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Characterization of a salt-induced DhAHP, a gene coding for alkyl hydroperoxide reductase, from the extremely halophilic yeast Debaryomyces hansenii
© Chao et al; licensee BioMed Central Ltd. 2009
- Received: 2 March 2009
- Accepted: 28 August 2009
- Published: 28 August 2009
Debaryomyces hansenii is one of the most salt tolerant species of yeast and has become a model organism for the study of tolerance mechanisms against salinity. The goal of this study was to identify key upregulated genes that are involved in its adaptation to high salinity.
By using forward subtractive hybridization we have cloned and sequenced DhAHP from D. hansenii that is significantly upregulated during salinity stress. DhAHP is orthologous to the alkly hydroperoxide reductase of the peroxiredoxin gene family, which catalyzes the reduction of peroxides at the expense of thiol compounds. The full-lengthed cDNA of DhAHP has 674 bp of nucleotide and contains a 516 bp open reading frame (ORF) encoding a deduced protein of 172 amino acid residues (18.3 kDa). D. hansenii Ahp is a cytosolic protein that belongs to the Ahp of the 1-Cys type peroxiredoxins. Phylogentically, the DhAhp and Candida albicans Ahp11 (Swiss-Prot: Q5AF44) share a common ancestry but show divergent evolution. Silence of its expression in D. hansenii by RNAi resulted in decreased tolerance to salt whereas overexpression of DhAHP in D. hansenii and the salt-sensitive yeasts Saccharomyces cereviasiae and Pichia methanolica conferred a higher tolerance with a reduced level of reactive oxygen species.
In conclusion, for the first time our study has identified alkly hydroperoxide reductase as a key protein involved in the salt tolerance of the extremely halophilic D. hansenii. Apparently, this enzyme plays a multi-functional role in the yeast's adaptation to salinity; it serves as a peroxidase in scavenging reactive oxygen species, as a molecular chaperone in protecting essential proteins from denaturation, and as a redox sensor in regulating H2O2-mediated cell defense signaling.
- Reactive Oxygen Species
- Wild Type Strain
- Salt Tolerance
- Subtract cDNA Library
- Shewanella Putrefaciens
Debaryomyces hansenii is an ascomycetous salt- and high pH-tolerant yeast that has been defined as halotolerant or halophilic . It was isolated from saline environments such as sea water  or concentrated brines , representing one of the most salt tolerant species of yeasts. This marine yeast can tolerate salinity levels up to 24% (4.11 M) of NaCl . In contrast, growth of the Baker's yeast Saccharomyces cerevisiae is severely inhibited when salinity reaches 10% NaCl . Thus, D. hansenii has become a model organism for the study of salt tolerance mechanisms in eukaryotic cells . It is now well recognized that the mechanisms by which all organisms achieve osmotic and ionic equilibrium are mediated by orthologous mechanisms based on conserved biochemical and/or physiological functions that are inherently necessary for essential metabolic processes .
Under saline conditions, D. hansenii accumulates large amounts of Na+ without being intoxicated even when K+ is present at low concentration in the environment . In fact, Na+ improves growth and protects D. hansenii in the presence of additional stress factors . For example, at high or low temperature and extreme pH growth of the yeast is improved by the presence of 1 M NaCl . It has been clearly shown that sodium ions are less toxic for D. hansenii as compared with other organisms; therefore, it is considered a 'sodium-includer' organism . The reduced toxic effect by Na+ and its accumulation at high levels under high salt is probably indicative of an adaptive strategy of D. hansenii for growth in hypersaline environments . The organism must posses an array of advantageous characteristics that collectively confer its high halotolerance. Earlier studies have identified a number of salt-related genes in the extreme halophilic yeast D. hansenii, such as HOG1 (MAP kinase involved in high-osmolarity glycerol synthesis pathway) , ENA1 and ENA2 (plasmamembrane Na+-ATPase , GPD1 and GPP (NAD-glycerol-3-phosphate dehydrogenase and glycerol-3-phosphatase) , NHX1 (vacuolar Na+ antiporter)  and KHA1 (Na+/H+ antiporter) . As expected, most of these salt-upregulated genes are involved in osmoregulation or transport of ions. However, the collective underlying mechanisms by which D. hansenii tolerates high levels of NaCl remain unkown.
