Journal Article
- Identification of trehalose as a compatible solute in different species of acidophilic bacteria
-
Pedro A. Galleguillos , Barry M. Grail , Kevin B. Hallberg , Cecilia S. Demergasso , D. Barrie Johnson
-
J. Microbiol. 2018;56(10):727-733. Published online September 28, 2018
-
DOI: https://doi.org/10.1007/s12275-018-8176-2
-
-
49
View
-
0
Download
-
19
Crossref
-
Abstract
-
The major industrial heap bioleaching processes are located
in desert regions (mainly Chile and Australia) where fresh
water is scarce and the use of resources with low water activity
becomes an attractive alternative. However, in spite
of the importance of the microbial populations involved in
these processes, little is known about their response or adaptation
to osmotic stress. In order to investigate the response
to osmotic stress in these microorganisms, six species of acidophilic
bacteria were grown at elevated osmotic strength in
liquid media, and the compatible solutes synthesised were
identified using ion chromatography and MALDI-TOF mass
spectrometry. Trehalose was identified as one of, or the sole,
compatible solute in all species and strains, apart from Acidithiobacillus
thiooxidans where glucose and proline levels
increased at elevated osmotic potentials. Several other potential
compatible solutes were tentatively identified by MALDITOF
analysis. The same compatible solutes were produced
by these bacteria regardless of the salt used to produce the osmotic
stress. The results correlate with data from sequenced
genomes which confirm that many chemolithotrophic and
heterotrophic acidophiles possess genes for trehalose synthesis.
This is the first report to identify and quantify compatible
solutes in acidophilic bacteria that have important
roles in biomining technologies.
-
Citations
Citations to this article as recorded by

- Improvement in Salt Tolerance Ability of Pseudomonas putida KT2440
Min Fan, Shuyu Tan, Wei Wang, Xuehong Zhang
Biology.2024; 13(6): 404. CrossRef - A novel strategy for Klebsiella sp. to resist high salt and high phenol environmental stress
Jiejing Zhang, Chong Hu, Yu Wu, Jing Liang, Cesar Danilo Valle Exposito, Jianfeng Zhang
Process Biochemistry.2024; 146: 316. CrossRef - Multi-stress adaptive lifestyle of acidophiles enhances their robustness for biotechnological and environmental applications
Godwin O. Aliyu, Flora N. Ezugworie, Chukwudi O. Onwosi, Chukwudi I. Nnamchi, Chito C. Ekwealor, Victor C. Igbokwe, Rajesh K. Sani
Science of The Total Environment.2024; 954: 176190. CrossRef - Osmotic response in Leptospirillum ferriphilum isolated from an industrial copper bioleaching environment to sulfate
Dayana Arias, Víctor Zepeda, Ivan Nancucheo, Manuel Saldaña, Pedro A. Galleguillos
Frontiers in Microbiology.2024;[Epub] CrossRef - Interplay between desiccation and oxidative stress responses in iron-oxidizing acidophilic bacteria
Muñoz-Villagrán Claudia, Acevedo-Arbunic Javiera, Navarro-Salazar Sebastián, Fuentes-Rubio José, Levicán Gloria
Journal of Biotechnology.2024; 383: 64. CrossRef - Study on the intracellular adaptative mechanism of Acidithiobacillus caldus MTH-04 to NaCl stress
Min Li, Jianping Wen
Microbial Cell Factories.2023;[Epub] CrossRef - New Features of Acidophilic Bacteria of the Genus Sulfobacillus: Polysaccharide Biosynthesis and Degradation Pathways
Anna Panyushkina, Maxim Muravyov
Minerals.2023; 13(2): 255. CrossRef -
Salinity changes the nitrification activity and community composition of comammox
Nitrospira
in intertidal sediments of Yangtze River estuary
Ran Jiang, Wen-Jing Qin, Ru-Yi Zhang, Kai Zhang, Xing Huang, Yong Li, Chen-Hao Zhou, Ting Zhu, Yan Zhang, Bin Zou, Ming Nie, Sung-Keun Rhee, Zhe-Xue Quan, Nick Bouskill
mSystems.2023;[Epub] CrossRef - Analysis of carbohydrates and glycoconjugates by matrix‐assisted laser desorption/ionization mass spectrometry: An update for 2017–2018
David J. Harvey
Mass Spectrometry Reviews.2023; 42(1): 227. CrossRef - Eurypsychrophilic acidophiles: From (meta)genomes to low-temperature biotechnologies
Mark Dopson, Carolina González-Rosales, David S. Holmes, Nadia Mykytczuk
