Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions

ABSTRACT Cyanobacteria are promising industrial platforms owing to their ability to produce diverse natural secondary metabolites and nonnative value-added biochemicals from CO2 and light. To fully utilize their industrial potency, it is critical to understand their photosynthetic efficiency under v...

Full description

Bibliographic Details
Main Authors: Sang-Hyeok Cho, Yujin Jeong, Seong-Joo Hong, Hookeun Lee, Hyung-Kyoon Choi, Dong-Myung Kim, Choul-Gyun Lee, Suhyung Cho, Byung-Kwan Cho
Format: Article
Language:English
Published: American Society for Microbiology 2021-12-01
Series:mSystems
Subjects:
Online Access:https://journals.asm.org/doi/10.1128/mSystems.00943-21
_version_ 1818979280234741760
author Sang-Hyeok Cho
Yujin Jeong
Seong-Joo Hong
Hookeun Lee
Hyung-Kyoon Choi
Dong-Myung Kim
Choul-Gyun Lee
Suhyung Cho
Byung-Kwan Cho
author_facet Sang-Hyeok Cho
Yujin Jeong
Seong-Joo Hong
Hookeun Lee
Hyung-Kyoon Choi
Dong-Myung Kim
Choul-Gyun Lee
Suhyung Cho
Byung-Kwan Cho
author_sort Sang-Hyeok Cho
collection DOAJ
description ABSTRACT Cyanobacteria are promising industrial platforms owing to their ability to produce diverse natural secondary metabolites and nonnative value-added biochemicals from CO2 and light. To fully utilize their industrial potency, it is critical to understand their photosynthetic efficiency under various environmental conditions. In this study, we elucidated the inhibitory mechanisms of photosynthesis under high-light and low-temperature stress conditions in the model cyanobacterium Synechocystis sp. PCC 6803. Under each stress condition, the transcript abundance and translation efficiency were measured using transcriptome sequencing (RNA-seq) and ribosome profiling, and the genome-wide transcription unit architecture was constructed by data integration of transcription start sites and transcript 3′-end positions obtained from differential RNA-seq and sequencing of 3′-ends (Term-seq), respectively. Our results suggested that the mode of photosynthesis inhibition differed between the two stress conditions; high light stress induced photodamage responses, while low temperature stress impaired the translation efficiency of photosynthesis-associated genes. In particular, poor translation of photosystem I resulted from ribosome stalling at the untranslated regions, affecting the overall photosynthetic yield under low temperature stress. Our comprehensive multiomics analysis with transcription unit architecture provides foundational information on photosynthesis for future industrial strain development. IMPORTANCE Cyanobacteria are a compelling biochemical production platform for their ability to propagate using light and atmospheric CO2 via photosynthesis. However, the engineering of strains is hampered by limited understanding of photosynthesis under diverse environmental conditions such as high-light and low-temperature stresses. Herein, we decipher the transcriptomic and translatomic responses of the photosynthetic efficiency to stress conditions using the integrative analysis of multiomic data generated by RNA-seq and ribosome profiling, respectively. Through the generated massive data, along with the guide of the genome-wide transcription unit architecture constructed by transcription start sites and transcript 3′-end positions, we identified the factors affecting photosynthesis at transcription, posttranscription, and translation levels. Importantly, the high-light stress induces photodamage responses, and the low-temperature stress cripples the translation efficiency of photosynthesis-associated genes. The resulting insights provide pivotal information for future cyanobacterial cell factories powered by the engineering toward robust photosynthesis ability.
first_indexed 2024-12-20T16:57:01Z
format Article
id doaj.art-45dfbf66bdc8410c803a02f7a1ee4992
institution Directory Open Access Journal
issn 2379-5077
language English
last_indexed 2024-12-20T16:57:01Z
publishDate 2021-12-01
publisher American Society for Microbiology
record_format Article
series mSystems
spelling doaj.art-45dfbf66bdc8410c803a02f7a1ee49922022-12-21T19:32:41ZengAmerican Society for MicrobiologymSystems2379-50772021-12-016610.1128/mSystems.00943-21Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory ConditionsSang-Hyeok Cho0Yujin Jeong1Seong-Joo Hong2Hookeun Lee3Hyung-Kyoon Choi4Dong-Myung Kim5Choul-Gyun Lee6Suhyung Cho7Byung-Kwan Cho8Department of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of KoreaDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of KoreaDepartment of Biological Engineering, Inha University, Incheon, Republic of KoreaInstitute of Pharmaceutical Research, College of Pharmacy, Gachon University, Incheon, Republic of KoreaCollege of Pharmacy, Chung-Ang University, Seoul, Republic