Exploration of Salt Adaptation Mechanisms in Desulfovibrio vulgaris Hildenborough

1. Exploration of Salt Adaptation Mechanisms in Desulfovibrio vulgaris Hildenborough Email:zhili.he@ou.edu Phone: 405-325-3958 Web site: http://ieg.ou.edu/ K138 Zhili He1,2,7, Qiang He2,3,7, Eric J. Alm4,7, Judy D. Wall5,7, Matthew W. Fields6,7, Terry C. Hazen4,7, Adam P. Arkin4,7, and Jizhong Zhou1,2,7 Abstract 1University of Oklahoma, Norman, OK 2Oak Ridge National Laboratory, Oak Ridge, TN. 3Temple University, Philadelphia, PA. 4Lawrence Berkeley National Laboratory, Berkeley, CA. 5University of Missouri, Columbia, MO. 6Miami University, Oxford, OH 7Virtual Institute for Microbial Stress and Survival, Berkeley, CA Fig. 4 Fig. 5 Salt adaptation mechanisms were explored in Desulfovibriovulgaris Hildenborough combining a global transcriptional analysis and physiological studies. D. vulgaris is a δ-Proteobacterium, a model sulfate-reducing bacterium, and well known for its metabolic versatility and wide distribution. D. vulgaris cells grew slower with a longer lag and generated reduced biomass at 250 or 500 mM NaCl, and did not grow at 1 M NaCl although growth was not significantly affected below 50 and 100 mM NaCl conditions. Comparison of D. vulgaris grown with and without yeast extract in the presence of 500 mM NaCl showed that D. vulgaris growth was inhibited ~ 35% with yeast extract, and that its growth was inhibited ~ 80% without yeast extract. Transcriptomic data revealed that predicted genes for leucine biosynthesis, heat-shock proteins, formate dehydrogenases, sensory box histidine kinases/response regulators, and peptidases were highly up-expressed in NaCl-adapted cells, and that predicted genes involved in tryptophan biosynthesis, ribosomal protein synthesis, energy metabolism, iron transport, and phage-related proteins were down-expressed. However, genes involved in glycine/betaine/L-proline ABC transport, Na+/H+ transport, K+ uptake and transport, proline biosynthesis and transport, and glycerol biosynthesis and transport were not significantly changed. This was different from our previous observations for salt shock in D. vulgaris. External addition of leucine or/and tryptophan into the LS medium without yeast extract significantly relieved the inhibitation of D. vulgaris growth under 500 mM NaCl conditions, which was consistent with the microarray data since the genes involved in tryptophan biosynthesis are strongly regulated by feedback mechanisms. An addition of other amino acids (e.g. glutamate and serine), precursors of tryptophan, or products of tryptophan could not relieve inhibition. The results suggested that the accumulation of metabolites (e.g. leucine and tryptophan) and nutrients may increase the adaptability of D. vulgaris to high salt conditions. Further studies will focus on the analysis of metabolites and on the elucidation of salt adaptation mechanisms in Desulfovibrio vulgaris Hildenborough. Gene expression of D. vulgaris related to operons for salt adaptation Fig. 2 Operon structure pssA leuA leuC leuD DVU2984 leuB DVU2809 DVU2810 DVU2811 fdnG-3 hspC DVU2442 • With yeast extract, D. vulgaris growth was inhibited ~ 35% by 500 mM NaCl, and its growth was inhibited ~ 80% by 500 mM NaCl without yeast extract (Fig. 4). • The results suggest that yeast extract significantly affects the growth of D. vulgaris in the presence of NaCl, which may be because certain substances in yeast extract help D. vulgaris cells adapt to high salinity environments. • Leu, Trp and Leu+Trp significantly relieved the inhibition of D. vulgaris grown at the LS medium without yeast extract and with 500 mM NaCl (Fig. 5), and other amino acids, products or precursors of Trp did not relieve such an inhibition (not shown). • The results are consistent with mciroarray data, and suggest that tryptophan and leucine may play important roles in D. vulgaris adaptation to salt stress. pspC pspF DVU2987 pspA leuB DVU0462 trpF-1 DVU0460 DVU0464 trpD DVU0461 aroA trpE trpG trpC trpB-2 trpA DVU2387 tolQ-1 DVU2385 oppC DVU2384 DVU2383 DVU2382 feoA feoB DVU2573 feoA