Frontiers in Microbiology.2023;[Epub] CrossRef - Reduction of greenhouse gas (GHG) emission in the vegetation-activated sludge process (V-ASP) involving decontaminated plants for decentralized wastewater treatment
Jian-Jiang Lu, Zi-Jun Dong, Pu Li, Wei-Jia Yan, Jia-Jia Yuan, Wen-Yi Dong, Fei-Yun Sun, Yun-Xian Shao
Journal of Cleaner Production.2022; 362: 132341. CrossRef - Identification of novel halophilic/halotolerant bacterial species producing compatible solutes
Furkan Orhan, Ertuğrul Ceyran
International Microbiology.2022; 26(2): 219. CrossRef - Transcriptomic analysis of chloride tolerance in Leptospirillum ferriphilum DSM 14647 adapted to NaCl
Javier Rivera-Araya, Thomas Heine, Renato Chávez, Michael Schlömann, Gloria Levicán, Benjamin J. Koestler
PLOS ONE.2022; 17(4): e0267316. CrossRef - Glutathione Synthetase Overexpression in Acidithiobacillus ferrooxidans Improves Halotolerance of Iron Oxidation
Yuta Inaba, Alan C. West, Scott Banta, Robert M. Kelly
Applied and Environmental Microbiology.2021;[Epub] CrossRef - Examining the Osmotic Response of Acidihalobacter aeolianus after Exposure to Salt Stress
Melissa K. Corbett, Liam Anstiss, April Gifford, Ross M. Graham, Elizabeth L. J. Watkin
Microorganisms.2021; 10(1): 22. CrossRef - From Laboratory towards Industrial Operation: Biomarkers for Acidophilic Metabolic Activity in Bioleaching Systems
Sabrina Marín, Mayra Cortés, Mauricio Acosta, Karla Delgado, Camila Escuti, Diego Ayma, Cecilia Demergasso
Genes.2021; 12(4): 474. CrossRef - Mechanisms of NaCl-tolerance in acidophilic iron-oxidizing bacteria and archaea: Comparative genomic predictions and insights
Javier Rivera-Araya, Ngoc Dieu Huynh, Marek Kaszuba, Renato Chávez, Michael Schlömann, Gloria Levicán
Hydrometallurgy.2020; 194: 105334. CrossRef - Osmotic Imbalance, Cytoplasm Acidification and Oxidative Stress Induction Support the High Toxicity of Chloride in Acidophilic Bacteria
Javier Rivera-Araya, Andre Pollender, Dieu Huynh, Michael Schlömann, Renato Chávez, Gloria Levicán
Frontiers in Microbiology.2019;[Epub] CrossRef - Uncovering the Mechanisms of Halotolerance in the Extremely Acidophilic Members of the Acidihalobacter Genus Through Comparative Genome Analysis
Himel N. Khaleque, Carolina González, Raihan Shafique, Anna H. Kaksonen, David S. Holmes, Elizabeth L. J. Watkin
Frontiers in Microbiology.2019;[Epub] CrossRef
Research Support, Non-U.S. Gov't
- Identification and Characterization of Ectoine Biosynthesis Genes and Heterologous Expression of the ectABC Gene Cluster from Halomonas sp. QHL1, a Moderately Halophilic Bacterium Isolated from Qinghai Lake
-
Derui Zhu , Jian Liu , Rui Han , Guoping Shen , Qifu Long , Xiaoxing Wei , Deli Liu
-
J. Microbiol. 2014;52(2):139-147. Published online February 1, 2014
-
DOI: https://doi.org/10.1007/s12275-014-3389-5
-
-
45
View
-
0
Download
-
16
Crossref
-
Abstract
-
The moderately halophilic bacterium Halomonas sp. QHL1 was identified as a member of the genus Halomonas by 16S rRNA gene sequencing. HPLC analysis showed that strain QHL1 synthesizes ectoine in its cytoplasm. The genes involved in the ectoine biosynthesis pathway were identified on the chromosome in the order ectABC. Subsequently, the ectB gene from this strain was amplified by PCR, and the entire ectABC gene cluster (3,580 bp) was cloned using genome walking. Analysis showed that the ectA (579 bp), ectB (1269 bp), and ectC (390 bp) genes were organized in a single transcriptional unit and were predicted to encode three peptides of 21.2 kDa, 46.4 kDa, and 14.7 kDa, respectively. Two putative promoters, a δ70-dependent promoter and a δ38-controlled promoter, as well as several conserved motifs with unknown function were identified. Individual ectA, ectB, and ectC genes, and the entire ectABC gene cluster were inserted into the expression plasmid pET-28a(+) to generate the recombinant plasmids pET-28a(+)-ectA, pET-28a(+)-ectB, pET-28a(+)-ectC and pET-28a(+)-ectABC, respectively. Heterologous expression of these proteins in Escherichia coli BL21 (DE3) was confirmed by SDS-PAGE. The recombinant E. coli strain BL21 (pET-28a (+)-ectABC) displayed a higher salt tolerance than native E. coli cells but produced far less ectoine than the wild-type QHL1 strain.