of KoreaDepartment of Chemical Engineering and Applied Chemistry, Chungnam National University, Daejeon, Republic of KoreaDepartment of Biological Engineering, Inha University, Incheon, Republic of KoreaDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of KoreaDepartment of Biological Sciences, Korea Advanced Institute of Science and Technology, Daejeon, Republic of KoreaABSTRACT Cyanobacteria are promising industrial platforms owing to their ability to produce diverse natural secondary metabolites and nonnative value-added biochemicals from CO2 and light. To fully utilize their industrial potency, it is critical to understand their photosynthetic efficiency under various environmental conditions. In this study, we elucidated the inhibitory mechanisms of photosynthesis under high-light and low-temperature stress conditions in the model cyanobacterium Synechocystis sp. PCC 6803. Under each stress condition, the transcript abundance and translation efficiency were measured using transcriptome sequencing (RNA-seq) and ribosome profiling, and the genome-wide transcription unit architecture was constructed by data integration of transcription start sites and transcript 3′-end positions obtained from differential RNA-seq and sequencing of 3′-ends (Term-seq), respectively. Our results suggested that the mode of photosynthesis inhibition differed between the two stress conditions; high light stress induced photodamage responses, while low temperature stress impaired the translation efficiency of photosynthesis-associated genes. In particular, poor translation of photosystem I resulted from ribosome stalling at the untranslated regions, affecting the overall photosynthetic yield under low temperature stress. Our comprehensive multiomics analysis with transcription unit architecture provides foundational information on photosynthesis for future industrial strain development. IMPORTANCE Cyanobacteria are a compelling biochemical production platform for their ability to propagate using light and atmospheric CO2 via photosynthesis. However, the engineering of strains is hampered by limited understanding of photosynthesis under diverse environmental conditions such as high-light and low-temperature stresses. Herein, we decipher the transcriptomic and translatomic responses of the photosynthetic efficiency to stress conditions using the integrative analysis of multiomic data generated by RNA-seq and ribosome profiling, respectively. Through the generated massive data, along with the guide of the genome-wide transcription unit architecture constructed by transcription start sites and transcript 3′-end positions, we identified the factors affecting photosynthesis at transcription, posttranscription, and translation levels. Importantly, the high-light stress induces photodamage responses, and the low-temperature stress cripples the translation efficiency of photosynthesis-associated genes. The resulting insights provide pivotal information for future cyanobacterial cell factories powered by the engineering toward robust photosynthesis ability.https://journals.asm.org/doi/10.1128/mSystems.00943-21cyanobacteriaSynechocystisphotosynthesistranscriptometranslatome
spellingShingle Sang-Hyeok Cho
Yujin Jeong
Seong-Joo Hong
Hookeun Lee
Hyung-Kyoon Choi
Dong-Myung Kim
Choul-Gyun Lee
Suhyung Cho
Byung-Kwan Cho
Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
mSystems
cyanobacteria
Synechocystis
photosynthesis
transcriptome
translatome
title Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
title_full Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
title_fullStr Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
title_full_unstemmed Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
title_short Different Regulatory Modes of Synechocystis sp. PCC 6803 in Response to Photosynthesis Inhibitory Conditions
title_sort different regulatory modes of synechocystis sp pcc 6803 in response to photosynthesis inhibitory conditions
topic cyanobacteria
Synechocystis
photosynthesis
transcriptome
translatome
url https://journals.asm.org/doi/10.1128/mSystems.00943-21
work_keys_str_mv AT sanghyeokcho differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT yujinjeong differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT seongjoohong differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT hookeunlee differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT hyungkyoonchoi differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT dongmyungkim differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT choulgyunlee differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT suhyungcho differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions
AT byungkwancho differentregulatorymodesofsynechocystissppcc6803inresponsetophotosynthesisinhibitoryconditions