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  • 1
    Online Resource
    Online Resource
    Cham :Springer International Publishing AG,
    Keywords: Marine biotechnology. ; Electronic books.
    Type of Medium: Online Resource
    Pages: 1 online resource (621 pages)
    Edition: 1st ed.
    ISBN: 9783319690759
    Series Statement: Grand Challenges in Biology and Biotechnology Series
    DDC: 660.6
    Language: English
    Note: Intro -- Foreword -- Preface -- Introduction -- The Promise of the Blue Biotechnology -- The Economic Potential of Marine Biotechnology -- Supporting the Development of Marine Biotechnology -- Conclusions and Perspectives -- Contents -- About the Editors -- Part I: The Promise of the Blue Biotechnology -- Chapter 1: The Marine Ecosystem as a Source of Antibiotics -- 1 Introduction -- 2 Marine Cyanobacteria and Bacteria -- 2.1 Cyanobacteria -- 2.2 Bacteria -- 3 Marine Fungi -- 4 Sponge -- 5 Cnidaria -- 6 Bryozoa -- 7 Mollusca -- 8 Annelida -- 9 Echinodermata -- 10 Tunicate -- 11 Marine Algae -- 12 Conclusions -- References -- Chapter 2: Seaweeds: Valuable Ingredients for the Pharmaceutical Industries -- 1 Introduction -- 2 Polysaccharides of Seaweeds -- 2.1 Ulvan -- 2.2 Agar and Carrageenan -- 2.3 Alginate, Fucoidan, and Laminaran -- 2.4 Bioactivity and Pharmaceutical Value of Seaweeds Polysaccharides -- 2.4.1 Antiviral and Antibacterial Activities -- 2.4.2 Anti-inflammatory and Immunomodulatory Activities -- 2.4.3 Anticoagulant and Antithrombotic Activities -- 2.4.4 Anticancer Activities -- 3 Pigments of Seaweeds -- 3.1 Antioxidant Activity of Seaweeds Pigments -- 3.2 Anti-inflammatory Activity of Seaweeds Pigments -- 3.3 Neuroprotective Activity of Seaweeds Pigments -- 4 Phlorotannin -- 4.1 Antioxidant Activity of Phlorotannins -- 4.2 Bactericidal Activity of Phlorotannins -- 4.3 Anticancer Activity of Phlorotannins -- 4.4 Antidiabetic Activity of Phlorotannins -- 4.5 Antiallergic Activity of Phlorotannins -- 4.6 Anti-inflammatory Activities of Phlorotannins -- 5 Seaweed Bioactive Peptides -- 5.1 Antioxidant Activity of Seaweed-Derived Peptides -- 5.2 Antihypertensive Activity of Seaweed-Derived Peptides -- 5.3 Immunomodulatory Effects of Seaweed-Derived Peptides -- 6 Seaweed Vitamins -- 7 Seaweed Minerals -- 8 Conclusions -- References. , Chapter 3: Anti-infective Compounds from Marine Organisms -- 1 Introduction -- 2 Antibacterial Compounds -- 2.1 From Bacteria -- 2.2 From Fungi -- 2.3 From Algae -- 2.4 From Invertebrates -- 3 Antifungal Compounds -- 3.1 From Bacteria -- 3.2 From Fungi -- 3.3 From Invertebrates -- 4 Antiviral Compounds -- 4.1 From Fungi -- 4.2 From Algae -- 4.3 From Invertebrates -- 5 Antiprotozoal Compounds -- 5.1 From Bacteria -- 5.2 From Algae -- 5.3 From Invertebrates -- 6 Conclusions -- References -- Chapter 4: The Marine-Derived Filamentous Fungi in Biotechnology -- 1 Introduction -- 2 General Outline of Marine Fungi -- 3 Habitats and Diversity of Marine Fungi -- 4 Secondary Metabolites -- 5 Polysaccharides -- 6 Enzymes -- 6.1 Enzymes Used in the Pharmaceutical, Cosmetic and Food Industries -- 6.2 Biofuels -- 6.3 Enzymes Used in the Textile and Paper Industries -- 6.4 Enzymes for Environmental Applications -- 7 Bioremediation -- 8 Nanotechnologies -- 9 Future