» Articles » PMID: 33214980

The Saltern-derived DSM 102817 is a New High-yield Ectoines Producer in Minimal Medium and Under Salt Stress Conditions

Overview
Journal 3 Biotech
Publisher Springer
Specialty Biotechnology
Date 2020 Nov 20
PMID 33214980
Citations 2
Authors
Affiliations
Soon will be listed here.
Abstract

In the present study, the growth conditions and accumulation of ectoines (ectoine and hydroxyectoine) by DSM 102817 under salt stress conditions have been investigated. The productivity assay of this strain for ectoines revealed that the highest cellular content was reached in the minimal glucose sea water medium (SW-15) within 15% salinity. The addition of 0.1% (w/v) aspartic acid to the medium allowed an average of four times higher biomass production, and a dry mycelial biomass of 1.76 g L was obtained after 6 days of growth in shake flasks at 40 °C and 200 rpm. Among the inorganic cations supplemented to the glucose SW-15 medium, the addition of 1 mM Fe yielded the highest amount of mycelial biomass (3.45 g L) and total ectoines content (119 mg g), resulting in about 410 mg L of products at the end of exponential growth phase. After 1 h of incubation in an osmotic downshock solution containing 2% NaCl, 70% of this content was released by the mycelium, and recovering cells maintained a high survival, with a maximal growth rate ( ) of about 93% of the control population exposed to 15% NaCl. During growth at optimal salinity and temperature (15% NaCl and 40 °C), developed a compact and circular pellets that were easy to separate by simple decantation from both fermentation media and after hypoosmotic shock. Overall, the ectoines excreting could be a promising resource for ectoines production in a commercially valuable culture medium and at a large-scale fermentation process.

Citing Articles

The family : an emerging microbial resource with high application value.

Zhong M, Sun Z, Wei C, Muhoza B, Tian H, Liu M Front Microbiol. 2025; 16:1507902.

PMID: 39935634 PMC: 11810901. DOI: 10.3389/fmicb.2025.1507902.


Whole genome sequencing of the halophilic Halomonas qaidamensis XH36, a novel species strain with high ectoine production.

Zhang T, Cui T, Cao Y, Li Y, Li F, Zhu D Antonie Van Leeuwenhoek. 2022; 115(4):545-559.

PMID: 35243586 DOI: 10.1007/s10482-022-01709-9.


Genome analysis of the salt-resistant Paludifilum halophilum DSM 102817 reveals genes involved in flux-tuning of ectoines and unexplored bioactive secondary metabolites.

Frikha-Dammak D, Ayadi H, Hakim-Rekik I, Belbahri L, Maalej S World J Microbiol Biotechnol. 2021; 37(10):178.

PMID: 34549358 DOI: 10.1007/s11274-021-03147-7.

References
1.
Frikha-Dammak D, Fardeau M, Cayol J, Ben Fguira-Fourati L, Najeh S, Ollivier B . Paludifilum halophilum gen. nov., sp. nov., a thermoactinomycete isolated from superficial sediment of a solar saltern. Int J Syst Evol Microbiol. 2016; 66(12):5371-5378. DOI: 10.1099/ijsem.0.001523. View

2.
He Y, Gong J, Yu H, Tao Y, Zhang S, Dong Z . High production of ectoine from aspartate and glycerol by use of whole-cell biocatalysis in recombinant Escherichia coli. Microb Cell Fact. 2015; 14:55. PMC: 4405841. DOI: 10.1186/s12934-015-0238-0. View

3.
Rani A, Venkatesu P . Changing relations between proteins and osmolytes: a choice of nature. Phys Chem Chem Phys. 2018; 20(31):20315-20333. DOI: 10.1039/c8cp02949k. View

4.
Argandona M, Nieto J, Iglesias-Guerra F, Calderon M, Garcia-Estepa R, Vargas C . Interplay between iron homeostasis and the osmotic stress response in the halophilic bacterium Chromohalobacter salexigens. Appl Environ Microbiol. 2010; 76(11):3575-89. PMC: 2876472. DOI: 10.1128/AEM.03136-09. View

5.
Pastor J, Salvador M, Argandona M, Bernal V, Reina-Bueno M, Csonka L . Ectoines in cell stress protection: uses and biotechnological production. Biotechnol Adv. 2010; 28(6):782-801. DOI: 10.1016/j.biotechadv.2010.06.005. View