Jump to content
 







Main menu
   


Navigation  



Main page
Contents
Current events
Random article
About Wikipedia
Contact us
Donate
 




Contribute  



Help
Learn to edit
Community portal
Recent changes
Upload file
 








Search  

































Create account

Log in
 









Create account
 Log in
 




Pages for logged out editors learn more  



Contributions
Talk
 



















Contents

   



(Top)
 


1 Comparison with mixed acid fermentation  





2 Industrial applications  





3 Alternative bacteria strains  





4 References  





5 Further reading  





6 External links  














Butanediol fermentation






العربية
Deutsch
 

Edit links
 









Article
Talk
 

















Read
Edit
View history
 








Tools
   


Actions  



Read
Edit
View history
 




General  



What links here
Related changes
Upload file
Special pages
Permanent link
Page information
Cite this page
Get shortened URL
Download QR code
Wikidata item
 




Print/export  



Download as PDF
Printable version
 
















Appearance
   

 






From Wikipedia, the free encyclopedia
 


Figure 1: Chemical Structure of 2,3-Butanediol Fermentation

2,3-Butanediol fermentationisanaerobic fermentationofglucose with 2,3-butanediol as one of the end products. The overall stoichiometry of the reaction is

2pyruvate + NADH -->2CO2 + 2,3-butanediol.

Butanediol fermentation is typical for the facultative anaerobes Klebsiella and Enterobacter[1] and is tested for using the Voges–Proskauer (VP) test. There are other alternative strains that can be used, talked about in details in the Alternative Bacteria Strains section below.

Figure 2: The fermentation process to produce butanediol

The metabolic function of 2,3-butanediol is not known, although some have speculated that it was an evolutionary advantage for these microorganisms to produce a neutral product that's less inhibitory than other partial oxidation products and doesn't reduce the pH as much as mixed acids.

There are many important industrial applications that butanediol can be used for, including antifreeze, food additives, antiseptic, and pharmaceuticals. It also is produced naturally in various places of the environment.

Comparison with mixed acid fermentation

[edit]

2,3-butanediol fermentation produces smaller amounts of acid than mixed acid fermentation, and butanediol, ethanol, CO2 and H2 are the end products. While equal amounts of CO2 and H2 are created during mixed acid fermentation, butanediol fermentation produces more than twice the amount of CO2 because the gases are not produced only by formate hydrogen lyase as they are in mixed acid fermentation.

2,3 Butanediol is produced at varying levels in aerated fermentations as long as the dissolved oxygen level is limiting (i.e., the culture is trying to consume more oxygen than is available). The degree of oxygen limitation dictates the ratios of 2,3-butanediol to by-products produced.[2]

Industrial applications

[edit]

2,3-butanediol has a variety of industrial applications and products it can produce. The levo isomer of butanediol has a low freezing point of -60 °C, which allows it to work as an antifreeze agent. Through catalytic dehydrogenation, butanediol can form diacetyl. Diacetyl is a food additive that can be used to add flavor. 0.1% butanediol will kill most pathogenic bacteria due to its antiseptic properties. Through esterification, forms of precursors of polyurethane foams are produced. These can be used in various applications, including in pharmaceuticals, cosmetics, lotions, ointments, and antiperspirants. Butanediol itself even has applications in the pharmaceutical industry as a drug carrier.[3]

Alternative bacteria strains

[edit]

Using mesophilic bacteria requires the fermentation process to occur below 40 °C, which can cause bacterial contamination due to the low temperature. On the industrial scale, this requires sterilization steps which means a special facility must be built, more employees are needed to run this extra step, and more energy is consumed at the plant. A novel aerobic Geobacillus strain XT15 has been shown to produce 2,3-butanediol at a temperature between 45 and 55 °C. This higher temperature will avoid the risk of contamination because microorganisms that live in normal environments cannot reproduce above 45 °C. The Geobacillus strain XT15 is thermophilic, which allows it to be able to operate fermentation at this higher temperature. Sterilization would not be necessary using this alternative strain making the manufacturing process more efficient and cost-effective.[4]

References

[edit]
  1. ^ Geckil H, Barak Z, Chipman DM, Erenler SO, Webster DA, Stark BC (October 2004). "Enhanced production of acetoin and butanediol in recombinant Enterobacter aerogenes carrying Vitreoscilla hemoglobin gene". Bioprocess and Biosystems Engineering. 26 (5): 325–30. doi:10.1007/s00449-004-0373-1. PMID 15309606. S2CID 10019642.
  • ^ Jansen NB, Flickinger MC, Tsao GT (April 1984). "Production of 2,3-butanediol from D-xylose by Klebsiella oxytoca ATCC 8724". Biotechnology and Bioengineering. 26 (4): 362–9. doi:10.1002/bit.260260411. PMID 18553303. S2CID 36290949.
  • ^ Garg SK, Jain A (January 1995). "Fermentative production of 2,3-butanediol: A review". Bioresource Technology. 51 (2–3): 103–109. doi:10.1016/0960-8524(94)00136-o.
  • ^ Xiao Z, Wang X, Huang Y, Huo F, Zhu X, Xi L, Lu JR (December 2012). "Thermophilic fermentation of acetoin and 2,3-butanediol by a novel Geobacillus strain". Biotechnology for Biofuels. 5 (1): 88. doi:10.1186/1754-6834-5-88. PMC 3538569. PMID 23217110.
  • Further reading

    [edit]
    • Madigan M, Martinko J (2006). Brock's Biology of Microorganisms (11th ed.). NJ: Pearson Prentice Hall. pp. 351–355.
    [edit]
    Retrieved from "https://en.wikipedia.org/w/index.php?title=Butanediol_fermentation&oldid=1219068757"

    Category: 
    Fermentation
    Hidden categories: 
    Articles with short description
    Short description matches Wikidata
     



    This page was last edited on 15 April 2024, at 15:19 (UTC).

    Text is available under the Creative Commons Attribution-ShareAlike License 4.0; additional terms may apply. By using this site, you agree to the Terms of Use and Privacy Policy. Wikipedia® is a registered trademark of the Wikimedia Foundation, Inc., a non-profit organization.



    Privacy policy

    About Wikipedia

    Disclaimers

    Contact Wikipedia

    Code of Conduct

    Developers

    Statistics

    Cookie statement

    Mobile view



    Wikimedia Foundation
    Powered by MediaWiki