Perspectives -- References -- Chapter 5: Aplysinopsins as Promising Marine Natural Product Drug Leads: Recent Developments -- 1 Introduction -- 2 Aplysinopsins -- 3 Synthesis of Aplysinopsin Analogs -- 3.1 Thioaplysinopsin Analogs -- 3.2 Pentamidine-Aplysinopsin Synthesis -- 3.3 Microwave-Assisted Synthesis of Aplysinopsins -- 3.4 Recyclization of Oxazolones into Aplysinopsins -- 4 Biological Activities of Aplysinopsins -- 4.1 Antiplasmodial and Antileishmanial Activity -- 4.2 CNS Activity -- 4.2.1 Serotonin Receptor Activity -- 4.2.2 Monoamine Oxidase Inhibition -- 4.3 Anticancer Activities -- 4.4 Glycine-Gated Chloride Channel Receptor Modulation -- 4.5 In Vivo Studies -- 5 Summary -- References -- Chapter 6: Potential of Hydrogen Fermentative Pathways in Marine Thermophilic Bacteria: Dark Fermentation and Capnophilic Lact... -- 1 Introduction -- 2 Species and Culture Conditions -- 2.1 Taxonomy. , 2.2 Strain Origin -- 2.3 Culture Conditions -- 3 Fermentative Hydrogen Production by T. neapolitana -- 3.1 Dark Fermentation (DF) by T. neapolitana -- 3.2 Capnophilic Lactic Fermentation (CLF) by T. neapolitana -- 4 Anaerobic Sugar Fermentation in Thermotoga and Pseudothermotoga Genera -- 4.1 Bacterial Growth and Tolerance to CO2 -- 4.2 Glucose Consumption and Hydrogen Yield Under N2 and CO2 Conditions -- 4.3 Organic Metabolite Production Under N2 and CO2 Conditions -- 5 Challenges -- 6 Conclusions -- References -- Chapter 7: Anaerobic Digestion and Gasification of Seaweed -- 1 Introduction -- 2 Method of Converting Seaweed to Biofuels -- 2.1 Seaweed as a Feedstock -- 2.2 Dewatering and Drying Macroalgae -- 2.3 Direct Combustion -- 2.4 Biodiesel -- 2.5 Bioethanol -- 2.6 Biobutanol -- 2.7 Hydrothermal Processing -- 3 Gasification and Anaerobic Digestion -- 3.1 Gasification -- 3.2 Anaerobic Digestion -- 4 Conclusions -- References -- Part II: The Economic Potential of Marine Biotechnology -- Chapter 8: The Global Market for Marine Biotechnology: The Underwater World of Marine Biotech Firms -- 1 Introduction -- 2 Blue Biotechnology: A Definition -- 3 The Blue Biotechnology Industries -- 3.1 Cosmetics -- 3.2 Pharmaceuticals -- 3.3 Food, Feed, and Nutraceuticals -- 3.4 Energy -- 3.5 Bio-Based Chemicals -- 4 The Analysis of a Sample of Firms -- 4.1 Methodology -- 4.2 Discussion -- 5 Conclusions -- References -- Chapter 9: How to Succeed in Marketing Marine Natural Products for Nutraceutical, Pharmaceutical and Cosmeceutical Markets -- 1 Introduction -- 1.1 Marine Natural Products: A Historical and Taxonomic Perspective -- 1.2 MNP Discovery and Development -- 2 Marine Natural Products and Value Chains -- 2.1 Nutraceutical Marine Natural Products -- 2.1.1 Marine Lipids -- 2.1.2 Fish Proteins -- 2.1.3 Fish Protein Hydrolysates. , 2.1.4 Marine Bioactive Peptides -- 2.1.5 Chitin, Chitosan and Related Compounds -- 2.1.6 Marine Polysaccharides -- 2.1.7 Marine Carotenoids -- 2.1.8 Other Relevant Compounds -- 2.2 Pharmaceutical Marine Natural Products -- 2.2.1 Marketed Marine Drugs and Close Analogues in Clinical Trials -- Cytarabine (Cytosar-U -- Depocyte), Vidarabine (Vira-A), Fludarabine Phosphate (Fludara) and Nelarabine (Arranon/Atriance) -- Ziconotide (Prialt) -- Fish n-3 Fatty Acid Derivatives (Omacor/Lovaza) -- Trabectedin (Yondelis) and