Chlamydomonas mutants lacking chloroplast TRIOSE PHOSPHATE TRANSPORTER3 are metabolically compromised and light sensitive

Author:

Huang Weichao1ORCID,Krishnan Anagha2ORCID,Plett Anastasija3ORCID,Meagher Michelle4ORCID,Linka Nicole3ORCID,Wang Yongsheng15ORCID,Ren Bijie1ORCID,Findinier Justin1ORCID,Redekop Petra1ORCID,Fakhimi Neda1ORCID,Kim Rick G1ORCID,Karns Devin A2ORCID,Boyle Nanette4ORCID,Posewitz Matthew C2ORCID,Grossman Arthur R1ORCID

Affiliation:

1. Department of Plant Biology, Carnegie Institution for Science , Stanford, CA 94305 , USA

2. Department of Chemistry, Colorado School of Mines , Golden, CO 80401 , USA

3. Institute of Plant Biochemistry, Heinrich-Heine University Düsseldorf , 40225 Düsseldorf , Germany

4. Department of Chemical and Biological Engineering, Colorado School of Mines , Golden, CO 80401 , USA

5. School of Life Sciences, Tsinghua University , 100084 Beijing , China

Abstract

Abstract Modulation of photoassimilate export from the chloroplast is essential for controlling the distribution of fixed carbon in the cell and maintaining optimum photosynthetic rates. In this study, we identified chloroplast TRIOSE PHOSPHATE/PHOSPHATE TRANSLOCATOR 2 (CreTPT2) and CreTPT3 in the green alga Chlamydomonas (Chlamydomonas reinhardtii), which exhibit similar substrate specificities but whose encoding genes are differentially expressed over the diurnal cycle. We focused mostly on CreTPT3 because of its high level of expression and the severe phenotype exhibited by tpt3 relative to tpt2 mutants. Null mutants for CreTPT3 had a pleiotropic phenotype that affected growth, photosynthetic activities, metabolite profiles, carbon partitioning, and organelle-specific accumulation of H2O2. These analyses demonstrated that CreTPT3 is a dominant conduit on the chloroplast envelope for the transport of photoassimilates. In addition, CreTPT3 can serve as a safety valve that moves excess reductant out of the chloroplast and appears to be essential for preventing cells from experiencing oxidative stress and accumulating reactive oxygen species, even under low/moderate light intensities. Finally, our studies indicate subfunctionalization of the TRIOSE PHOSPHATE/PHOSPHATE TRANSLOCATOR (CreTPT) transporters and suggest that there are differences in managing the export of photoassimilates from the chloroplasts of Chlamydomonas and vascular plants.

Funder

DOE

US Department of Energy

Office of Science

Basic Energy Systems

Office of Biological and Environmental Research

German Research Foundations

National Science Foundation

Carnegie Institution for Science

Human Frontier Science Program

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science

Cited by 11 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3