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
-
-
59
View
-
0
Download
-
21
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

- Adaptive response of the holdase chaperone network of Acidithiobacillus ferrooxidans ATCC 23270 to stresses and energy sources
Katherin Izquierdo-Fiallo, Claudia Muñoz-Villagrán, Christian Schimpf, Mick Parra Mardonez, David Rafaja, Michael Schlömann, Mario Tello, Omar Orellana, Gloria Levicán
World Journal of Microbiology and Biotechnology.2025;[Epub] CrossRef - Deciphering hypersaline tolerance mechanism of the pyridine-degrading strain Rhodococcus sp. PD10
Yangfan Hu, Zhichun Wang, Zizhen Liu, Korakot Sombatmankhong, Bo Yu
Environmental Technology & Innovation.2025; 38: 104168. CrossRef - 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
- Complete Genome of Leptospirillum ferriphilum ML-04 Provides Insight into Its Physiology and Environmental Adaptation
-
Shuang Mi , Jian Song , Jianqun Lin , Yuanyuan Che , Huajun Zheng , Jianqiang Lin
-
J. Microbiol. 2011;49(6):890-901. Published online December 28, 2011
-
DOI: https://doi.org/10.1007/s12275-011-1099-9
-
-
38
View
-
0
Download
-
49
Scopus
-
Abstract
-
Leptospirillum ferriphilum has been identified as the dominant, moderately thermophilic, bioleaching microorganism in bioleaching processes. It is an acidic and chemolithoautrophic bacterium that gains electrons from ferrous iron oxidation for energy production and cell growth. Genetic information about this microorganism has been limited until now, which has hindered its further exploration. In this study, the complete genome of L. ferripilum ML-04 is sequenced and annotated. The bacterium has a single circular chromosome of 2,406,157 bp containing 2,471 coding sequences (CDS), 2 rRNA operons, 48 tRNA genes, a large number of mobile genetic elements and 2 genomic islands. In silico analysis shows L. ferriphilum ML-04 fixes carbon through a reductive citric acid (rTCA) cycle, and obtains nitrogen through ammonium assimilation. The genes related to “cell envelope biogenesis, outer membrane” (6.9%) and “DNA replication, recombination and repair” (5.6%) are abundant, and a large number of genes related to heavy metal detoxification, oxidative and acidic stress defense, and signal transduction pathways were detected. The genomic plasticity, plentiful cell envelope components, inorganic element metabolic abilities and stress response mechanisms found the base for this organism’s survival in the bioleaching niche.