-
Citations
Citations to this article as recorded by

- Biotechnological production of ectoine: current status and prospects
Jun Chen, Deliang Qiao, Tao Yuan, Yeyuan Feng, Pengjun Zhang, Xuejun Wang, Li Zhang
Folia Microbiologica.2024; 69(2): 247. CrossRef - Comparative genomic analysis of Halomonas campaniensis wild-type and ultraviolet radiation-mutated strains reveal genomic differences associated with increased ectoine production
Zhibo Wang, Yongzhen Li, Xiang Gao, Jiangwa Xing, Rong Wang, Derui Zhu, Guoping Shen
International Microbiology.2023; 26(4): 1009. CrossRef - Comparative Genome Analysis of a Novel Alkaliphilic Actinobacterial Species Nesterenkonia haasae
Shuang Wang, Lei Sun, Manik Prabhu Narsing Rao, Bao‑zhu Fang, Wen‑jun Li
Polish Journal of Microbiology.2022; 71(3): 453. CrossRef - Whole genome sequencing of the halophilic Halomonas qaidamensis XH36, a novel species strain with high ectoine production
Tiantian Zhang, Tianqi Cui, Yaning Cao, Yongzhen Li, Fenghui Li, Derui Zhu, Jiangwa Xing
Antonie van Leeuwenhoek.2022; 115(4): 545. CrossRef - Identification and characterization of an ectoine biosynthesis gene cluster from Aestuariispira ectoiniformans sp. nov., isolated from seawater
Ji Young Kang, Binna Lee, Jeong Ah Kim, Min-Soo Kim, Chul Ho Kim
Microbiological Research.2022; 254: 126898. CrossRef -
Genome Sequence of
Streptomyces
sp. Strain GQFP Isolated from Soil Near the Roots of Pharmaceutical Plant Elaeagnus pungens
Jie Zhu, David A. Baltrus
Microbiology Resource Announcements.2022;[Epub] CrossRef - Enhanced production of ectoine from methane using metabolically engineered Methylomicrobium alcaliphilum 20Z
Sukhyeong Cho, Yun Seo Lee, Hanyu Chai, Sang Eun Lim, Jeong Geol Na, Jinwon Lee
Biotechnology for Biofuels and Bioproducts.2022;[Epub] CrossRef - Ectoine Production Using Novel Heterologous EctABCS. salarius from Marine Bacterium Salinicola salarius
Yue Su, Wenting Peng, Tong Wang, Yanhui Li, Luyu Zhao, Xinyu Wang, Ying Li, Ling Lin
Applied Sciences.2021; 11(15): 6873. CrossRef - High ectoine production by an engineered Halomonas hydrothermalis Y2 in a reduced salinity medium
Qi Zhao, Shannan Li, Peiwen Lv, Simian Sun, Cuiqing Ma, Ping Xu, Haijun Su, Chunyu Yang
Microbial Cell Factories.2019;[Epub] CrossRef - Analysis of Zobellella denitrificans ZD1 draft genome: Genes and gene clusters responsible for high polyhydroxybutyrate (PHB) production from glycerol under saline conditions and its CRISPR-Cas system
Yu-Wei Wu, Shih-Hung Yang, Myung Hwangbo, Kung-Hui Chu, Chih-Horng Kuo
PLOS ONE.2019; 14(9): e0222143. CrossRef - Engineering the Salt-Inducible Ectoine Promoter Region of Halomonas elongata for Protein Expression in a Unique Stabilizing Environment
Lisa Stiller, Erwin Galinski, Elisabeth Witt
Genes.2018; 9(4): 184. CrossRef - New Alpiniamides From Streptomyces sp. IB2014/011-12 Assembled by an Unusual Hybrid Non-ribosomal Peptide Synthetase Trans-AT Polyketide Synthase Enzyme
Constanze Paulus, Yuriy Rebets, Josef Zapp, Christian Rückert, Jörn Kalinowski, Andriy Luzhetskyy
Frontiers in Microbiology.2018;[Epub] CrossRef - Metabolic engineering of Escherichia coli for L-tryptophan production
V. B. Panichkin, V. A. Livshits, I. V. Biryukova, S. V. Mashko
Applied Biochemistry and Microbiology.2016; 52(9): 783. CrossRef -
Draft Genome Sequence of Halomonas elongata Strain K4, an Endophytic Growth-Promoting Bacterium Enhancing Salinity Tolerance
In Planta
Feras F. Lafi, Juan S. Ramirez-Prado, Intikhab Alam, Vladimir B. Bajic, Heribert Hirt, Maged M. Saad
Genome Announcements.2016;[Epub] CrossRef - High production of ectoine from aspartate and glycerol by use of whole-cell biocatalysis in recombinant Escherichia coli
Yong-Zhi He, Jiao Gong, Hai-Ying Yu, Yong Tao, Shan Zhang, Zhi-Yang Dong
Microbial Cell Factories.2015;[Epub] CrossRef - Design of an ectoine-responsive AraC mutant and its application in metabolic engineering of ectoine biosynthesis
Wei Chen, Shan Zhang, Peixia Jiang, Jun Yao, Yongzhi He, Lincai Chen, Xiwu Gui, Zhiyang Dong, Shuang-Yan Tang
Metabolic Engineering.2015; 30: 149. CrossRef