chemolithotrophic bacteria slideshare

33 650651, Kawasumi, T., Igarashi, U., Kodama, T., Minoda, Y. 0000002800 00000 n Oxidation of inorganic nitrogen compounds. In: Gould, G. W., Corry, J. E. L. 0000006065 00000 n These bacteria are common in the runoff from coal mines. To save content items to your account, Entropy Applied and Environmental Microbiology 32:567571. Autotrophy: Concepts of lithotrophic bacteria and their organic metabolism. Thiobacillus ferrooxidans: A study of some of the factors governing the growth and physiology of continuous and batch cultures on ferrous iron. [1] These molecules can be organic (chemoorganotrophs) or inorganic (chemolithotrophs). Baas Becking, L. G. M., Parks, G. S. 1927. 2023 Springer Nature Switzerland AG. ?C~9}*l,82,bbfYvAjLM.P01;!3h3$oal|`fL%o3&00|``~)QAFF/$b`4 Microbiol. Find out more about the Kindle Personal Document Service. 17 491493, Burggraf, S., Olse, G. J., Stetter, K. O., Woese, C. R. 1992 A phylogenetic analysis of Aquifex pyrophilus Syst. Microbiol. . on the Manage Your Content and Devices page of your Amazon account. Even after decades of studies on sulfur oxidation by these bacteria, this problem has not been fully resolved although it is widely thought . 129 221226, Beudeker, R. F., de Boer, W., Kuenen, J. G. 1981bHeterolactic fermentation of intracellular polyglucose by the obligate chemolithotroph Thiobacillus neapolitanus under anaerobic conditions FEMS Microbiol. Microbiologist at Maharshi Dayanand University. Epub 2017 Jan 4. How do free living nitrogen fixers and plant associated nitrogen fixers differ? 14. Ecol. Journal of Bacteriology 110:633642. That is, they derive their energy from the energy already stored in chemical compounds. Microbiol. 12 337342, Bock, E. 1976 Growth of Nitrobacter in the presence of organic matter. Some microbes are chemolithoheterotrophs, using an inorganic chemical for their energy and electron needs, but relying on organic chemicals in the environment for their carbon needs. Winogradsky, S. 1887. nov., a marine obligately chemolithotrophic hydrogen-oxidizing bacterium Int. Most chemoautotrophs are extremophiles, bacteria or archaea that live in hostile environments (such as deep sea vents) and are the primary producers in such ecosystems. 151 252256, Horowitz, N. H. 1945 On the evolution of biochemical synteses Proc. The Calvin cycle is the most common CO2 fixation mechanism, and the reductive TCA cycle, acetyl-CoA pathway and 3-hydroxypropionate cycle are found in some chemolithotrophic prokaryotes. 0000082072 00000 n Winogradsky, S., 1888. endstream endobj 2324 0 obj <>/Filter/FlateDecode/Index[103 2161]/Length 66/Size 2264/Type/XRef/W[1 1 1]>>stream Colorless sulfur bacteria oxidize hydrogen sulfide (H2S) by accepting an electron from the compound. 76 252264, van Niel, C. B. 2. . Chemolithotrophy. Content may require purchase if you do not have access. 114 113, Kelly, D. P. 1981 Introduction to the chemolithotrophic bacteria M. P. Starr, H. Stolp, H. G. Trper, A. Balows, and H. G. Schlegel (ed.) Pan Y, Kang P, Tan M, Hu J, Zhang Y, Zhang J, Song N, Li X. "Chemoautotrophic and Chemolithotrophic Bacteria Trans. A., Brierley, C. L. 1968 Urea as a nitrogen source of thiobacilli J. Bacteriol. Evol. Epub 2016 Aug 5. 46 329337, London, J., Rittenberg, S. C. 1967 Thiobacillus perometabolis nov. Encyclopedia of Earth Sciences Series. Abt. FOIA Electrons from these electron donors are transferred to coenzyme Q or to cytochromes. Chemoautotrophic bacteria and chemolithotrophic bacteria obtain their energy from the oxidation of inorganic (non-carbon) compounds. Serol. Electron micrographs of GISH for OTU0001 on a mineral-enriched biochar particle. Energetic aspects of the metabolism of reduced sulphur compounds in Thiobacillus denitrificans. Suzuki, I. Soc. 338 400406, Kondratieva, E. N. 1989 Chemolithotrophy of phototrophic bacteria H. G. Schlegel and B. Bowien (ed.) Badziong, W., Thauer, R. K., Zeikus, J. G. 1978. General Microbiology by Linda Bruslind is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License, except where otherwise noted. Its role in the metabolism of some chemolithotrophs is probably very ancient. Journal of Bacteriology 134:718727. and Eikelboom type 021 N bacteria) isolated from wastewater-treatment plants and description of Thiothrix eikelboomii sp. References Natl. