Advertisement

Organic acid seperation from bacterial cultures need help

Discussions about HPLC, CE, TLC, SFC, and other "liquid phase" separation techniques.

4 posts Page 1 of 1
Hi.
I am struggling with some Glucose in my Organic acid experiment.
I am using Synergi Hydro RP column for seperating organic acids from bacterial cultures.
(Flow rate 0.7 ml/min, 20mM KH2PO4 pH 2.9 detection at 220 nm, isoratic)

I was able to obtain very clean peak for all my standards ( Oxalic acid, D-gluconic acid, Citric, Acetic, Lactic, Malic, etc..)
But whenever I examine my bacterial culture samples D-gluconic acid peak rises too high.
I think it has something to do with D-glucose in the media. (retention time of D-glucose was exactly same as D-gluconic acid.. as expected....)

So, here is my question..
Because I can't use sucrose or lactose for my bacterial culture media, I need to use D-glucose for my experiment.
Is there any ways to distinguish D-glucose from D-gluconic acid by HPLC? something like, extra sample preparation steps perhaps? or do I need to try out a new column?


Any suggestions will be greatful.
Thanks in advance

Yours
Young
Hellow
1) Big peak.
D-gluconic acid has a "conjugate relationship" from carboxylic to aldol groups , pair of electrons multiplies the absorption of light at 220 nm. Its normal . Solve problem - dissolve (dilute) the sample.
2) Glucose and gluconic acids not selected on hydro-RP.
This substances were polar and good dissolve in water . Glucose slighty sorbed in hydrophobes (RP-C8 RP--C18) and semi-hydrophilic (Hydro-RP) sorbents and jump out in a first minutes.
Ideal - use the aminophase column . Aminophase good sorbed aldehyde (pairing electrone mechanism) and acids (ion pair mechanism).
Variant => use SPE which aminophase .
Anohter (bad) variant- use dinamic modification column (such hexylamine buffer).
The use of an HILIC column maybe also a good alternative.
Gerhard Kratz, Kratz_Gerhard@web.de
You should not have any problem separation these compounds if you are using correct tools. Sugars are neutral and polar, acids are polar and acidic. Just use HILIC/Ion exchange:
http://www.sielc.com/Application-Effect ... Acids.html
http://www.sielc.com/Application-HILIC- ... Acids.html
Vlad Orlovsky
HELIX Chromatography
My opinions might be bias, but I have about 1000 examples to support them. Check our website for new science and applications
www.helixchrom.com
4 posts Page 1 of 1

Who is online

In total there are 20 users online :: 1 registered, 0 hidden and 19 guests (based on users active over the past 5 minutes)
Most users ever online was 4374 on Fri Oct 03, 2025 12:41 am

Users browsing this forum: Amazon [Bot] and 19 guests

Latest Blog Posts from Separation Science

Separation Science offers free learning from the experts covering methods, applications, webinars, eSeminars, videos, tutorials for users of liquid chromatography, gas chromatography, mass spectrometry, sample preparation and related analytical techniques.

Subscribe to our eNewsletter with daily, weekly or monthly updates: Food & Beverage, Environmental, (Bio)Pharmaceutical, Bioclinical, Liquid Chromatography, Gas Chromatography and Mass Spectrometry.

Liquid Chromatography

Gas Chromatography

Mass Spectrometry