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ARS Home » Plains Area » College Station, Texas » Southern Plains Agricultural Research Center » Insect Control and Cotton Disease Research » Research » Publications at this Location » Publication #288039


Location: Insect Control and Cotton Disease Research

Title: Quantitate gossypol enantiomers in cotton flower petals and seed using capillary electrophoresis

item Vshivkov, Sergei
item Pshenichnov, Egor
item Golubenko, Zamira
item Akhunov, Alik
item Namazov, Shadman
item Bell, Alois - Al
item Stipanovic, Robert - Bob

Submitted to: National Cotton Council Beltwide Cotton Conference
Publication Type: Abstract Only
Publication Acceptance Date: 12/13/2012
Publication Date: 1/16/2013
Citation: Vshivkov, S., Pshenichnov, E., Golubenko, Z., Akhunov, A., Namazov, S., Bell, A.A., Stipanovic, R.D. 2013. Quantitate gossypol enantiomers in cotton flower petals and seed using capillary electrophoresis. National Cotton Council Beltwide Cotton Conference, January 7-10, 2013, San Antonio, Texas. CDROM

Interpretive Summary:

Technical Abstract: Gossypol is a compound that occurs in the cotton plant and in leaves it protects the plant from insect herbivory. The compound also occurs in the seed. In this tissue it renders the seed toxic to non-ruminant animals. However, gossypol exists as a mixture of enantiomers referred to as (+)-gossypol and (-)-gossypol. The (-)-enantiomer is more toxic to non-ruminant animals. We have developed cotton plants with a low level of (-)-gossypol in the seed. The seed from these plants are less toxic to chickens than normal cottonseed. To breed plants with the high (+)-gossypol seed trait, the percentage of (+)- and (-)-gossypol must be determined in the flower petals and seed. This was previously accomplished using high performance liquid chromatography which requires the use of expensive solvents. We now report a method to quantitatively determine the total gossypol and percent of its enantiomers in cotton tissues using high performance capillary electrophoresis (HPCE). The method utilizes a borate buffer at pH 9.3 using a capillary with internal diameter of 50 micron, effective length of 24.5 cm, 15 kV and cassette temperature of 15°C. This method provides high accuracy and reproducible results with a limit of detection of the individual enantiomers of less than 36 ng/mL providing base line separation in less than 6 minutes.