All aerobic organisms require oxygen for efficient production of energy, but at the same time the organisms are constantly exposed to oxidative stress. This can be caused by partially reduced forms of molecular oxygen (e.g. superoxide radical, hydrogen peroxide and hydroxyl radical), known as reactive oxygen species (ROS), which are generated as normal metabolism byproducts, especially from respiration . These ROS are highly reactive molecules that are capable of damaging cellular constituents such as DNA, RNA, lipids and proteins . In adaptation to oxidative stress, aerobic organisms have evolved multiple enzymatic and non-enzymatic defense systems to protect their cellular constituents from ROS and to maintain their cellular redox state . Accumulation of ROS is known to increase under many, if not all, stress conditions as the defensive scavenging systems become insufficient to cope with increasing levels of stress.
The enzymatic scavenging system for ROS involves a number of enzyme-catalyzed reactions in different cellular compartments. A series of peroxidases referred to as peroxiredoxins (Prxs) that are ancestral thiol-dependent selenium- and heme-free peroxidases  have been found from archaea, lower prokaryotes to higher eukaryotes. These peroxidases constitute a large family including bacterial AhpC proteins and eukaryotic thioredoxin peroxidases (TPxs) . Prxs are abundant, well-distributed peroxidases that reduce H2O2, organic peroxides and peroxynitrite at the expense of thiol compounds. Thus, Prxs are considered alternative hydroperoxide scavenging enzymes, as they can reduce both organic and inorganic peroxides as well as oxidized enzymes. Based on the number of cysteine residues involved in catalysis, Prxs can be divided into three classes: typical 2-Cys Prxs, atypical 2-Cys prxs and 1-Cys Prxs . Prxs are ubiquitous proteins that use an active site Cys residue from one of the homodimers to reduce H2O2. The peroxidative cysteine sulfenic acid formed upon reaction with peroxide is reduced directly by glutathione. It is suggested that Prxs can act alternatively as peroxidases or as molecular chaperones by changing their molecular complexes. Furthermore, the oxidized cysteinly species, cysteine sulfenic acid, may play a dual role by acting as a catalytic intermediate in the peroxidase activity and as a redox sensor in regulating H2O2-mediated cell defense signaling.
Alkyl hydroperoxide reductase (Ahp) is the second known member of a class of disulfide oxidoreductases  and a member of the thiol-dependent peroxiredoxin family , which possesses activity against H2O2, organic peroxides, and peroxynitrite . Therefore, expression of Ahp genes plays an important role in peroxide resistance (oxidative stress) in Bacillus subtilis , Clostridium pasteurianum  and Burkholderia cenocepacia . Moreover, the compensatory expression of AhpC in Burkholderia pseduomallei katG is essential for its resistance to reactive nitrogen intermediates .
In this article, we report the isolation of DhAHP from the extreme halophilic yeast D. hansenii via subtractive hybridization of cDNA isolated from high salt treated vs. non-treated cells. Further characterization of DhAHP showed that it is a gene orthologous to alkyl hydroperoxide reductase of Candida albicans (Gene ID: 3637850 AHP11). On the basis of the deduced amino acid sequence, we propose that DhAhp be classified as an alkyl hydroperoxide reductase. Silencing of its expression in D. hansenii by RNAi resulted in decreased tolerance while overexpression conferred enhanced tolerance to salinity. Furthermore, overexpression of DhAHP in the salt-sensitive S. cerevisiae and P. methanolica also endowed upon their cells greater tolerance to NaCl. These overexpression transformants exhibited reduced levels of ROS under salinity stress. These results suggest that the cytosolic Ahp, induced and accumulated under saline conditions, may play a key role in this extremely halophilic yeast in adaption to high salinity by scavenging ROS, serving as chaperone and mediating H2O2-mediated defense signaling.
