Abstract

The Heterokonta or Stramenopile phylum comprises clades of unicellular photosynthetic species, which are promising for a broad range of biotechnological applications, based on their capacity to capture atmospheric CO2 via photosynthesis and produce biomolecules of interest. These molecules include triacylglycerol (TAG) loaded inside specific cytosolic bodies, called the lipid droplets (LDs). Understanding TAG production and LD biogenesis and function in photosynthetic stramenopiles is therefore essential, and is mostly based on the study of a few emerging models, such as the pennate diatom Phaeodactylum tricornutum and eustigmatophytes, such as Nannochloropsis and Microchloropsis species. The biogenesis of cytosolic LD usually occurs at the level of the endoplasmic reticulum. However, stramenopile cells contain a complex plastid deriving from a secondary endosymbiosis, limited by four membranes, the outermost one being connected to the endomembrane system. Recent cell imaging and proteomic studies suggest that at least some cytosolic LDs might be associated to the surface of the complex plastid, via still uncharacterized contact sites. The carbon length and number of double bonds of the acyl groups contained in the TAG molecules depend on their origin. De novo synthesis produces long-chain saturated or monounsaturated fatty acids (SFA, MUFA), whereas subsequent maturation processes lead to very long-chain polyunsaturated FA (VLC-PUFA). TAG composition in SFA, MUFA, and VLC-PUFA reflects therefore the metabolic context that gave rise to the formation of the LD, either via an early partitioning of carbon following FA de novo synthesis and/or a recycling of FA from membrane lipids, e.g., plastid galactolipids or endomembrane phosphor- or betaine lipids. In this review, we address the relationship between cytosolic LDs and the complex membrane compartmentalization within stramenopile cells, the metabolic routes leading to TAG accumulation, and the physiological conditions that trigger LD production, in response to various environmental factors.

Highlights

  • Stramenopiles, known as heterokonts, are a very large and diverse phylum (Derelle et al, 2016)

  • We summarize the current knowledge on the relationship between cytosolic lipid droplets (LDs) and the complex membrane compartmentalization within stramenopile cells, the metabolic routes leading to TAG accumulation, and the physiological conditions in which LDs are produced, in response to various environmental factors

  • Lipid Droplet Biogenesis Steps Stepwise LD formation has been mostly described in nonphotosynthetic organisms (Walther et al, 2017; Nettebrock and Bohnert, 2020; Renne et al, 2020) even though recent review articles have underlined some specificities of plastid-containing organisms (Chapman et al, 2019; Ischebeck et al, 2020; Leyland et al, 2020a)

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Summary

Lipid Droplets in Unicellular Photosynthetic Stramenopiles

The Heterokonta or Stramenopile phylum comprises clades of unicellular photosynthetic species, which are promising for a broad range of biotechnological applications, based on their capacity to capture atmospheric CO2 via photosynthesis and produce biomolecules of interest. These molecules include triacylglycerol (TAG) loaded inside specific cytosolic bodies, called the lipid droplets (LDs). We address the relationship between cytosolic LDs and the complex membrane compartmentalization within stramenopile cells, the metabolic routes leading to TAG accumulation, and the physiological conditions that trigger LD production, in response to various environmental factors

INTRODUCTION
The Origin of Secondary Plastids in Stramenopiles
Stepwise Formation of Lipid Droplet Subpopulations in Phaeodactylum
LIPID DROPLET FORMATION IN RESPONSE TO NITROGEN AND PHOSPHATE STARVATION
An Intense Lipid Remodeling Is Triggered Upon Nitrogen or Phosphate Starvation
Identification of Major Structural Lipid Droplet Proteins
Getting Ready to Recover From Stress
CONCLUDING REMARKS
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