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. https://doi.org/10.1007/978-1-4020-9212-1_53, Shipping restrictions may apply, check to see if you are impacted, Reference Module Physical and Materials Science, Tax calculation will be finalised during checkout. 478503, Kelly, D. P., Smith, N. A. However, the date of retrieval is often important. Chemoautotrophs generally fall into several groups: methanogens, sulfur oxidizers and reducers, nitrifiers, anammox bacteria, and thermoacidophiles. Aleem, M. I. H. 1970. Springer, New York, NY. The chemotroph designation is in contrast to phototrophs, which use photons. 153 105110, Brierley, J. Trudinger, P. A. Biochar and mineral-enriched biochar (MEB) have been used as soil amendments to improve soil fertility, sequester carbon and mitigate greenhouse gas emissions. J Environ Manage. 0000015112 00000 n For clarity, only the immediate neighborhood of the OTU0001s clade is shown. Chemoautotrophs can use inorganic energy sources such as hydrogen sulfide, elemental sulfur, ferrous iron, molecular hydrogen, and ammonia or organic sources to produce energy. Abstract. 151 232237, Kristjansson, J. K., Ingason, A., Alfredsson, G. A. official website and that any information you provide is encrypted 2. 52 452484, Wachtershauser, G. 1990a The case for the chemo-autotrophic origin of life in an iron-sulfur world Origins of Life and Evolution of the Biosphere 20 173176, Wachtershauser, G. 1990b Evolution of the first metabolic cycles Proc. Kelly, D. P., Wood, A. P., Gottschal, J. C., Kuenen, J. G. 1979. Aromatic-turmerone ameliorates DSS-induced ulcerative colitis via modulating gut microbiota in mice. Free access to premium services like Tuneln, Mubi and more. Microbiol. Part of Springer Nature. A., de Bruijn, P., Robertson, L. A., Jetten, M. S. M., Kuenen, J. G. 1997 Metabolic pathway of anaerobic ammonium oxidation on the basis of 15N studies in a fluidized bed reactor Microbiology (UK) 143 24152421, van Gool, A., Tobback, P. P., Fischer, I. 2, part I 960, Schmidt, I., Bock, E. 1997 Anaerobic ammonia oxidation with nitrogen dioxide by Nitrosomonas eutropha Arch. . 57 121, Woese, C. R. 1987 Bacterial evolution Microbiol. Bacteriol. Google Scholar. eCollection 2022. The roles of exogenous organic matter in the physiology of chemolithotrophic bacteria. 0000009714 00000 n ( a ) Non-metric multidimensional scaling plot illustrating the similarities between individual samples, Phylogenetic tree based on the OTU0001s partial 16S rRNA gene sequence (482 nucleotides), Metabolic reconstructions of the three dominant bacteria (that is, Gama1, Oxal1 and Thio1), Electron micrographs of GISH for OTU0001 on a mineral-enriched biochar particle. Upper Saddle River, NJ: Prentice Hall. please confirm that you agree to abide by our usage policies. ber Schwefelbacterien. A chemotroph is an organism that obtains energy by the oxidation of electron donors in their environments. Autotrophic bacteria Springer-Verlag Berlin and Science Tech Publishers Madison WI 1732, Zillig, W., Yeats, S., Holz, I., Bck, A., Gropp, F., Rettenberger, M., Lutz, S. 1985 Plasmid-related anaerobic autotrophy of the novel archaebacterium Sulfolobus ambivalens Nature 313 789791, Zillig, W., Yeats, S., Holz, I., Bck, A., Rettenberger, M., Gropp, F., Simon, G. 1986 Desulfurolobus ambivalens gen. nov., sp. Later, the term would include also the chemoorganoautotrophy, that is, it can be seen as a synonym of chemoautotrophy.[4][5]. 153 294298, Nishihara, H., Igarashi, Y., Kodama, T. 1991 Hydrogenovibrio marinus gen. nov. sp. Kelly, D. P. 1967. Moreover, there is no sunlight. 