Characterization of salt-induced gene in D. hansenii
In this study, forward subtractive hybridization PCR was employed to investigate the genes of D. hansenii that are induced by salt. The subtracted cDNA library was enriched in differentially expressed sequences after treatment with 2.5 M NaCl for 24 min, relative to control cDNA. One of the selected clones that showed a significant increase in expression after salt induction is a homolog to the gene encoding for alkyl hydroperoxide reductase in C. albicans (Gene ID: 3637850 AHP11). This D. hansenii gene, DhAHP, was further characterized for its genomic organization, expression pattern and function.
Cloning of full-lengthed cDNA of DhAHP
Characteristics of DhAHPand related genes
Phylogenetic analysis revealed that the DhAhp protein is more homologous to yeast Ahps than to other Ahps from plants or peroxiredoxins from mammals. The DhAhp is located in the same subgroup as Ahps from yeasts, such as C. albicans and S. cerevisiae. Taken together, these results suggest that the Ahp of D. hansenii is more closely related to those of yeasts than to the plant Ahps or mammalian peroxiredoxins. It is conceivable that its function or enzymatic characteristics may be close to those of yeast Ahps (Fig. 3B).
Genome organization and expression of DhAHP
Silencing by RNA interference and overexpression of DhAHP in D. hansenii
Overexpression of DhAHP in S. cerevisiae and P. methanolica
Organisms are constantly exposed to various stresses, which cause considerable reduction in growth. In adaptation, organisms respond to stress through a number of physiological and developmental changes. Thus, expression of many genes is altered in such responses. Identification of the particular gene or genes responsible for the specific adaption to such stimuli is a major challenge in modern biology; it requires methods which rapidly and efficiently compare the transcripts expressed in the organism subject to stress. An equalizing cDNA subtraction hybridization method provides the technical basis for such a comparison. It has been demonstrated successfully to clone a number of differentially expressed genes . Isolation of differentially expressed genes in the extremely halophilic yeast D. hansenii would serve as an initial step towards understanding its tolerance mechanisms against salinity.
Salt-induced genes in D. hansenii
As discussed in the Background section, a number of salt-related genes have been identified in the extremely halophilic yeast D. hansenii. As expected, most of the salt-upregulated genes identified so far are involved in osmoregulation or transport of ions. By using forward subtractive hybridization, we have identified, cloned and sequenced DhAHP, a new salt induced gene, from D. hansenii by applying salt stress. Further characterization of the functional role of the gene will aid to our understanding of the underlying halotolerance mechanisms in this halophilic yeast.
Characterization of salt-induced DhAHPand its protein
High salinity, which is caused typically by NaCl, results in ion toxicity and hyperosmotic stress leading to numerous secondary pathological effects including generation of ROS  and programmed cell death. It's not surprising that one of the major upregulated genes under salinity stress, DhAHP, is orthologous to the alkyl hydroperoxide reductase of the peroxiredoxin family. Ahp is a member of the peroxiredoxin family of enzymes, which possess activity against H2O2, organic peroxides, and peroxynitrite . DhAHP has not been previously described for its role in salt tolerance in D. hansenii. Comparison of protein sequences showed that DhAhp shares a high similarity to Ahp11 of the yeast C. albicans. Multiple sequence alignment analysis of Ahps showed the protein from D. hansenii has a high similarity to that of C. albicans (Fig. 3A) and phylogenetic analysis revealed that Ahp of D. hansenii is more closely related to the yeast than to the plant or mammalian peroxiredoxins (Fig. 3B). Thus, DhAhp belongs to the alkyl hydroperoxide reductase of the peroxiredoxin family. Previously, Kurtzman and Robnett  have suggested that D. hansenii is phylogenetically related to C. albicans based on the fact that they are both ascomycetous yeasts. The high similarity between the Ahps from both species further supports this notion. In addition, both organisms use an alternative genetic yeast code in which the CUG codon may be used as a serine codon . Taken together, these results suggest that DhAhp and C. albicans Ahp11 have common ancestry, but show divergent evolution.
