Bacteria, Fungi and Archaea Domains in Rhizospheric Soil and Their Effects in Enhancing Agricultural Productivity
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Anoxygenic Photosynthesis in Photolithotrophic Sulfur Bacteria and Their Role in Detoxication of Hydrogen Sulfide
antioxidants Review Anoxygenic Photosynthesis in Photolithotrophic Sulfur Bacteria and Their Role in Detoxication of Hydrogen Sulfide Ivan Kushkevych 1,* , Veronika Bosáková 1,2 , Monika Vítˇezová 1 and Simon K.-M. R. Rittmann 3,* 1 Department of Experimental Biology, Faculty of Science, Masaryk University, 62500 Brno, Czech Republic; [email protected] (V.B.); [email protected] (M.V.) 2 Department of Biology, Faculty of Medicine, Masaryk University, 62500 Brno, Czech Republic 3 Archaea Physiology & Biotechnology Group, Department of Functional and Evolutionary Ecology, Universität Wien, 1090 Vienna, Austria * Correspondence: [email protected] (I.K.); [email protected] (S.K.-M.R.R.); Tel.: +420-549-495-315 (I.K.); +431-427-776-513 (S.K.-M.R.R.) Abstract: Hydrogen sulfide is a toxic compound that can affect various groups of water microorgan- isms. Photolithotrophic sulfur bacteria including Chromatiaceae and Chlorobiaceae are able to convert inorganic substrate (hydrogen sulfide and carbon dioxide) into organic matter deriving energy from photosynthesis. This process takes place in the absence of molecular oxygen and is referred to as anoxygenic photosynthesis, in which exogenous electron donors are needed. These donors may be reduced sulfur compounds such as hydrogen sulfide. This paper deals with the description of this metabolic process, representatives of the above-mentioned families, and discusses the possibility using anoxygenic phototrophic microorganisms for the detoxification of toxic hydrogen sulfide. Moreover, their general characteristics, morphology, metabolism, and taxonomy are described as Citation: Kushkevych, I.; Bosáková, well as the conditions for isolation and cultivation of these microorganisms will be presented. V.; Vítˇezová,M.; Rittmann, S.K.-M.R. -
Limits of Life on Earth Some Archaea and Bacteria
Limits of life on Earth Thermophiles Temperatures up to ~55C are common, but T > 55C is Some archaea and bacteria (extremophiles) can live in associated usually with geothermal features (hot springs, environments that we would consider inhospitable to volcanic activity etc) life (heat, cold, acidity, high pressure etc) Thermophiles are organisms that can successfully live Distinguish between growth and survival: many organisms can survive intervals of harsh conditions but could not at high temperatures live permanently in such conditions (e.g. seeds, spores) Best studied extremophiles: may be relevant to the Interest: origin of life. Very hot environments tolerable for life do not seem to exist elsewhere in the Solar System • analogs for extraterrestrial environments • `extreme’ conditions may have been more common on the early Earth - origin of life? • some unusual environments (e.g. subterranean) are very widespread Extraterrestrial Life: Spring 2008 Extraterrestrial Life: Spring 2008 Grand Prismatic Spring, Yellowstone National Park Hydrothermal vents: high pressure in the deep ocean allows liquid water Colors on the edge of the at T >> 100C spring are caused by different colonies of thermophilic Vents emit superheated water (300C or cyanobacteria and algae more) that is rich in minerals Hottest water is lifeless, but `cooler’ ~50 species of such thermophiles - mostly archae with some margins support array of thermophiles: cyanobacteria and anaerobic photosynthetic bacteria oxidize sulphur, manganese, grow on methane + carbon monoxide etc… Sulfolobus: optimum T ~ 80C, minimum 60C, maximum 90C, also prefer a moderately acidic pH. Live by oxidizing sulfur Known examples can grow (i.e. multiply) at temperatures which is abundant near hot springs. -
Community Assembly and Coexistence in Communities of Arbuscular Mycorrhizal Fungi
The ISME Journal (2016) 10, 2341–2351 OPEN © 2016 International Society for Microbial Ecology All rights reserved 1751-7362/16 www.nature.com/ismej MINI REVIEW Community assembly and coexistence in communities of arbuscular mycorrhizal fungi Kriszta Vályi1,2, Ulfah Mardhiah1,2, Matthias C Rillig1,2 and Stefan Hempel1,2 1Department of Plant Ecology, Institut für Biologie, Freie Universität Berlin, Berlin, Germany and 2Berlin- Brandenburg Institute of Advanced Biodiversity Research, Berlin, Germany Arbuscular mycorrhizal fungi are asexual, obligately symbiotic fungi with unique morphology and genomic structure, which occupy a dual niche, that is, the soil and the host root. Consequently, the direct adoption of models for community