» Articles » PMID: 28655777

Monogalactosyldiacylglycerol Facilitates Synthesis of Photoactive Protochlorophyllide in Etioplasts

Overview
Journal Plant Physiol
Specialty Physiology
Date 2017 Jun 29
PMID 28655777
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

Cotyledon cells of dark-germinated angiosperms develop etioplasts that are plastids containing unique internal membranes called prolamellar bodies (PLBs). Protochlorophyllide (Pchlide), a precursor of chlorophyll, accumulates in PLBs and forms a ternary complex with NADPH and light-dependent NADPH:protochlorophyllide oxidoreductase (LPOR), which allows for the rapid formation of chlorophyll after illumination while avoiding photodamage. PLBs are 3D lattice structures formed by the lipid bilayer rich in monogalactosyldiacylglycerol (MGDG). Although MGDG was found to be required for the formation and function of the thylakoid membrane in chloroplasts in various plants, the roles of MGDG in PLB formation and etioplast development are largely unknown. To analyze the roles of MGDG in etioplast development, we suppressed encoding the major isoform of MGDG synthase by using a dexamethasone-inducible artificial microRNA in etiolated Arabidopsis () seedlings. Strong suppression caused a 36% loss of MGDG in etiolated seedlings, together with a 41% decrease in total Pchlide content. The loss of MGDG perturbed etioplast membrane structures and impaired the formation of the photoactive Pchlide-LPOR-NADPH complex and its oligomerization, without affecting LPOR accumulation. The suppression also impaired the formation of Pchlide from protoporphyrin IX via multiple enzymatic reactions in etioplast membranes, which suggests that MGDG is required for the membrane-associated processes in the Pchlide biosynthesis pathway. Suppressing at several germination stages revealed that MGDG biosynthesis at an early germination stage is particularly important for Pchlide accumulation. MGDG biosynthesis may provide a lipid matrix for Pchlide biosynthesis and the formation of Pchlide-LPOR complexes as an initial step of etioplast development.

Citing Articles

Light dependent protochlorophyllide oxidoreductase: a succinct look.

Vedalankar P, Tripathy B Physiol Mol Biol Plants. 2024; 30(5):719-731.

PMID: 38846463 PMC: 11150229. DOI: 10.1007/s12298-024-01454-5.


Orchestration of Photosynthesis-Associated Gene Expression and Galactolipid Biosynthesis during Chloroplast Differentiation in Plants.

Fujii S, Wada H, Kobayashi K Plant Cell Physiol. 2024; 65(6):1014-1028.

PMID: 38668647 PMC: 11209550. DOI: 10.1093/pcp/pcae049.


Anionic lipids facilitate membrane development and protochlorophyllide biosynthesis in etioplasts.

Yoshihara A, Kobayashi K, Nagata N, Fujii S, Wada H, Kobayashi K Plant Physiol. 2023; 194(3):1692-1704.

PMID: 37962588 PMC: 10904342. DOI: 10.1093/plphys/kiad604.


Comparative changes in sugars and lipids show evidence of a critical node for regeneration in safflower seeds during aging.

Zhou L, Lu L, Chen C, Zhou T, Wu Q, Wen F Front Plant Sci. 2022; 13:1020478.

PMID: 36388552 PMC: 9661361. DOI: 10.3389/fpls.2022.1020478.


Enhanced Adaptability to Limited Water Supply Regulated by Diethyl Aminoethyl Hexanoate (DA-6) Associated With Lipidomic Reprogramming in Two White Clover Genotypes.

Hassan M, Qi H, Cheng B, Hussain S, Peng Y, Liu W Front Plant Sci. 2022; 13:879331.

PMID: 35668812 PMC: 9163823. DOI: 10.3389/fpls.2022.879331.


References
1.
Schoefs B, Franck F . Protochlorophyllide reduction: mechanisms and evolutions. Photochem Photobiol. 2004; 78(6):543-57. DOI: 10.1562/0031-8655(2003)078<0543:prmae>2.0.co;2. View

2.
Solymosi K, Schoefs B . Etioplast and etio-chloroplast formation under natural conditions: the dark side of chlorophyll biosynthesis in angiosperms. Photosynth Res. 2010; 105(2):143-66. DOI: 10.1007/s11120-010-9568-2. View

3.
Wang P, Grimm B . Organization of chlorophyll biosynthesis and insertion of chlorophyll into the chlorophyll-binding proteins in chloroplasts. Photosynth Res. 2015; 126(2-3):189-202. DOI: 10.1007/s11120-015-0154-5. View

4.
Pogson B, Woo N, Forster B, Small I . Plastid signalling to the nucleus and beyond. Trends Plant Sci. 2008; 13(11):602-9. DOI: 10.1016/j.tplants.2008.08.008. View

5.
Kopetz K, Kolossov V, Rebeiz C . Chloroplast biogenesis 89: development of analytical tools for probing the biosynthetic topography of photosynthetic membranes by determination of resonance excitation energy transfer distances separating metabolic tetrapyrrole donors from.... Anal Biochem. 2004; 329(2):207-19. DOI: 10.1016/j.ab.2004.03.008. View