The closest structural homolog to DhAHP is the PrxD (Type Ii) of Populus tremula (PDB:1TP9A) (data not shown), which contains two cysteine residues. Though poplar Prx contains two conserved cysteine residues, it is assumed to function as a 1-Cys Prx because site-directed mutagenesis has demonstrated that only the catalytic cysteine of the poplar Prx is essential for hydroperoxide reduction . Previously, the type II TPx from S. cerevisiae was reported to contain three Cys residues at positions 31, 62 and 120, and its disulfide linkage is between 62 and 120 and Cys-31 has no effect on TPx activity . Though structural and sequence analyses of the deduced protein indicate that DhAhp contains 2 Cys residues at positions 24 and 54, the multiple sequence alignment of Ahps identifies the conserved Cys-54 as the peroxidative cysteine (Fig. 3). The role of Cys-24 in D. hansenii Ahp remains to be explored in the future. Therefore, DhAhp is clearly a member of the disulfide oxidoreductases and can be considered a 1-Cys Prx.
Regulation of expression of DhAHP
Alkyl hydroperoxide reductases have been identified previously as oxidative stress proteins in Salmonella typhimurium  and Bacillus subtilis  and their expression is known to be upregulated by oxidative factors. However, the finding of an extensive accumulation of Ahp in the halophilic yeast D. hansenii by salt is reported for the first time in this study. Consistently, overexpression of D. hansenii Ahp in D. hansenii (Fig. 7) and in the two salt-sensitive yeasts S. cerevisiae and P. methanolica (Fig. 8 and 9) further increases their tolerance to salt. On the contrary, suppression of its expression in D. hansenii resulted in a lower tolerance to salinity (Fig. 6). Clearly, the results suggest that DhAHP is induced by salt and its expression confers the high salt tolerance in D. hansenii. A previous study also revealed that the expression of a homolog to the Escherichia coli Ahp is induced by osmotic shock in Staphylococcus aureus . Similarly, the expression of Ahp in Shewanella putrefaciens is accompanied by accumulation of the corresponding transcript under NaCl stress  and the activity of the alkyl hydroperoxidase enzyme is dependent on salt concentration . Collectively, the results from these studies indicate that expression of Ahps in general is upregulated not only by oxidative factors but also by other stresses, such as drought and salinity.
Hydrogen peroxide level is known to increase within the cell in response to various stress factors and act as an intracellular messenger for induction of genes related to defense against oxidative environments . Treatment of cells with hydrogen peroxide mimics stress and induces defense signaling by activating mitogen-activated protein kinase and stimulates cell growth . The ROS levels of D. hansenii, S. cerevisiae and P. methanolica also increase in response to salt and methanol treatments, and the degrees of increase are more pronounced in the two salt-sensitive yeast species than the halophilic D. hansenii (Fig. 11). Furthermore, the DhAHP overexpression transformants of these species have reduced amounts of ROS accumulated than their wild type strains, indicating the protective role of Ahp. These results are in agreement with the earlier observations that Ahp genes play an important role in peroxide resistance in Bacillus subtilis , Clostridium pasteurianum , Burkholderia cenocepacia , Shewanella putrefaciens  and Porphyromonas gingivalis  under various stress conditions (e.g. hydrogen peroxide, high/low temperature and high/low pH). Therefore, the induced expression and accumulation of DhAhp in saline environments to detoxify ROS is a very important survival mechanism for this halophilic organism.