pleD More confidence may be expected to incorporate operons or pathways for gene expression analysis. Comparison of expression levels of function-known genes under salt adaptation and salt shock Summary Materials and Methods • Genes for leucine biosynthesis, heat-shock proteins, formate dehydrogenases, sensory box histidine kinases/response regulators, and peptidases were highly up-expressed in NaCl-adapted cells. • Predicted genes involved in tryptophan biosynthesis, ribosomal protein synthesis, energy metabolism, and iron transport were down-expressed. • Genes involved in glycine/betaine/L-proline ABC transport, Na+/H+ transport, K+ uptake and transport, and proline biosynthesis and transport were not significantly changed. • Yeast extract, leu, Trp, or/and Leu+Trp significantly relieved the inhibition of D. vulgaris grown under 500 mM NaCl conditions, which suggests that an accumulation of metabolites (e.g. leucine and tryptophan) and availability of nutrients may increase the adaptability of D. vulgaris to high salt conditions. • Microarray data are consistent with RT-PCR results and physiological studies. • Future studies will focus on the analysis of metabolites accumulated in the cell. Cell culture and treatment:D. vulgaris cells were grown at the LS medium with or without yeast extract. To test the effects of amino acids on D. vulgaris growth, yeast extract was removed. NaCl was added into the LS medium to make desired concentrations when the LS medium was made. D. vulgaris oligonucleotidearray:70mer oligonucleotide arrays that containing all ORFs were constructed as described (He et al., in press). Target preparation, labeling and array hybridization:Total cellular RNA was isolated and purified using TRIzolTM Reagent, and then labeled with Cy5 dye. Genomic DNA was isolated and purified from D. vulgaris as described previously (Zhou et al., 1996), and then labeled with Cy3 dye. The labeled RNA and genomic DNA were co-hybridized to the array at 45oC with 50% formamide for 16 hrs in the dark. Image and data analysis were the same as described previously (Chhabra et al., 2006; Mukhopadhyay et al., in press). • Salt adaptation:D. vulgaris cells were grown in the LS medium containing 500 mM NaCl (added before inoculation). Samples were taken at OD ~= 0.40 for microarray hybridization. • Salt shock:D. vulgaris cells were grown in the LS medium to the mid-log (OD ~= 0.40), and NaCl was added to the culture. Samples were taken for microarray hybridization after 30-min NaCl (250 mM) treatment. • Differences and similarities in gene expression were seen between salt adaptation and salt shock (Table 3). Results References Cell growth at the LS medium containing different concentrations of NaCl 1. Chhabra SR, He Q, Huang KH, Gaucher SP, Alm EJ, He Z, Hadi MZ, Hazen TC, Wall JD, Zhou, J, Arkin AP and Singh AK (2006). J. Bacteriol.188: 1817-1828. 2. He Q, Huang KH, He Z, Alm EJ, Fields MW, Hazen TC, Arkin AP, Wall JD, and Zhou J. Appl. Environ. Microbiol.(in press). 3. Mukhopadhyay A, He Z, Yen HC, Alm EJ, He Q, Huang K, Baidoo EE, Chen W, Borglin SC, Redding A, Holman HY, Sun J, Joyner DC, Keller M, Zhou J, Arkin AP, Hazen TC, Wall JD, and Keasling JD. J. Bacteriol. (in press). 4. Zhou J, Bruns MA, and Tiedje JM (1996). Appl. Environ. Microbiol.62:461-468. • 50 and 100 mM NaCl did not affect the cell growth, and cells reached the stationary stage approximately 28 h after inoculation. • The cell growth was inhibited by 250 and 500 mM NaCl in two ways: the growth rate and the final biomass (measured by OD). • D. vulgaris could not grow in the LS medium in presence of 1 M NaCl. • 100, 250 and 500 mM were chosen for further experiments. Fig. 1 RT-PCR verification of microarray data Fig. 3 • 12 genes expressed in different levels were chosen for real-time PCR. • The correlation between microarray data and RT-PCR results were very good with r2 = 0.96 (n = 12). Acknowledgements This research was funded by the U.S. Department of Energy (Office of Biological and Environmental Research, Office of Science) grants from the Genomes To Life Program.