1 / 16

Novel Aminomethanesulfonate Buffers for Biological Buffering in the Acidic Range *

Novel Aminomethanesulfonate Buffers for Biological Buffering in the Acidic Range *. Robert D. Long, Newton P. Hilliard Jr., Daniel Dei, Enoch A. Mensah. Paper # 432. * Patent pending. Goal. New buffers for biological systems at pH levels well into acidic range (below pH 5.5)

nedra
Download Presentation

Novel Aminomethanesulfonate Buffers for Biological Buffering in the Acidic Range *

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript


  1. Novel Aminomethanesulfonate Buffers for Biological Buffering in the Acidic Range* Robert D. Long, Newton P. Hilliard Jr., Daniel Dei, Enoch A. Mensah Paper # 432 * Patent pending

  2. Goal New buffers for biological systems at pH levels well into acidic range (below pH 5.5) • Needed for acidophilic bacteria studies • Enzyme/biotech systems at acidic pH • “Good” buffers limited usability below physiological range • Metabolic interferences from citrate, borate, phosphate, and other systems

  3. “Good” Buffers • Tertiary or secondary amines with alkylsulfonic acid attached (varying alkyl chain length) Ref: Good, N. E., et al. Biochemistry1966, 5(2), 467-477. Good, N. E., and Izawa, S. Methods Enzymol.1980, 24, 53-68.

  4. Desirable Properties (per N. Good) • midrange pKa • maximum water solubility and minimum solubility in all other solvents • minimal salt effects • minimal change in pKa with temperature • chemically and enzymatically stable • minimal absorption in visible or UV spectral range and • reasonably easily synthesized.

  5. Some Lower pH Good Buffers

  6. Target Compounds

  7. Routes to Current Good Buffers

  8. Synthesis of Aminomethanesulfonates Ref: Johnson, T.B. JACS 1941, 63, 1571-1572. Raschig, F.; Prahl, W., Ann.1926, 448, 265. Gilbert, E. E., Sulfonation and Related Reactions; Interscience; NY, 1965 Ref: Knoevenagel, E., Ber. 1904, 37, 4087. Neelakantan & Hartung, JOC1959, 24, 1943.

  9. Synthesis of Other Targets

  10. Ionization of Aminoalkylsulfonates MMS – morpholinomethanesulfonic acid

  11. Crystallography of MMS Sodium salt form (no protonation)

  12. Crystallography of HEPMS Note: Zwitterion Protonated amine Sulfonate anion

  13. pKa Comparison * pKa2 value

  14. Initial Growth Studies E. coli strain HB101 at pH 7.2 and 37ºC for 18 hours

  15. In-progress Biological Testing • Halothiobacillus neapolitanus at acidic pH • E. coli & H. neapolitanus transformation efficiency • Enzyme reactions (food technology/ glycosidases) in the acidic range Preliminary testing shows increased efficiency/activity in all three areas with MMS

  16. Acknowledgements • BRIN/INBRe (NIH-NCRR P20-016840) (Infrastructure grant) • Dr. Newton Hilliard (Biochemistry) • Grad students • Enoch Mensah • Daniel Dei • Science & Technology Corp. (STC) at Univ. of New Mexico (Patent pending) (For more info contact robert.long@enmu.edu or ssheehan@unm.edu)

More Related