In summary, the Ahp gene isolated from the extremely halophilic yeast D. hansenii under salt stress in this study is a new gene relative to its salt tolerance mechanism. It is rapidly induced and accumulates to large quantities in D. hansenii to reduce accumulation of ROS. Molecular characterization shows that DhAhp, a cytosolic protein, belongs to the alkyl hydroperoxide reductase of the 1-Cys type peroxiredoxin family. The DhAhp and C. albicans Ahp11 have a common ancestry but show divergent evolution. Silencing of its expression by RNA interference resulted in decreased tolerance to salt stress. On the other hand, overexpression of the DhAHP in D. hansenii and the two salt-sensitive yeasts S. cerevisiae and P. methanolica conferred enhanced tolerance to salt with reduced accumulation of ROS. Clearly, the multiple activities (peroxidase, chaperone, redox signaling) possessed by Ahps are essential for its central role in protecting the cellular metabolism of yeast against ROS built-up under stress conditions. Compared with the two salt-sensitive yeasts, the extreme halotolerance exhibited by D. hansenii may be due to its ability to scavenge ROS by Ahp. Thus, the results of this study contribute to our understanding of the underlying mechanisms by which the extremely halophilic yeast D. hansenii adapts to high salt. Manipulation of antioxidant enzymes in industrial microorganisms, as demonstrated in S. cerevisiae and P. methanolica in this study, or crops may bring about enhanced growth and production of useful products under adverse culture conditions. Overexpressing enzymes involved in redox reaction in crops, such as superoxide dismutase  and glutathione peroxidase  has resulted in enhanced tolerance to salt and other stress.
Yeast strains and growth conditions
The yeast strains used in this work included D. hansenii strain BCRC No. 21947, isolated from Hsilo County, Taiwan, S. cerevisiae Neo Type strain Y1 BCRC No. 21447 from brewer's top yeast, obtained from FIRDI (Food Industry Research and Development Institute, Hsin-chu City, Taiwan), and P. methanolica strain PMAD11 genotype ade2-11, obtained from Invitrogen, U.S.A. D. hansenii was cultured at 24°C in YM medium (0.3% yeast extract, 0.3% malt extract, 0.5% peptone, 1% dextrose) while S. cerevisiae and P. methanolica were cultured at 28°C in YPD medium (1% yeast extract, 2% peptone, 2% dextrose) and YPAD medium (1% yeast extract, 2% peptone, 2% dextrose, 0.01% adenine), respectively.
RNA extraction and poly(A+) RNA purification
Total RNA was extracted with a modified hot phenol protocol . Poly (A+) RNA was isolated from total RNA using Mag-Net mRNA Isolation Kit according to the manufacturer's instruction (Amresco, Inc. USA). Concentration of RNA was determined using a NanoDrop spectrophotometer (NanoDrop, Wilmington, USA). RNA quality was verified by electrophoresis on 1.5% formaldehyde agarose gel and stained with ethidium bromide.
Subtractive hybridization and construction of subtracted cDNA library
Subtractive hybridization was performed using PCR-select cDNA Subtraction Kit (Clontech, Palo Alto, CA, U.S.A.). For screening of differentially upregulated genes, cDNA synthesized from the 2.5 M NaCl treated yeast cells for 24 min was used as the tester while that from non-treated cells served as the driver. The PCR products of forward subtraction were subcloned into the pGEMR-T Easy Vector (Promega, USA). Competent cells of E. coli (XL-Blue) was transfected with the plasmids and grown on LB-agar medium containing 5-bromo-4-chloro-3-indolyl-b-d-galactoside (X-gal) (Sigma, U.S.A.), isopropyl β-D-1-thiogalactopyranoside (IPTG) (Sigma, U.S.A.) and ampicillin. Individual white colonies with insert DNA were randomly picked for further analysis.
