If you
log in
or
create an account
, your edits will be attributed to your username, along with other benefits.
Anti-spam check. Do
not
fill this in!
===Industrial preparation=== [[Image:Synthesis ascorbic acid.svg|thumb|500px|class=skin-invert-image|The outdated but historically significant industrial synthesis of ascorbic acid from glucose via the [[Reichstein process]]]] Seventy percent of the world's supply of ascorbic acid is produced in China.<ref name="Vantage Market Research-2022" /> Ascorbic acid is prepared in industry from [[glucose]] in a method based on the historical [[Reichstein process]]. In the first of a five-step process, glucose is catalytically [[hydrogenation|hydrogenated]] to [[sorbitol]], which is then [[redox|oxidized]] by the [[microorganism]] ''[[Acetic acid bacteria#Acetobacter|Acetobacter]] suboxydans'' to [[sorbose]]. Only one of the six hydroxy groups is oxidized by this enzymatic reaction. From this point, two routes are available. Treatment of the product with [[acetone]] in the presence of an acid [[Catalysis|catalyst]] converts four of the remaining [[hydroxyl]] groups to [[acetal]]s. The unprotected hydroxyl group is oxidized to the carboxylic acid by reaction with the catalytic oxidant [[TEMPO]] (regenerated by [[sodium hypochlorite]]{{snd}} [[bleach]]ing solution). Historically, industrial preparation via the Reichstein process used [[potassium permanganate]] as the bleaching solution. Acid-catalyzed hydrolysis of this product performs the dual function of removing the two acetal groups and [[lactone|ring-closing lactonization]]. This step yields ascorbic acid. Each of the five steps has a yield larger than 90%.<ref>{{Ullmann | author = Eggersdorfer, M. |display-authors=etal| title = Vitamins | doi = 10.1002/14356007.a27_443 }}</ref> A biotechnological process, first developed in China in the 1960s but further developed in the 1990s, bypasses acetone-protecting groups. A second [[genetically modified]] microbe species, such as mutant ''[[Erwinia]]'', among others, oxidises sorbose into 2-ketogluconic acid (2-KGA), which can then undergo ring-closing lactonization via dehydration. This method is used in the predominant process used by the ascorbic acid industry in China, which supplies 70% of the world's ascorbic acid.<ref name="Vantage Market Research-2022">{{cite press release |url=https://www.globenewswire.com/en/news-release/2022/11/08/2550571/0/en/Global-Vitamin-C-Market-Size-Share-to-Surpass-1-8-Bn-by-2028-China-Produces-80-of-Commercial-Vitamin-C-Vantage-Market-Research.html |title=Vantage Market Research: Global Vitamin C Market Size & Share to Surpass $1.8 Bn by 2028 |date=8 November 2022 |website=Globe Newswire |access-date=21 December 2023}}</ref> Researchers are exploring means for one-step fermentation.<ref>{{cite journal |vauthors=Zhou M, Bi Y, Ding M, Yuan Y |title=One-Step Biosynthesis of Vitamin C in Saccharomyces cerevisiae |journal=Front Microbiol |volume=12 |issue= |pages=643472 |date=2021 |pmid=33717042 |pmc=7947327 |doi=10.3389/fmicb.2021.643472 |url= |doi-access=free }}</ref><ref>{{cite journal |vauthors=Tian YS, Deng YD, Zhang WH, Yu-Wang, Xu J, Gao JJ, Bo-Wang, Fu XY, Han HJ, Li ZJ, Wang LJ, Peng RH, Yao QH |display-authors=5 |title=Metabolic engineering of Escherichia coli for direct production of vitamin C from D-glucose |journal=Biotechnol Biofuels Bioprod |volume=15 |issue=1 |pages=86 |date=August 2022 |pmid=35996146 |pmc=9396866 |doi=10.1186/s13068-022-02184-0 |url= |doi-access=free |bibcode=2022BBB....15...86T }}</ref>
Summary:
Please note that all contributions to Niidae Wiki may be edited, altered, or removed by other contributors. If you do not want your writing to be edited mercilessly, then do not submit it here.
You are also promising us that you wrote this yourself, or copied it from a public domain or similar free resource (see
Encyclopedia:Copyrights
for details).
Do not submit copyrighted work without permission!
Cancel
Editing help
(opens in new window)
Search
Search
Editing
Chemistry of ascorbic acid
(section)
Add topic