assembly developed for other organism groups is not evident. In this paper we adapted modern coexistence and assembly theory to arbuscular mycorrhizal fungi. We review research on the elements of community assembly and coexistence of arbuscular mycorrhizal fungi, highlighting recent studies using molecular methods. By addressing several points from the individual to the community level where the application of modern community ecology terms runs into problems when arbuscular mycorrhizal fungi are concerned, we aim to account for these special circumstances from a mycocentric point of view. We suggest that hierarchical spatial structure of arbuscular mycorrhizal fungal communities should be explicitly taken into account in future studies. The conceptual framework we develop here for arbuscular mycorrhizal fungi is also adaptable for other host-associated microbial communities. The ISME Journal (2016) 10, 2341–2351; doi:10.1038/ismej.2016.46; published online 19 April 2016 Introduction: applying models of which the members of local communities are selected community assembly and contemporary by passing through environmental and biotic filters. -
Marine-Derived Fungal Siderophores: a Perception
Indian Journal of Geo-Marine Science Vol. 45(3) March 2016, pp. 431-439 Marine-derived Fungal Siderophores: A Perception Hiral B. Trivedi, Anjana K. Vala, Jaykishan H. Dhrangadhriya & Bharti P. Dave* Department of Life Sciences, Maharaja Krishnakumarsinhji Bhavnagar University, Sardar Vallabhbhai Patel Campus, Bhavnagar-364 001, Gujarat, India [E-mail: [email protected]] Received 25August 2014; revised 01 October 2014 Siderophores play crucial role in biogeochemical cycle in terrestrial as well as marine environment. Siderophores of bacteria from marine habitats have been extensively studied, however, comparatively less information is available on their fungal counter parts. This review focuses on siderophores of marine-derived fungi, molecular mechanism of siderophore biosynthesis and their uptake. Their chemical nature and applications are also discussed. Data so far available on marine fungal siderophores are found to be very interesting. Though less explored, the information available reveals novelty in chemical nature of siderophores of marine-derived fungi, i.e. occurrence of catecholates in fungi and carboxylates in non- mucoraceous fungi, which is the first-ever report. Further investigations on marine-derived fungal siderophores would be an interesting area of research. [Key words: Siderophore, Marine-derived fungi, Catecholate, Carboxylate, Hydroxamate] Introduction low iron concentration affecting the primary production. Marine microorganisms affected by Iron is an essential macronutrient for the growth this critical situation cope up with this stressing of microorganisms. It plays crucial role in condition by producing siderophores to gain iron various cellular processes like DNA/RNA in HNLC regions [9-19]. While much work is synthesis, ATP synthesis, respiration and also as done on bacterial siderophores from marine [1] a cofactor of numerous enzymes . -
Screening and Characterization of Siderophore Producing Endophytic Bacteria from Cicer Arietinum and Pisum Sativum Plants
Journal of Applied Biology & Biotechnology Vol. 7(05), pp. 7-14, Sep-Oct, 2019 Available online at http://www.jabonline.in DOI: 10.7324/JABB.2019.70502 Screening and characterization of siderophore producing endophytic bacteria from Cicer arietinum and Pisum sativum plants Rajat Maheshwari, Namita Bhutani, Pooja Suneja* Department of Microbiology, Maharshi Dayanand University, Rohtak 124001, India ARTICLE INFO ABSTRACT Article history: Siderophores are low molecular weight iron chelating secondary metabolites synthesized by various groups Received on: March 10, 2019 of microorganisms help in scavenging iron-limited conditions. Siderophores produced by endophytic bacteria Accepted on: April 26, 2019 facilitate the plant growth by providing iron to plants. The objective of this study was to isolate and screen Available online: September 10, 2019 the siderophore producing endophytes from nodules and roots of Cicer arietinum and Pisum sativum plants. Out of total 84 isolates, only 14 endophytes produced siderophore and quantitative analysis was also done. Ten best siderophore producers (above 65% siderophore units) were characterized for the type of siderophore Key words: produced. Most of them were producing hydroxamate and carboxylate type of siderophores. These 10 isolates Endophytes, plant growth were evaluated for other plant growth promoting (PGP) traits in vitro. All of them were producing ammonia promotion, siderophore, CAS and indole-3-acetic acid (IAA). Isolate CPFR10 was found to be positive for all the PGP traits viz. ammonia, assay, tetrazolium, hydroxamate organic acid, HCN, and IAA production. Diversity analysis of these 10 isolates using Amplified rDNA Restriction Analysis profile revealed nine genotypes at 90% similarity. 1. INTRODUCTION in acquiring mineral nutrients, function as virulence factors to Iron is the fourth most abundant element in the Earth’s crust, vital protect them from pathogens [6,7]. -