Sequencing and sequence analysis
White clones from the forward subtractive hybridization libraries were sequenced with the universal T7 or SP6 sequencing primers using an automatic DNA sequencer (3100 Genetic Analyzer, ABI, U.S.A). All inserted sequences were queried for similarity through the NCBI database using BLASTX sequence comparison software http://0-www.ncbi.nlm.nih.gov.brum.beds.ac.uk/BLAST.
Quantification of DhAHPby quantitative real-time PCR (Q-RT-PCR)
Total RNA isolated from yeast cells treated with NaCl for various time intervals was first treated with DNase I (Promega, U.S.A.) to remove DNA contamination before cDNA synthesis . cDNA was synthesized using High Capacity cDNA Reverse Transcription Kit (P/N 4368814, ABI, U.S.A.) for RT-PCR according to the manufacturer's instruction. The sequence forward and reverse primers for Q-RT-PCR were designed using the primer ExpressR Software provided by Applied Biosystems. A set of D. hansenii 18S ribosomal RNA primers was designed for use as an endogenous control.
18S forward: G'-CGTCCCTGCCCTTTGTACAC-3'
18S reverse: G5'-GCCTCACTAAGCCATTCAATCG-3'
DhAHP target forward: G5'-GGAGCCCCAGGAGCATTTA-3'
DhAHP target reverse: G5'-TGGGCCAAATAATCGGGAAT-3'
Real-time PCR assay was carried out in an ABI PRISM 7500 Sequence Detection System (ABI, U.S.A.). The amplification of the target genes was monitored every cycle by SYBR-Green fluorescence.
Rapid amplification of cDNA ends (RACE)
The full-lengthed cDNA clone of DhAHP was obtained by rapid amplification of the cDNA ends using the GeneRacerTM Kit (Invitrogen, U.S.A.), as described in the manual provided by the manufacturer. The forward and reverse gene specific primers (GSPs) used for RACE were designed based on the DhAHP cDNA sequence. The universal primers for 5' and 3' Race were GeneRace 5' and GeneRace 3', respectively, provided in the kit. After PCR the DNA fragments were cloned into pGEMR-T Easy vector (Promega, U.S.A.) for sequencing.
Forward (GSP): 5'- GTCAATGCTGCTTGGGGTAAAGCTTTA-3'
Reverse (GSP):5'- GGTCTCAGCACTGGAAATTTCAGTG-3'
GeneRace 5':5'- CGACTGGAGCACGAGGACACTGA-3'
GeneRace 3':5'- GCTGTCAACGATACGCTACGTAACG-3'
The deduced amino acid sequence of DhAHP was analyzed with the Expert Protein Analysis System http://www.expasy.org/. Multiple sequence alignment was performed for sequence comparison and alignment of D. hansenii Ahp and two other reported AHPs (Swiss-Prot: P38013 and Q5AF44) from S. cerevisiae and C. albicans and peroxisomal membrane protein (Swiss-Prot: O14313) from S. pombe and three other structural homolog proteins (Swiss-Prot:Q8S3L0, B3GV28 and P30044) from P. tremula, P. sativum and H. sapiens. The alignment and phylogenetic analysis were carried out by the protein sequence alignment program CLUSTAL W.
Southern and northern hybridization analysis
Genomic DNA was isolated from yeast cells by the method of Hoffman and Winston . Southern and northern hybridization analyses were performed using the DIG High Prime DNA Labeling and Detection Starter Kit (Roche Diagnostics, Switzerland). For Southern hybridization, 20 μg genomic DNA was digested with EcoRI and BamHI and electrophoretically separated on 0.7% (w/v) agarose gels in TBE buffer and DNA fragments blotted onto nylon membrane (Amersham Pharmacia Biotech, U.K.) by 20×SSC. The full-lengthed DhAHP DNA was labeled and used as a hybridization probe. For nothern hybridization analysis, RNA was extracted from D. hansenii that was not treated or treated with 2.5 M NaCl for 16 min, separated by electrophoresis in formaldehyde gels, blotted onto nylon membrane and hybridized with labeled DhAHP DNA, as described above for Southern analysis.