Lurbinectedin -- Eribulin Mesylate (Halaven) -- Brentuximab Vedotin (Adcetris) and Close Analogues -- Iota Carrageenans (Carragelose) -- 2.2.2 Marine Natural Products and Close Analogues in Development -- 2.3 Cosmeceutical Marine Natural Products -- 2.3.1 Seaweed-Based Ingredients -- Classical Seaweed-Based Ingredients -- Biotechnology-Based Seaweed Ingredients -- 2.3.2 Microalgae Biotechnology-Based Ingredients -- 2.3.3 Specialty Biotechnology-Derived Active Ingredients -- The First Commercial Success: Abyssine by Unipex (New York, NY, USA) -- A Very Strong Brand Successful Marine Line: Resilience by Estée Lauder (New York, NY, USA) -- Recent Innovations and Marine Biotech Role: Nocturshape, Cellynkage and SeaCode by Lipotec (Barcelona, Spain) -- 2.3.4 Other Non-premium-Derived Marine Bioactive Ingredients -- 3 Major Challenges and Suggestions for Success in MNP Development -- 3.1 Nutraceutical-Specific Challenges -- 3.2 Pharmaceutical-Specific Challenges -- 3.3 Cosmeceutical-Specific Challenges -- 4 Conclusions -- References -- Chapter 10: The European Marine Biological Research Infrastructure Cluster: An Alliance of European Research Infrastructures t... -- 1 Marine Biotechnology: An Emerging Field -- 2 The European Marine Biological Resource Centre (EMBRC), a Pan-European Research Infrastructure in Marine Biology and Ecology. , 2.1 The Genesis and Scope of EMBRC -- 2.2 Links of EMBRC with Maritime Regions -- 3 The Rationale for the European Marine Biological Research Infrastructure Cluster (EMBRIC) -- 3.1 Contribution of Other Pan-European Research Infrastructures to the Development of the Blue Bioeconomy -- 3.2 Objectives and Scope of EMBRIC -- 3.3 Organization of Workflows at EMBRC Facilities -- 4 EMBRIC: An Instrument to Promote the Blue Bioeconomy -- 4.1 Organization of Innovation Clusters at EMBRC Facilities -- 4.2 The Need for Public and Private Investments at Various Scales -- 5 Conclusions -- References -- Part III: Supporting the Development of Marine Biotechnology -- Chapter 11: Grand Challenges in Marine Biotechnology: Overview of Recent EU-Funded Projects -- 1 Introduction -- 2 BAMMBO and MaCuMBA -- 3 GIAVAP and SUNBIOPATH -- 4 BlueGenics, LIPOYEASTS, MAMBA and PolyModE -- 5 SeaBioTech -- 6 MAREX and PharmaSea -- 7 ERA-NET MarineBiotech -- 8 Horizon 2020 Projects -- 9 Conclusions -- References -- Chapter 12: SeaBioTech: From Seabed to Test-Bed: Harvesting the Potential of Marine Biodiversity for Industrial Biotechnology -- 1 Introduction -- 1.1 SeaBioTech Has Put Together a Marine Biodiscovery Pipeline Using an Integrated Approach -- 1.2 SeaBioTech Is an Industry-Driven Project -- 1.3 Identification of Industry Needs: Providing an Industry-Driven Project -- 2 Methodology and Overall Strategy -- 3 The SME Partners and Their Activities -- 3.1 Prokazyme (PKZ) -- 3.2 PHARMAQ -- 3.3 Marine Biopolymers Ltd (MBL) -- 3.4 Ingenza (IGZ) -- 3.5 Horizon Discovery Ltd (HDL) -- 3.6 AXXAM -- 4 Addressing the Challenges Through Scientific Breakthroughs -- 4.1 Challenge 1: Access, Sampling, Storage and Quality Maintenance of Marine Resources Present in Extreme Environments and Spo... -- 4.1.1 Geothermal Intertidal Biotopes in Iceland. , 4.1.2 Deep-Sea Oligotrophic Basins and Hydrothermal Vent Fields in the Eastern Mediterranean Sea.