0000016332 00000 n 1976 Ferric iron reduction by sulfur-and iron-oxidizing bacteria Appl. 15. Chemoautotrophic and Chemolithotrophic Bacteria The metabolism of inorganic sulphur compounds by thiobacilli. Canadian Journal of Microbiology 23:319324. Trends Ecol. By accepting, you agree to the updated privacy policy. Gen. Microbiol 27 121149, Winogradsky, S. 1887 ber Schwefelbacterien Bot. 45 489600, 606616, Winogradsky, S. 1922 Eisenbakterien als Anorgoxydanten Centralbl. @free.kindle.com emails are free but can only be saved to your device when it is connected to wi-fi. 146 382389, Zavarzin, G. A. Department of Geological and Environmental Sciences, Stanford University, Stanford, California 94305-2115 of your Kindle email address below. 42 483492, Umbreit, W. W. 1947 Problems of autotrophy Bact. P., Monosov, E. Z. (February 22, 2023). What conversion is occurring for each? Two types of anaerobic chemolithotrophs oxidize hydrogen with carbon dioxide as electron acceptor: methanogens and homoacetogens, producing methane and acetate, respectively. The presence of chemolithotrophic sulfur-oxidizing bacteria in the sulfide-containing hydrothermal water supports the hypothesis that chemosynthesis provides a substantial primary food source for the rich populations of invertebrates found in the immediate vicinity of the vents. 2022 Jun 22;13:895975. doi: 10.3389/fmicb.2022.895975. Bookshelf Chemoorganotrophic growth of Nitrobacter agilis Arch. Google Scholar. 211240. 0000043160 00000 n Proceedings of the National Academy of Sciences of the United States of America 54:869873. Because each style has its own formatting nuances that evolve over time and not all information is available for every reference entry or article, Encyclopedia.com cannot guarantee each citation it generates. Weve updated our privacy policy so that we are compliant with changing global privacy regulations and to provide you with insight into the limited ways in which we use your data. Microbiol. Autotrophic bacteria Springer-Verlag, Berlin and Science Tech Publishers Madison WI 115, Brock, T. D., Gustafson, J. 1993 Hydrogenobacter acidophilus sp. nov., a novel hyperthermophilic archaeum that oxidizes Fe2 + at neutral pH under anoxic conditions, The chemolithotrophic bacterium Thiobacillus ferrooxidans, Reasons why Leptospirillum-like species rather than Thiobacillus ferrooxidans are the dominant iron-oxidizing bacteria in many commercial processes for the biooxidation of pyrite and related ores, A new chemolithoautotrophic arsenite-oxidizing bacterium isolated from a gold mine: phylogenetic, physiological, and preliminary biochemical studies, Response of Thiobacillus ferrooxidans to phosphate limitation, Enumeration and detection of anaerobic ferrous iron-oxidizing, nitrate-reducing bacteria from diverse European sediments, Anaerobic, nitrate-dependent microbial oxidation of ferrous iron, Molybdenum oxidation by Thiobacillus ferrooxidans, Molecular aspects of the electron transfer system which participates in the oxidation of ferrous ion by Thiobacillus ferrooxidans, Characterization and thermostability of a membrane-bound hydrogenase from a thermophilic hydrogen oxidizing bacterium, Bacillus schlegelii, Bioscience, Biotechnology and Biochemistry, Crystal structure and mechanism of CO dehydrogenase, a molybdo iron-sulfur flavoprotein containing S-selanylcysteine, Proceedings of the National Academy of Sciences, USA, Genetic analysis of Carboxydothermus hydrogenoformans carbon monoxide dehydrogenase genes cooF and cooS, Binding of flavin adenine dinucleotide to molybdenum-containing carbon monoxide dehydrogenase from Oligotropha carboxidovorans: structural and functional analysis of a carbon monoxide dehydrogenase species in which the native flavoprotein has been replaced by its recombinant counterpart produced in Escherichia coli, Genes encoding the NAD-reducing hydrogenase of Rhodococcus opacus MR11, Location, catalytic activity, and subunit composition of