Abstract
Carbohydrates, or in strictly chemical terms, polyhydroxy-aldehydes or ketones represent enormous structural diversity in terms of the arrangement of atoms in space, resulting in hundreds of stereoisomers. Although the chemical properties of most stereoisomers may not be very different, their metabolic fate and utilization in biological systems is significantly different and known to influence the overall carbohydrate metabolism. This dictates the importance of understanding the structures of various stereochemical structures for a biochemist. At graduate level teaching, it is really a challenging task to correlate, connect, and recall all the structures. Conventional teaching methods and standard textbook illustrations seldom enable the learners and instructors to sustain the information for a prolonged period. We, in this article, present a unique approach and introduce sigma notation rules for the correlation of stereochemistry of carbohydrates in order to enhance the understanding of stereochemical structures. © 2019 International Union of Biochemistry and Molecular Biology, 48(1):8-20, 2020.
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
More From: Biochemistry and molecular biology education : a bimonthly publication of the International Union of Biochemistry and Molecular Biology
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.