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  • 2
    Online Resource
    Online Resource
    Milton :Taylor & Francis Group,
    Keywords: Electronic books.
    Description / Table of Contents: This book provides an overview of recent advances in research and technologies related to marine oligosaccharides and polysaccharides. These molecules have important applications in biotherapeutics, foods, cosmetics, environmental protection, and wastewater management.
    Type of Medium: Online Resource
    Pages: 1 online resource (552 pages)
    Edition: 1st ed.
    ISBN: 9780429608438
    DDC: 572.566
    Language: English
    Note: Cover -- Half Title -- Title Page -- Copyright Page -- Contents -- Preface -- Introduction -- Acknowledgments -- Editor -- Contributors -- Section 1: General view and sources of marine polysaccharides and oligosaccharides -- Chapter 1: Marine biodiversity as a new source of promising polysaccharides: innovative polysaccharides emerging from the marine biodiversity -- Contents -- 1.1. Diversity of marine ecosystems -- 1.1.1. Deep-sea environments -- 1.1.2. Shallow submarine thermal springs -- 1.1.3. Tropical environments -- 1.1.4. Arctic and antarctic oceans -- 1.2. Diversity of marine bioresources -- 1.2.1. Marine macroresources -- 1.2.2. Marine microresources -- 1.3. Diversity of marine polysaccharides and their biological activities -- 1.3.1. Chitin/chitosan -- 1.3.2. Galactans and carrageenans -- 1.3.3. Alginates -- 1.3.4. Fucoidans -- 1.3.5. Fungal polysaccharides -- 1.3.6. Microalgal polysaccharides -- 1.3.7. Bacterial polysaccharides -- Summary -- References -- Chapter 2: Applications of marine polysaccharides in food processing -- Contents -- 2.1. Introduction -- 2.2. Major sources of marine polysaccharides and their isolation -- 2.2.1. Crustaceans -- 2.2.2. Seaweeds -- 2.2.3. Microalgae -- 2.2.4. Marine microorganisms -- 2.3. Functionality of polysaccharides in food processing -- 2.4. Food applications of marine polysaccharides -- 2.4.1. Crustacean polysaccharides: chitin, chitosan, and their derivatives -- 2.4.2. Seaweed polysaccharides -- 2.4.3. Polysaccharides from microalgal and marine microorganisms -- 2.5. Polysaccharide-based edible films and coatings -- 2.6. Marine oligosaccharides -- 2.7. Enzymatic processes for marine polysaccharides -- Conclusions -- References -- Chapter 3: The manufacture, characterization, and uses of fucoidans from macroalgae -- Contents -- 3.1. Introduction -- 3.2. Sources of fucoidan. , 3.2.1. Brown seaweeds -- 3.2.2. Echinoderms -- 3.3. Methods for fucoidan extraction -- 3.4. Industry standards: Is it fucoidan? -- 3.5. Quantifying and identifying fucoidan in biological fluids -- 3.6. Fucoidan applications -- 3.6.1. Food supplements -- 3.6.2. Pharmaceuticals -- 3.6.3. Biomaterials -- 3.6.4. Cosmetics -- 3.6.5. Animal applications -- 3.6.6. Agricultural applications -- 3.7. Safety and regulation for use in food and supplements -- Summary -- References -- Chapter 4: Chemical and biological routes for the valorization of macroalgal polysaccharides -- Contents -- 4.1. Introduction -- 4.2. Macroalgal polysaccharides -- 4.3. Functional properties and applications of native macroalgal polysaccharides -- 4.4. Chemical modifications of macroalgal polysaccharides -- 4.5. Catalysts for valorization of