NAD-reducing hydrogenases of some Alcaligenes strains and Rhodococcus opacus MR22, Effect of molybdate and tungstate on the biosynthesis of CO dehydrogenase and the molybdopterin cytosine-dinucleotide-type of molybdenum cofactor in Hydrogenophaga pseudoflava, Phylogenetic position of an obligately chemoautotrophic, marine hydrogen-oxidizing bacterium, Hydrogenovibrio marinus, on the basis of 16S rRNA gene sequences and two form I RuBisCO gene sequences, Characterization of hydrogenase activities associated with the molybdenum CO dehydrogenase from Oligotropha carboxidovorans, Nitrate respiratory metabolism in an obligately autotrophic hydrogen-oxidizing bacterium, Hydrogenobacter thermophilus TK-6, Redox state and activity of molybdopterin cytosine dinucleotide (MCD) of CO dehydrogenase from Hydrogenophaga pseudoflava, The genes for anabolic 2-oxoglutarate:ferredoxin oxidoreductase from Hydrogenobacter thermophilus TK-6, Biochemical and Biophysical Research Communications, Oxidation of molecular hydrogen and carbon monoxide by facultatively chemolithotrophic vanadate-reducing bacteria, Whole-genome transcriptional analysis of chemolithoautotrophic thiosulfate oxidation by Thiobacillus denitrificans under aerobic versus denitrifying conditions, Carbon metabolism of filamentous anoxygenic phototrophic bacteria of the family Oscillochloridaceae, Organization of carboxysome genes in the thiobacilli, Retrobiosynthetic analysis of carbon fixation in the photosynthetic eubacterium Chloroflexus aurantiacus, Modified pathway to synthesize ribulose 1,5-bisphosphate in methanogenic Archaea, Properties of succinyl-coenzyme A:D-citramalate coenzyme A transferase and its role in the autotrophic 3-hydroxypropionate cycle of Chloroflexus aurantiacus, Properties of succinyl-coenzyme A:L-malate coenzyme A transferase and its role in the autotrophic 3-hydroxypropionate cycle of Chloroflexus aurantiacus, The molecular regulation of the reductive pentose phosphate pathway in Proteobacteria and cyanobacteria, Deduced amino acid sequence, functional expression, and unique enzymatic properties of the form I and form II ribulose bisphosphate carboxylase oxygenase from the chemoautotrophic bacterium Thiobacillus denitrificans, A bicyclic autotrophic CO2 fixation pathway in Chloroflexus aurantiacus, Autotrophic CO2 fixation pathways in archaea (Crenarchaeota), Evidence for autotrophic CO2 fixation via the reductive tricarboxylic acid cycle by members of the -subdivision of Proteobacteria, Autotrophic carbon dioxide fixation in Acidianus brierleyi, Occurrence, biochemistry and possible biotechnological application of the 3-hydroxypropionate cycle, Evidence for the presence of the reductive pentose phosphate cycle in a filamentous anoxygenic photosynthetic bacterium, Oscillochloris trichoides strain DG-6, Induction of carbon monoxide dehydrogenase to facilitate redox balancing in a ribulose bisphosphate carboxylase/oxygenase-deficient mutant strain of Rhodospirillum rubrum, Carbon metabolism in Eubacterium limosum: a C-13 NMR study, The role of an iron-sulfur cluster in an enzymatic methylation reaction: methylation of CO dehydrogenase/acetyl-CoA synthase by the methylated corrinoid iron-sulfur protein, A global signal transduction system regulates aerobic and anaerobic CO2 fixation in Rhodobacter sphaeroides, The reductive acetyl coenzyme A pathway. This is a preview of subscription content, access via your institution. A., Denend, A. R. 1972 Ribulose diphosphate carboxylase from autotrophic microorganisms J. Bacteriol. dkNET Office Hours - "Are You Ready for 2023: New NIH Data Management and Sha REGENERATIVE BRAKING IN ELECTRIC VEHICLES.pptx, Easy-handling carbon nanotubes decorated poly(arylene ether nitrile).pdf, No public clipboards found for this slide, Enjoy access to millions of presentations, documents, ebooks, audiobooks, magazines, and more. Coupled Photochemical and Enzymatic Mn(II) Oxidation Pathways of a Planktonic Roseobacter-Like Bacterium Biotechnol. The chemolithotrophic bacteria and archaea are defined by their ability to oxidize inorganic atoms or molecules as a growth-supporting reductant and energy source. Chemotrophs can be found in areas where electron donors are present in high concentration, for instance around hydrothermal vents. These nitrifying bacteria are important in the operation of the global nitrogen cycle. Microbiol. The site is secure. 