The Effects of Iron Supplementation and Fortification on the Gut Microbiota: a Review
Review The Effects of Iron Supplementation and Fortification on the Gut Microbiota: A Review Emma CL Finlayson-Trick 1 , Jordie AJ Fischer 2,3 , David M Goldfarb 1,3,4 and Crystal D Karakochuk 2,3,* 1 Faculty of Medicine, University of British Columbia, Vancouver, BC V6T 1Z3, Canada; efi[email protected] (E.C.F.-T.); [email protected] (D.M.G.) 2 Department of Food, Nutrition and Health, University of British Columbia, Vancouver, BC V6T 1Z4, Canada; jordie.fi[email protected] 3 British Columbia Children’s Hospital Research Institute, Vancouver, BC V5Z 4H4, Canada 4 Department of Pathology and Laboratory Medicine, BC Children’s and Women’s Hospital and University of British Columbia, Vancouver, BC V6T 1Z7, Canada * Correspondence: [email protected] Received: 30 August 2020; Accepted: 24 September 2020; Published: 26 September 2020 Abstract: Iron supplementation and fortification are used to treat iron deficiency, which is often associated with gastrointestinal conditions, such as inflammatory bowel disease and colorectal cancer. Within the gut, commensal bacteria contribute to maintaining systemic iron homeostasis. Disturbances that lead to excess iron promote the replication and virulence of enteric pathogens. Consequently, research has been interested in better understanding the effects of iron supplementation and fortification on gut bacterial composition and overall gut health. While animal and human trials have shown seemingly conflicting results, these studies emphasize how numerous factors influence gut microbial composition. Understanding how different iron formulations and doses impact specific bacteria will improve the outcomes of iron supplementation and fortification in humans. Furthermore, discerning the nuances of iron supplementation and fortification will benefit subpopulations that currently do not respond well to treatment. -
Siderophores from Marine Bacteria with Special Emphasis on Vibrionaceae
Archana et al Int. J. Pure App. Biosci. 7 (3): 58-66 (2019) ISSN: 2320 – 7051 Available online at www.ijpab.com DOI: http://dx.doi.org/10.18782/2320-7051.7492 ISSN: 2320 – 7051 Int. J. Pure App. Biosci. 7 (3): 58-66 (2019) Review Article Siderophores from Marine Bacteria with Special Emphasis on Vibrionaceae Archana V.1, K. Revathi2*, V. P. Limna Mol3, R. Kirubagaran3 1Department of Advanced Zoology and Biotechnology, Madras University, Chennai- 600005 2MAHER University, Chennai, Tamil Nadu – 600078 3Ocean Science and Technology for Islands, National Institute of Ocean Technology (NIOT), Ministry of Earth Sciences, Government of India, Pallikaranai, Chennai- 600100 *Corresponding Author E-mail: [email protected] Received: 11.04.2019 | Revised: 18.05.2019 | Accepted: 25.05.2019 ABSTRACT More than 500 siderophores have been isolated from a huge number of marine bacteria till date. With mankind’s ever-increasing search for novel molecules towards industrial and medical applications, siderophores have gained high importance. These chelating ligands have immense potential in promoting plant growth, drug-delivery, treatment of iron-overload, etc. Many of the potential siderophores have been isolated from bacteria like Pseudomonas, Bacillus, Nocardia, etc. Bacteria belonging to the family Vibrionaceae have recently gained focus owing to their rich potential in secreting siderophores. Many of the vibrionales, viz. Vibrio harveyii, V. anguillarium, V. campbellii. etc. are aquatic pathogens. These bacteria require iron for their growth and virulence, and hence produce a wide variety of siderophores. The genetic basis of siderophore production by Vibrio sp. has also been largely studied. Further detailed genetic analysis of the mode of siderophore production by Vibrionaceae would be highly effective to treat aquaculture diseases caused by these pathogenic organisms. -
The Unicellular and Colonial Organisms Prokaryotic And
