Add like
Add dislike
Add to saved papers

Bioconversion of 5-deoxystrigol stereoisomers to monohydroxylated strigolactones by plants.

The bioconversion of 5-deoxystrigol (5DS) and 4-deoxyorobanchol (4DO), the simplest canonical strigolactones (SLs), into monohydroxylated SLs such as strigol, sorgomol and orobanchol was confirmed by administering of stable isotope-labeled substrates to hydroponically grown plants. Liquid chromatography-mass spectrometry analyses established that 5DS was stereoselectively converted into strigol and sorgomol by cotton ( Gossypium hirsutum ) and Chinese milk vetch ( Astragalus sinicus ), respectively. 4DO was converted into orobanchol by rice ( Oryza sativa ). However, the red bell pepper ( Capsicum annuum ), red clover ( Trifolium pratense ), and pea ( Pisum sativum ) negligibly converted 4DO into orobanchol. The red bell pepper converted ent -4DO into 2',8-bis epi -sorgomol. These results suggest that some plants generate orobanchol without passing through 4DO.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app