macroalgal polysaccharides -- 4.5.1. Chemical catalysts -- 4.5.2. Biological catalysts -- 4.6. Biotransformation of monosugars derived from macroalgal polysaccharides -- Conclusion -- References -- Chapter 5: Marine exopolysaccharides provide protection in extreme environments -- Contents -- 5.1. Introduction -- 5.2. Protection provided by EPS -- 5.2.1. Cryoprotection -- 5.2.2. Protection from high temperature -- 5.2.3. Protection from light -- 5.3. Application potential of marine EPS -- 5.3.1. Bioremediation -- Conclusions -- Acknowledgments -- References -- Chapter 6: Structural mechanisms involved in mild-acid hydrolysis of a defined tetrasaccharide-repeating sulfate fucan -- Contents -- 6.1. Introduction -- 6.2. Specificity of mild-acid hydrolysis on marine invertebrate SFs and SGs -- 6.3. Understanding the process of mild-acid hydrolysis on L. variegatus SF -- 6.4. Structure of products obtained from mild-acid hydrolysis of L. variegatus SF -- 6.5. Confirming 2-desulfation during mild-acid hydrolysis of L. variegatus SF. , 6.6. Glycosidic linkage of the desulfated unit is cleaved during mild-acid hydrolysis of L. variegatus SF -- 6.7. Events underlying mild-acid hydrolysis of L. variegatus SF -- 6.8. Determining the molecular weights of products obtained from mild-acid hydrolysis of L. variegatus SF -- 6.9. Impact of sulfation pattern on the underlying events of mild-acid hydrolysis of L. variegatus SF -- Concluding Remarks -- References -- Chapter 7: Biosynthesis and extrusion of β-chitin nanofibers by diatoms -- Contents -- 7.1. Introduction -- 7.2. Morphology of extracellular diatom chitin nanofibers -- 7.3. Cellular and molecular processes for chitin biosynthesis and nanofiber formation -- 7.3.1. Silica biomineralization and frustule cell wall formation -- 7.3.2. Photosynthetic carbon and nitrogen assimilation -- 7.3.3. Chitin biosynthesis -- 7.3.4. Chitin nanofiber extrusion -- 7.3.5. Molecular genetic basis of chitin biosynthesis and degradation in diatoms -- 7.3.6. Ecological role of extracellular diatom chitin nanofibers -- 7.4. Bioreactor production of chitin nanofibers -- 7.5. Emerging applications of diatom-derived β-chitin nanofibers -- 7.5.1. Unique features of β-chitin nanofibers produced by diatoms -- 7.5.2. Biomedical materials derived from β-chitin nanofibers -- 7.5.3. Potential of β-chitin nanofibers as nanowires for protonic devices -- 7.6. Future research -- Concluding remarks -- Acknowledgments -- References -- Chapter 8: The mucus of marine invertebrates: Cnidarians, polychaetes, and echinoderms as case studies -- Contents -- 8.1. Introduction -- 8.2. Mucus characteristics and structure -- 8.3. Mucus as a food source for bacteria -- 8.4. Mucus as a microenvironment created by the hosts -- 8.5. Mucus antibacterial activity -- 8.6. Other roles of mucus -- Conclusion -- References. , Chapter 9: Biorefinery of unique polysaccharides from Laminaria sp., Kappaphycus sp., and Ulva sp.: structure, enzymatic hydrolysis, and bioenergy from released monosaccharides -- Contents -- 9.1. Introduction -- 9.2. Sources of marine polysaccharides from Laminaria sp, Kappaphycus sp, and Ulva sp. -- 9.2.1. History of seaweed cultivation systems -- 9.2.2. Seaweed-based biorefineries -- 9.2.3. A biorefinery based on Ulva sp.: a case study -- 9.2.4. Polysaccharide