Submerged membrane photobioreactor for the cultivation of Haslea ostrearia and the continuous extraction of extracellular marennine.

Nesrine Gargouch, Raphaelle Touchard, Hélène Marec, Jean Luc Mouget, Jérémy Pruvost, Anthony Massé
Author Information
  1. Nesrine Gargouch: Université de Nantes, Oniris, CNRS, GEPEA, UMR 6144, F-44600 Saint-Nazaire, France.
  2. Raphaelle Touchard: CAPACITÉS SAS, 26 Bd Vincent Gâche, 44200 Nantes, France.
  3. Hélène Marec: Université de Nantes, Oniris, CNRS, GEPEA, UMR 6144, F-44600 Saint-Nazaire, France.
  4. Jean Luc Mouget: Mer-Molécules-Santé, MMS, FR CNRS 3473, IUML, Le Mans Université, 72000 Le Mans, France.
  5. Jérémy Pruvost: Université de Nantes, Oniris, CNRS, GEPEA, UMR 6144, F-44600 Saint-Nazaire, France.
  6. Anthony Massé: Université de Nantes, Oniris, CNRS, GEPEA, UMR 6144, F-44600 Saint-Nazaire, France. Electronic address: anthony.masse@univ-nantes.fr.

Abstract

Haslea ostrearia is a marine diatom known to produce and excrete the marenine blue pigment. Its controlled, continuous and intensified cultivation remains a challenge. Thus, a submerged membrane photobioreactor (MPBR) was implemented in order to simultaneously and continuously cultivate H. ostrearia and extract marennine. The MPBR was compared with a similar air-lift photobioreactor (without membrane), both working at a dilution rate equal to 0.1, 0.3 and 0.5 d. Contrary to the air-lift photobioreactor, the MPBR successfully operated at high dilution rate without biomass washout. The MPBR allowed continuously recovering marennine and reaching high cell density (555 ± 25 × 10 cells L at D = 0.1 d), marennine concentration (36.00 ± 0.02 mg L at D = 0.1 d) and marenine productivity (7.20 ± 0.01 mg L d at D = 0.5 d).

Keywords

MeSH Term

Biomass
Diatoms
Phenols
Photobioreactors
Pigmentation

Chemicals

Phenols
marennine

Word Cloud

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