0000015669 00000 n A lithoautotroph is an organism which derives energy from reactions of reduced compounds of mineral (inorganic) origin. Pune-4, Biochemistry: A Brief History of Biochemsitry, A Pragmatic Approach for Solving the Sports Scheduling Problem-presentation.pdf. ber Schwefelbacterien. 0000004006 00000 n 147 184189, Barros, M. E. C., Rawlings, D. E., Woods, D. R. 1984 Mixotrophic growth of a Thiobacillus ferrooxidans strain Appl. Now customize the name of a clipboard to store your clips. Microbiol. Origins of Life 8:173174. Activate your 30 day free trialto continue reading. 5 291299, Brierley, C. L., Brierley, J. Google Scholar, Gupta, R. S. 1998a Lifes third domain (Archaea): an established fact or an endangered paradigm? Biol. Bacteriological Reviews 26:6794. nov., and Acidianus brierleyi comb. Nitrogen-fixing organisms can either exist independently or pair up with a plant host: Assimilation is a reductive process by which an inorganic form of nitrogen is reduced to organic nitrogen compounds such as amino acids and nucleotides, allowing for cellular growth and reproduction. Front Microbiol. Evidence for the presence of phosphoriboisomerase and ribulose-1,5-diphosphate carboxylase in extracts of Desulfovibrio vulgaris. European Journal of Applied Microbiology and Biotechnology 5:291299. 0000004210 00000 n Biology of Thiobacillus ferrooxidans in relation to the microbiological leaching of sulphide ores. This process is experimental and the keywords may be updated as the learning algorithm improves. 129 28472855, Robertson, L. A., Kuenen, J. G. 1991 The colorless sulfur bacteria A. Balows, H. G. Truper, M. Dworkin, W. Harder, and K.-H. Schleifer (ed.s) The prokaryotes, 2nd ed., Springer-Verlag New York NY 385413, Ruby, E. G., Wirsen, C. O., Jannasch, H. W. 1981 Chemolithotrophic sulfur-oxidizing bacteria from the Galapagos rift hydrothermal vents App. 44 19851986, Keil, F. 1912 Beitrge zur Physiologie der farblosen Schwefelbakterien Beitr. 11 157182, van der Graaf, A. Plants, animals, and other organisms rely on bacteria and archaea to provide nitrogen in a fixed form, since no eukaryote is known that can fix nitrogen. Fungal Diversity in Barley Under Different Storage Conditions. These keywords were added by machine and not by the authors. 41 419448, Smock, A. M., Bottcher, M. E., Cypionka, H. 1998 Fractionation of sulfur isotopes during thiosulfate reduction by Desulfovibrio desulfuricans Arch. We use cookies to distinguish you from other users and to provide you with a better experience on our websites. nov., a thermoacidophilic, aerobic, hydrogen-oxidizing bacterium requiring elemental sulfur for growth Int. Soil biochar amendment as a climate change mitigation tool: Key parameters and mechanisms involved. The smaller the distance between the two, the less ATP that will be formed. J. Syst. Microbiol. By oxidizing the compounds, the energy stored in chemical bonds can be utilized in cellular processes. Ihre Lebensprozesse spielen sich nach einem viel einfacheren Schema ab; durch einen rein anorganischen chemischen Prozesswerden alle ihre Lebensbewegungen im Gange erhalten. 0000056599 00000 n 960. Published online by Cambridge University Press: [1] Two types of lithoautotrophs are distinguished by their energy source; photolithoautotrophs derive their energy from light while chemolithoautotrophs (chemolithotrophs or chemoautotrophs) derive their . ber Eisenbacterien. 0000079153 00000 n This process is experimental and the keywords may be updated as the learning algorithm improves. Mikrobiol. Bacterial energetics Academic Press San Diego. J. Syst. The SlideShare family just got bigger. 