The Unicellular and Colonial Organisms Prokaryotic and Eukaryotic Cells As you know, the building blocks of life are cells. Prokaryotic cells are those cells that do NOT have a nucleus. They mostly include bacteria and archaea. These cells do not have membrane-bound organelles. Eukaryotic cells are those that have a true nucleus. That would include plant, animal, algae, and fungal cells. As you can see, to the left, eukaryotic cells are typically larger than prokaryotic cells. Today in lab, we will look at examples of both prokaryotic and eukaryotic unicellular organisms that are commonly found in pond water. When examining pond water under a microscope… The unpigmented, moving microbes will usually be protozoans. Greenish or golden-brown organisms will typically be algae. Microorganisms that are blue-green will be cyanobacteria. As you can see below, living things are divided into 3 domains based upon shared characteristics. Domain Eukarya is further divided into 4 Kingdoms. Domain Kingdom Cell type Organization Nutrition Organisms Absorb, Unicellular-small; Prokaryotic Photsyn., Archaeacteria Archaea Archaebacteria Lacking peptidoglycan Chemosyn. Unicellular-small; Absorb, Bacteria, Prokaryotic Peptidoglycan in cell Photsyn., Bacteria Eubacteria Cyanobacteria wall Chemosyn. Ingestion, Eukaryotic Unicellular or colonial Protozoa, Algae Protista Photosynthesis Fungi, yeast, Fungi Eukaryotic Multicellular Absorption Eukarya molds Plantae Eukaryotic Multicellular Photosynthesis Plants Animalia Eukaryotic Multicellular Ingestion Animals Prokaryotic Organisms – the archaea, non-photosynthetic bacteria, and cyanobacteria Archaea - Microorganisms that resemble bacteria, but are different from them in certain aspects. Archaea cell walls do not include the macromolecule peptidoglycan, which is always found in the cell walls of bacteria. Archaea usually live in extreme, often very hot or salty environments, such as hot mineral springs or deep-sea hydrothermal vents. -
Archaeal Distribution and Abundance in Water Masses of the Arctic Ocean, Pacific Sector
Vol. 69: 101–112, 2013 AQUATIC MICROBIAL ECOLOGY Published online April 30 doi: 10.3354/ame01624 Aquat Microb Ecol FREEREE ACCESSCCESS Archaeal distribution and abundance in water masses of the Arctic Ocean, Pacific sector Chie Amano-Sato1, Shohei Akiyama1, Masao Uchida2, Koji Shimada3, Motoo Utsumi1,* 1University of Tsukuba, Tennodai, Tsukuba, Ibaraki 305-8572, Japan 2National Institute for Environmental Studies, Onogawa, Tsukuba, Ibaraki 305-8506, Japan 3Tokyo University of Marine Science and Technology, Konan, Minato-ku, Tokyo 108-8477, Japan ABSTRACT: Marine planktonic Archaea have been recently recognized as an ecologically impor- tant component of marine prokaryotic biomass in the world’s oceans. Their abundance and meta- bolism are closely connected with marine geochemical cycling. We evaluated the distribution of planktonic Archaea in the Pacific sector of the Arctic Ocean using fluorescence in situ hybridiza- tion (FISH) with catalyzed reporter deposition (CARD-FISH) and performed statistical analyses using data for archaeal abundance and geochemical variables. The relative abundance of Thaum - archaeota generally increased with depth, and euryarchaeal abundance was the lowest of all planktonic prokaryotes. Multiple regression analysis showed that the thaumarchaeal relative abundance was negatively correlated with ammonium and dissolved oxygen concentrations and chlorophyll fluorescence. Canonical correspondence analysis showed that archaeal distributions differed with oceanographic water masses; in particular, Thaumarchaeota were abundant from the halocline layer to deep water, where salinity was higher and most nutrients were depleted. However, at several stations on the East Siberian Sea side of the study area and along the North- wind Ridge, Thaumarchaeota and Bacteria were proportionally very abundant at the bottom in association with higher nutrient conditions. -
Oceans of Archaea Abundant Oceanic Crenarchaeota Appear to Derive from Thermophilic Ancestors That Invaded Low-Temperature Marine Environments
Oceans of Archaea Abundant oceanic Crenarchaeota appear to derive from thermophilic ancestors that invaded low-temperature marine environments Edward F. DeLong arth’s microbiota is remarkably per- karyotes), Archaea, and Bacteria. Although al- vasive, thriving at extremely high ternative taxonomic schemes have been recently temperature, low and high pH, high proposed, whole-genome and other analyses E salinity, and low water availability. tend to support Woese’s three-domain concept. One lineage of microbial life in par- Well-known and cultivated archaea generally ticular, the Archaea, is especially adept at ex- fall into several major phenotypic groupings: ploiting environmental extremes. Despite their these include extreme halophiles, methanogens, success in these challenging habitats, the Ar- and extreme thermophiles and thermoacido- chaea may now also be viewed as a philes. Early on, extremely