extraction and purification methods -- 9.3. Seaweed polysaccharides: structures, applications, and seaweed-associated bacteria as a factor in biorefinery improvement -- 9.3.1. Structures of alginate, carrageenan, and ulvan -- 9.3.2. Potential applications of selected marine polysaccharides -- 9.3.3. Seaweed-bacteria interactions: a potential factor to improve seaweed-based biorefinery -- 9.4. Associated seaweed bacteria: a potential source of enzymes for hydrolyzing alginate, carrageenan, and ulvan -- 9.4.1. Alginate enzymatic degradation -- 9.4.2. Carrageenan enzymatic degradation -- 9.4.3. Ulvan enzymatic degradation -- 9.5. Processing methods for extraction of monosaccharides from seaweed -- 9.5.1. Seaweed saccharification methods -- 9.5.2. Seaweed monosaccharide applications -- Summary -- Acknowledgments -- References -- Chapter 10: Fermentative production and application of marine microbial exopolysaccharides -- Contents -- 10.1. Introduction -- 10.2. Exopolysaccharides from marine organisms -- 10.2.1. Marine microbial EPS production -- 10.3. Rheological properties of marine exopolysaccharides -- 10.4. Applications of microbial exopolysaccharides -- 10.4.1. Antioxidant properties -- 10.4.2. Anticancer properties -- 10.4.3. Immunomodulatory property -- 10.4.4. Anticoagulant activity and the blood coagulation system -- 10.4.5. Antiviral activity -- 10.4.6. Antilipidemic activity. , 10.4.7. Antibiofilm activity -- 10.4.8. Gelling properties -- 10.4.9. Emulsifying activity -- Concluding remarks -- References -- Section 2: Extraction techniques, structural determination, and methodologies to assess biological activities -- Chapter 11: Marine polysaccharides: extraction techniques, structural determination, and description of their biological activities -- Contents -- 11.1. Introduction -- 11.2. Extraction of marine polysaccharides -- 11.2.1. Agar -- 11.2.2. Carrageenan -- 11.2.3. Laminarin -- 11.2.4. Alginate -- 11.2.5. Ulvan -- 11.2.6. Chitin and chitosan -- 11.2.7. Fucoidan -- 11.2.8. Porphyran -- 11.3. Assessment of intrinsic purity and structural elucidation -- 11.3.1. Methods used in assessing intrinsic purity -- 11.3.2. Structural elucidation -- 11.3.3. Structural characterization-specific polysaccharide -- 11.4. Biological activities -- 11.4.1. Antiviral activities -- 11.4.2. Antibacterial activities -- 11.4.3. Antifungal activities -- 11.4.4. Anticoagulant and antithrombotic activities -- 11.4.5. Antiproliferative, tumor suppressor, apoptotic, and cytotoxicity activities -- 11.4.6. Anti-inflammatory and immunomodulatory activities -- 11.4.7. Antilipidemic (hypocholesterolemic and hypotriglyceridemic), hypoglycemic, and hypotensive activities -- 11.4.8. Antioxidant activity -- Conclusion -- References -- Chapter 12: Fucoidan: a tool for molecular diagnosis and targeted therapy of cardiovascular diseases -- Contents -- 12.1. Introduction -- 12.2. A brief overview of atherosclerosis -- 12.3. Medical imaging of cardiovascular diseases: reality and challenges -- 12.4. Fucoidan and P-selectin: toward a biospecific contrast agent for CVD imaging -- 12.4.1. P-selectin -- 12.4.2. Fucoidan: origin and structure -- 12.4.3. Biological activities of fucoidan -- 12.4.4. P-selectin/fucoidan interaction. , 12.4.5. A fucoidan-based contrast agent for vascular imaging.