0000019448 00000 n Chemolithotrophy 12. Archives of Microbiology 118:2126. Encyclopedia.com. Botanische Zeitung 45:489600, 606616. Winogradsky, S., 1887. Download preview PDF. How are different nitrogen compounds used in their metabolism? As with chemoorganotrophs, metabolism of chemolithotrophs requires ATP and NAD(P)H for carbon metabolism and biosynthetic processes. Mikrobiol. Schlegel, H. G. 1975. Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. Pflanzenphysiologie, vol. 1990 Organic sulfur compounds in the environment Adv. CrossRef Iron has a widespread distribution globally and is considered one of the most abundant in the Earth's crust, soil, and sediments. DEEPALI Therefore, be sure to refer to those guidelines when editing your bibliography or works cited list. Archives of Microbiology 108:287292. In: Starr, M.P., Stolp, H., Trper, H.G., Balows, A., Schlegel, H.G. 41 130133, Nishihara, H., Toshiaki, Y., Chung, S. Y., Suzuki, K-I., Yanagi, M., Yamasata, K., Kodama, T., Igarashi, Y. 0000060061 00000 n in oxygen-sulfide gradients Appl. Enjoy access to millions of ebooks, audiobooks, magazines, and more from Scribd. Anyone you share the following link with will be able to read this content: Sorry, a shareable link is not currently available for this article. 180 29752982, Whittenbury, R., Kelly, D. P. 1977 Autotrophy: a conceptual phoenix Symp. Env. Sci. Archives of Microbiology 116:4149. Nutritional types in bacteria: Chemolithotrophy. Bethesda, MD 20894, Web Policies Brock Biology of Microorganisms, 11th edn. Madigan, M., and Martinko, J. Broda, E. 1977a. The role of microorganisms in the weathering of minerals has long been recognized ().More recent interest in the role of Fe(II)-oxidizing bacteria (FeOB) has been driven by the recognition that Fe(II)-bearing mineral phases, such as Fe(II)-silicates and pyrite, represent a potential wealth of energy to fuel chemolithotrophic metabolisms, both terrestrially and on other rocky planetary bodies . We've encountered a problem, please try again. Nitrogen fixation is an extremely energy and electron intensive process, in order to break the triple bond in N2 and reduce it to NH3. Appl. PubMedGoogle Scholar, University of Gttingen, Gttingen, Germany. PubMed Microbiol. FEMS Microbiology Letters 2: 305307. Annual Review of Microbiology 22:489518. Google Scholar. If the molecules are small, as with the elements listed above, they can be utilized by chemolithotrophs. The process is performed by diazotrophs, a limited number of bacteria and archaea that can grow without an external source of fixed nitrogen, because of their abilities. The Chemolithotrophic Prokaryotes. 55 29092917, Nelson, D. C., Williams, C. A., Farah, B. World of Microbiology and Immunology. is added to your Approved Personal Document E-mail List under your Personal Document Settings The obligate autotrophthe demise of a concept. 2264 62 These bacteria are most commonly encountered as the rusty coloured and slimy layer that builds up on the inside of toilet tanks. CAS Chemolithotrophy can occur aerobically or anaerobically. It is particularly important in the high-nutrient, low-chlorophyll regions, where the presence of micronutrients is mandatory for the total primary production.[11]. 1. 0000022625 00000 n 0000006778 00000 n Springer, Dordrecht. The term chemolithotrophy describes the energy metabolism of bacteria that can, in the absence of light, use the oxidation of inorganic substances as a source of energy for cell biosynthesis and maintenance (Rittenberg, 1969). 51 221271, Woese, C. R. 1998 The universal ancestor Proc. 80 501507, Metzdorf, N., Kaltwasser, H. 1988 Utilization of organic compounds as the sole source of nitrogen by Thiobacillus thiooxidans Arch. Microbiol. 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chemolithotrophic bacteria slideshare

chemolithotrophic bacteria slideshare