Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes

Photosynthesis is a key process for converting light energy into chemical energy and providing food for lives on Earth. Understanding the mechanism for the energy transfers could provide insights into regulating energy transfers in photosynthesis and designing artificial photosynthesis systems. Many...

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Main Authors: Ruichao Mao, Xiaocong Wang, Jun Gao
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-10-01
Series:Frontiers in Chemistry
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fchem.2021.764107/full
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spelling doaj-4a7d66bc0f1e42a5a03fc32484b7fec32021-10-04T07:19:39ZengFrontiers Media S.A.Frontiers in Chemistry2296-26462021-10-01910.3389/fchem.2021.764107764107Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational ChangesRuichao MaoXiaocong WangJun GaoPhotosynthesis is a key process for converting light energy into chemical energy and providing food for lives on Earth. Understanding the mechanism for the energy transfers could provide insights into regulating energy transfers in photosynthesis and designing artificial photosynthesis systems. Many efforts have been devoted to exploring the mechanism of temperature variations affecting the excitonic properties of LH2. In this study, we performed all-atom molecular dynamics (MD) simulations and quantum mechanics calculations for LH2 complex from purple bacteria along with its membrane environment under three typical temperatures: 270, 300, and 330 K. The structural analysis from validated MD simulations showed that the higher temperature impaired interactions at N-terminus of both α and β polypeptide helices and led to the dissociation of this hetero polypeptide dimer. Rhodopin-β-D-glucosides (RG1) moved centripetally with α polypeptide helices when temperature increased and enlarged their distances with bacteriochlorophylls molecules that have the absorption peak at 850 nm (B850), which resulted in reducing the coupling strengths between RG1 and B850 molecules. The present study reported a cascading mechanism for temperature regulating the energy transfers in LH2 of purple bacteria.https://www.frontiersin.org/articles/10.3389/fchem.2021.764107/fullphotosynthesislight-harvesting complex 2molecular dynamics simulationenergy transfertemperature effect
collection DOAJ
language English
format Article
sources DOAJ
author Ruichao Mao
Xiaocong Wang
Jun Gao
spellingShingle Ruichao Mao
Xiaocong Wang
Jun Gao
Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
Frontiers in Chemistry
photosynthesis
light-harvesting complex 2
molecular dynamics simulation
energy transfer
temperature effect
author_facet Ruichao Mao
Xiaocong Wang
Jun Gao
author_sort Ruichao Mao
title Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
title_short Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
title_full Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
title_fullStr Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
title_full_unstemmed Bridging Carotenoid-to-Bacteriochlorophyll Energy Transfer of Purple Bacteria LH2 With Temperature Variations: Insights From Conformational Changes
title_sort bridging carotenoid-to-bacteriochlorophyll energy transfer of purple bacteria lh2 with temperature variations: insights from conformational changes
publisher Frontiers Media S.A.
series Frontiers in Chemistry
issn 2296-2646
publishDate 2021-10-01
description Photosynthesis is a key process for converting light energy into chemical energy and providing food for lives on Earth. Understanding the mechanism for the energy transfers could provide insights into regulating energy transfers in photosynthesis and designing artificial photosynthesis systems. Many efforts have been devoted to exploring the mechanism of temperature variations affecting the excitonic properties of LH2. In this study, we performed all-atom molecular dynamics (MD) simulations and quantum mechanics calculations for LH2 complex from purple bacteria along with its membrane environment under three typical temperatures: 270, 300, and 330 K. The structural analysis from validated MD simulations showed that the higher temperature impaired interactions at N-terminus of both α and β polypeptide helices and led to the dissociation of this hetero polypeptide dimer. Rhodopin-β-D-glucosides (RG1) moved centripetally with α polypeptide helices when temperature increased and enlarged their distances with bacteriochlorophylls molecules that have the absorption peak at 850 nm (B850), which resulted in reducing the coupling strengths between RG1 and B850 molecules. The present study reported a cascading mechanism for temperature regulating the energy transfers in LH2 of purple bacteria.
topic photosynthesis
light-harvesting complex 2
molecular dynamics simulation
energy transfer
temperature effect
url https://www.frontiersin.org/articles/10.3389/fchem.2021.764107/full
work_keys_str_mv AT ruichaomao bridgingcarotenoidtobacteriochlorophyllenergytransferofpurplebacterialh2withtemperaturevariationsinsightsfromconformationalchanges
AT xiaocongwang bridgingcarotenoidtobacteriochlorophyllenergytransferofpurplebacterialh2withtemperaturevariationsinsightsfromconformationalchanges
AT jungao bridgingcarotenoidtobacteriochlorophyllenergytransferofpurplebacterialh2withtemperaturevariationsinsightsfromconformationalchanges
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