Abstract

Microalgae are unicellular photosynthetic organisms considered as potential alternative sources for biomass, biofuels or high value products. However, limited biomass productivity is commonly experienced in their cultivating system despite their high potential. One of the reasons for this limitation is the high thermal dissipation of the light absorbed by the outer layers of the cultures exposed to high light caused by the activation of a photoprotective mechanism called non-photochemical quenching (NPQ). In the model organism for green algae Chlamydomonas reinhardtii, NPQ is triggered by pigment binding proteins called light-harvesting-complexes-stress-related (LHCSRs), which are over-accumulated in high light. It was recently reported that biomass productivity can be increased both in microalgae and higher plants by properly tuning NPQ induction. In this work increased light use efficiency is reported by introducing in C. reinhardtii a LHCSR3 gene under the control of Heat Shock Protein 70/RUBISCO small chain 2 promoter in a npq4 lhcsr1 background, a mutant strain knockout for all LHCSR genes. This complementation strategy leads to a low expression of LHCSR3, causing a strong reduction of NPQ induction but is still capable of protecting from photodamage at high irradiance, resulting in an improved photosynthetic efficiency and higher biomass accumulation.

Highlights

  • Photosynthetic organisms convert light energy into chemical energy to be used for carbon fixation to sustain cellular metabolism

  • These results suggested that it is possible to improve biomass production in C. reinhardtii reducing non-photochemical quenching (NPQ) activation if a basal level of photoprotection is ensured by accumulation of some light-harvesting-complexes- stress-related (LHCSRs) subunits, such as LHCSR1 in the case of npq4 mutant [20]

  • A different strategy to obtain strains with reduced NPQ and increased photosynthetic efficiency was addressed, by complementation of npq4 lhcsr1 mutant with LHCSR3 gene under control of a promoter obtained by fusion of Heat Shock Protein (HSP)70 and RUBISCO small subunit (RBCS) 2 promoters [35]: LHCSR3 gene controlled by HSP70/RBCS2 promoter is not strongly induced in high light resulting in a low expression of this gene and reduced NPQ compared to WT

Read more

Summary

Introduction

Photosynthetic organisms convert light energy into chemical energy to be used for carbon fixation to sustain cellular metabolism. In the model organism for green algae, Chlamydomonas reinhardtii, NPQ is triggered by the pigment-binding subunits LHCSR1 and LHCSR3, two LHC (light harvesting complex)-like Chl a/b-xanthophyll-binding proteins; these subunits have been reported to trigger NPQ induction on the basis of lumenal pH, being able to significantly quench excitation energy present at the level of both PSI and PSII [15,20,28,29,30,31] Both genes for LHCSR1 and LHCSR3 are transcriptionally regulated causing overaccumulation of these subunits in stress conditions [15,32]. This strategy could be required for the biotechnological manipulation of other microalgae species inducing a basal accumulation of LHCSR subunits in mutants with NPQ phenotypes

Complementation of npq4 lhcsr1 Strain
NPQ Induction and LHCSR3 Accumulation
Biomass Productivity Transformed lines with
Chlamydomonas Reinhardtii Transformation
Chlamydomonas Reinhardtii Cultivation
Chlorophyll Fluorescence and Oxygen Evolution Measurement
Pigment Analysis
Singlet Oxygen Production
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call