halo- cosmopolitan lot. These microbes philic archaea (haloarchaea) were exist in a wide variety of terres- first noticed as bright-red colonies trial, freshwater, and marine habi- Archaea exist in growing on salted fish or hides. tats, sometimes in very high abun- a wide variety For many years, halophilic isolates dance. The oceanic Marine Group of terrestrial, from salterns, salt deposits, and I Crenarchaeota, for example, ri- freshwater, and landlocked seas provided excellent val total bacterial biomass in wa- marine habitats, model systems for studying adap- ters below 100 m. These wide- tations to high salinity. It was only spread Archaea appear to derive sometimes in much later, however, that it was from thermophilic ancestors that very high realized that these salt-loving invaded diverse low-temperature abundance “bacteria” are actually members environments. -
Ionizing Radiation: How Fungi Cope, Adapt, and Exploit with the Help of Melanin Ekaterina Dadachova1 and Arturo Casadevall2
Available online at www.sciencedirect.com Ionizing radiation: how fungi cope, adapt, and exploit with the help of melanin Ekaterina Dadachova1 and Arturo Casadevall2 Life on Earth has always existed in the flux of ionizing radiation. life forms. Large quantities of highly melanized fungal However, fungi seem to interact with the ionizing radiation spores have been found in early Cretaceous period depos- differently from other inhabitants of the Earth. Recent data its when many species of animals and plants died out. show that melanized fungal species like those from This period coincides with Earth’s crossing the ‘magnetic Chernobyl’s reactor respond to ionizing radiation with zero’ resulting in the loss of its ‘shield’ against cosmic enhanced growth. Fungi colonize space stations and adapt radiation [2]. Additionally, it has been suggested that morphologically to extreme conditions. Radiation exposure radiation from a putative passing star called Nemesis causes upregulation of many key genes, and an inducible might have contributed to extinction events [3]. Fungi microhomology-mediated recombination pathway could be a in general, and especially melanized ones, are highly potential mechanism of adaptive evolution in eukaryotes. The radioresistant when subjected to high doses of ionizing discovery of melanized organisms in high radiation radiation under experimental conditions [4–7]. Under- environments, the space stations, Antarctic mountains, and in standably, such unusual abilities of eukaryotes to survive the reactor cooling water combined with phenomenon of or maybe even benefit from exposure to ionizing radiation ‘radiotropism’ raises the tantalizing possibility that melanins are in contrast to the general view that radiation is have functions analogous to other energy harvesting pigments uniformly harmful to life. -
Occurrence of Mycorrhizae in Some Species of Carex (Cyperaceae) of the Darjeeling Himalayas, India
Research Article ISSN 2250-0480 VOL 4/ISSUE 1/JAN-MAR 2014 OCCURRENCE OF MYCORRHIZAE IN SOME SPECIES OF CAREX (CYPERACEAE) OF THE DARJEELING HIMALAYAS, INDIA *ASOK GHOSH 1, SHEKHAR BHUJEL 2 AND GAUR GOPAL MAITI 3 *1Department of Botany, Krishnagar Govt. College, Nadia, West Bengal, India 2Department of Botany, Darjeeling Govt. College, Darjeeling, West Bengal, India (Presently DTR&DC, Tea Board, A.B. Path, Kurseong, West Bengal, India) 3Department of Botany, University of Kalyani, Kalyani, West Bengal, India ABSTRACT The Cyperaceae (sedge family) have generally been considered non-mycorrhizal, although recent evidences suggest that mycotrophy may be considerably more widespread among sedges than was previously realized. In this study, 28 in situ populations of 12 species of Carex L.(C. myosurus Nees, C. composita Boott, C. cruciata Wahl., C. filicina Nees, C. inanis Kunth, C. setigera D. Don, C. insignis Boott, C. finitima var. finitima; C. fusiformis Nees subsp. finitima (Boott) Noltie, C. teres Boott, C. longipes D. Don ex Tilloch and Taylor, C. nubigena D. Don ex Tilloch and Taylor and C. rochebrunii subsp. rochebrunii; C. remota Linnaeus subsp. rochebrunii (Franchet and Savatier) Kükenthal) occurring in the Darjeeling Himalayas were surveyed. Mycorrhizal infection by VAM (Vesicular Arbuscular Mycorrhiza) fungi was found in roots of 9 species (C. myosurus, C. composita, C. cruciata, C. filicina, C. inanis, C. setigera, C. finitima, C. teres, and C. nubigena ) and appears to occur in response to many factors, both environmental and phylogenetic. In non-mycorrhizal species, a novel root character, the presence of bulbous-based root hairs, was identified. Key words: Carex, Cyperaceae, vesicular arbuscular mycorrhiza (VAM), mycotrophy, root hairs 1.