Photolyase Production and Current Applications: A Review
- Diana Ramírez-Gamboa,
- Ana Laura Díaz-Zamorano,
- Edgar Ricardo Meléndez-Sánchez,
- Humberto Reyes-Pardo,
- Karen Rocio Villaseñor-Zepeda,
- Miguel E. López-Arellanes
- Instituto Tecnologico de Estudios Superiores de Monterrey,
- ,
- Harvard University,
- Massachusetts Institute of Technology
Research Output:
Contribution to journal
Review article
Peer-reviewOpen access
Sustainable Development Goals
- SDG 3 Good Health and Well
Publication metrics
Metrics
SciVal
FWCI
0.77
SciVal
Author count
13
SciVal
Paper percentile
63
SciVal
Citations
35
Abstract
The photolyase family consists of flavoproteins with enzyme activity able to repair ultraviolet light radiation damage by photoreactivation. DNA damage by the formation of a cyclobutane pyrimidine dimer (CPD) and a pyrimidine-pyrimidone (6-4) photoproduct can lead to multiple affections such as cellular apoptosis and mutagenesis that can evolve into skin cancer. The development of integrated applications to prevent the negative effects of prolonged sunlight exposure, usually during outdoor activities, is imperative. This study presents the functions, characteristics, and types of photolyases, their therapeutic and cosmetic applications, and additionally explores some photolyase-producing microorganisms and drug delivery systems.
Publication Information
Output type
Research Output:
Contribution to journal
Review article
Peer-reviewOriginal language
EnglishArticle number
5998Journal (Volume, Issue Number)
Molecules (Volume 27, Issue 18)Publication milestones
- Published - 09/2022
Publication status
Published - 09/2022
ISSN
1420-3049Publication IDs
- Scopus: 85138349014
- PubMed: 36144740
Funding Details
This work was also partially supported by Consejo Nacional de Ciencia y Tecnología (CONACYT) under Sistema Nacional de Investigadores (SNI) program awarded to Manuel Martínez Ruiz (CVU: 418151), Juan Eduardo Sosa-Hernández (CVU: 375202), Roberto Parra-Saldívar (CVU: 35753) and Hafiz M.N. Iqbal (CVU: 735340). Figures were created with BioRender.com.
This research was supported by NET ZERO RESEARCH FUND (2021 call) from The Bank of Nova Scotia. The funding number is not applicable.
FundersFunding numbers
Bank of Nova Scotia
-CONACYT
-SNI
35753, 375202, 735340, 418151