Silencing of DhAHP expression in D. hanseniiby RNA interference
To test the function of DhAHP, RNA interference was employed to suppress its expression in D. hansenii using the Knockout RNAi System Kit (Clontech, U.S.A.), as described in the manual by the manufacturer. The oligonucleotide sequences including BamHI and EcoRI sites, target sense sequence, hairpin loop, target antisense sequence and terminator were shown as follow.
BamHI Target sense sequence Hairpin loop Target antisense sequence Terminator
A chemical method based on LiCl, as described by Tarutina and Tolstorukov , was used to transfect D. hansenii and the RNAi transformant was screened by its poor ability to grow on YM11 solid media containing 2.5 M NaCl. The transformant was confirmed by sequencing the introduced DNA fragment in the genome with specific primers and by Q-RT-PCR.
Overexpression of DhAHP in D. hansenii, S. cerevisiae and P. methanolica
To further test its functional role in relation to salt tolerance, DhAHP was overexpressed in three yeast species with contrasting degrees of salt tolerance. The entire ORF of DhAHP was first amplified by PCR utilizing the overexpression 5' primer, which introduced an EcoRI site in front of the starting ATG codon, and the overepression 3' primer, which introduced a BamHI site before the stop codon. This DNA fragment was inserted into the expression vector of pMETB (Invitrogen, U.S.A.). The plasmid DNA of the DhAHP/pMETB veector was digested with Pst I to release the P AUG1 /DhAHP expression cassette, which was then introduced into D. hansenii, S. cerevisiae and P. methanolica by a chemical method based on LiCl, as described by Tarutina and Tolstorukov . The AUG1 sequence is a methanol inducible promoter to drive the expression of introduced DhAHP. Functional complementation was used to screen transformants from the three species by culture on solid media containing 0.5% methanol and higher NaCl concentrations than they can normally tolerate. For isolation of D. hansenii overexpression transformants YM medium containing 3.5 M NaCl was used, for S. cerevisiae transformants YPD medium containing 1.5 M NaCl was used and for P. methanolica transformants YPAD medium containing 2.0 M NaCl was adopted. The transformants were confirmed by sequencing the P AUG1 DNA fragment in the genome with specific primers and by Q-RT-PCR with cells grown under high salt in the presence or absence of methanol. The ability of the selected transformants to tolerate salt was further assessed by growing in liquid media containing high NaCl concentrations.
Measurement of intracellular ROS
For measurement of cellular ROS, the redox-sensitive fluorescent probe 2', 7'-dihydrodichlorofluorescein diacetate (DCFA-DA) (Sigma, U.S.A.) was used according to Chattopadhyay et al. . The cells of wild type strains and DhAHP overexpression transformants were grown in appropriate liquid media without any salt for approximately 36 h (1 O.D. at 600 nm) and switched to fresh media containing high NaCl (3.5 M for D. hansenii, 2.0 M for S. cerevisiae and 2.5 M for P. methanolica) with or without methanol for 5 h. To determine ROS, cells were harvested by centrifugation and treated with 10 μM DCFA for 30 min at 30°C. The cells were re-suspended and washed in water and extracted by vortexing with glass beads. Extracts were centrifuged and fluorescence in the supernatant was measured with λEX = 485 nm and λEM = 524 nm in a fluorescence spectrophotometer (Infinite F200). Fluorescence signals were expressed relative to that of the wild type strain before any stress treatments (fold over control).
The authors acknowledge the supports of Tainan District Agricultural Improvement Station, Council of Agriculture, Taiwan Executive Yuan and the Graduate Institute of Agricultural Biotechnology, National Chiayi University. The authors also thank Emery M. Ku for critical reading of the manuscript.
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