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  • 3
    Online Resource
    Online Resource
    Cham : Springer
    Keywords: Life sciences ; Life Sciences ; Microbiology ; Microbial genetics ; Microbial genomics ; Environmental engineering ; Biotechnology ; Environmental engineering ; Marine biotechnology
    Description / Table of Contents: This book serves as essential reading for research scientists and biotechnologists from both academia and industry working in marine biotechnology and related disciplines. The book discusses recent advances and challenges in terms of science, technology, innovation, and policy for the development of the field; and how marine biotechnology may provide new solutions to some of the grand challenges faced by our society. Written in an accessible language, the book is also recommended as a reference text for decision-makers in government and non-governmental organizations in their efforts to foster the development of a global blue economy. With less than 5 % of the vast and rich marine environment explored, our seas and oceans represent a virtually unexplored resource for the discovery of novel product, processes, and development of bio-inspired synthetic drugs with biotechnological potential. As such, the marine environment has been considered Earth's last frontier of exploration. Recent advances in molecular techniques are providing the necessary tools to access on a larger scale the still-untapped ocean resources and, consequently, unveil the promise of the blue biotechnology. Governments are recognizing the potential of marine biotechnology to provide solutions to some of the Grand Challenges of the 21st Century such as sustainable energy and food sources, identification of novel drugs for improved health treatments, and providing new industrial materials and processes. For this reason, advances in marine biotechnology may foster the much-needed source of innovation and economic growth in many countries, and pave the way towards the development of a global blue economy, i.e. a new economic model based on the sustainable exploration of our ocean ecosystems
    Type of Medium: Online Resource
    Pages: Online-Ressource (XX, 616 p, online resource)
    ISBN: 9783319690759
    Series Statement: Grand Challenges in Biology and Biotechnology
    Language: English
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  • 4
    ISSN: 1432-072X
    Keywords: Eubacteria ; Evolution ; Extreme thermophile ; Thermotoga
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Three new strains of eubacterial hyperthermophiles were isolated from continental solfataric springs at Lac Abbé (Djibouti, Africa). Due to their morphology, lipids, and RNA polymerases they belong to the genus Thermotoga. Strains LA4 and LA10 are closely related to Thermotoga neapolitana found up to now only in the marine environment. Strain LA 3 differs from Thermotoga maritima and Thermotoga neapolitana in significant physiological and molecular properties. It is described as the new species Thermotoga thermarum.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 1432-072X
    Keywords: Methanopyrus ; Methanogens ; Archaea ; Hyperthermophilic ; Marine ; Vents
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A novel group of hyperthermophilic rod-shaped motile methanogens was isolated from a hydrothermally heated deep sea sediment (Guaymas Basin, Gulf of California) and from a shallow marine hydrothermal system (Kolbeinsey ridge, Iceland). The grew between 84 and 110°C (opt: 98°C) and from 0.2% to 4% NaCl (opt. 2%) and pH 5.5 to 7 (opt: 6.5). The isolates were obligate chemolithoautotrophes using H2/CO2 as energy and carbon sources. In the presence of sulfur, H2S was formed and cells tended to lyse. The cell wall consisted of a new type of pseudomurein containing ornithin in addition to lysine and no N-acetylglucosamine. The pseudomurein layer was covered by a detergent-sensitive protein surface layer. The core lipid consisted exclusively of phytanyl diether. The GC content of the DNA was 60 mol%. By 16S rRNA comparisons the new organisms were not related to any of the three methanogenic lineages. Based on the physiological and molecular properties of the new isolates, we describe here a new genus, which we name Methanopyrus (the “methane fire”). The type species is Methanopyrus kandleri (type strain: AV19; DSM 6324).
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1573-6776
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 7
    ISSN: 1573-6776
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary A comparison of different systems for the β-glycosidase-atalyzed synthesis of 3,4′-dihydroxypropiophenone 3-O-β-D-glucoside is reported including various enzymatic sources and different reaction conditions. The best yield was obtained using thermophilic β-glycosidase from Sulfolobus solfataricus.
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1573-6776
    Source: Springer Online Journal Archives 1860-2000
    Topics: Process Engineering, Biotechnology, Nutrition Technology
    Notes: Summary Crude homogenate of thermophilic archaebacteriumSulfolobus solfataricus, possessing a β-glycosidase, has been used to synthesize different alkyl β-D-glycosides starting from phenyl β-D-glucoside, phenyl β-D-galactoside and lactose as carbohydrate donors. High product yield (95% with respect to the carbohydrate donor) of octyl β-D-glucoside has been obtained in a two-phase system containing 5% of water. The enantioselection for the galactosyl transfer to the secondary hydroxyl group of propane-1,2-diol is higher than that found using β-galactosidase fromE. coli.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Biotechnology and Bioengineering 35 (1990), S. 559-564 
    ISSN: 0006-3592
    Keywords: Chemistry ; Biochemistry and Biotechnology
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: The method of resting cells has been of interest in the development of biocatalysts applied to organic reactions.This article deals with the use of resting cells of a thermophilic archaebacterium Sulfolobus solfataricus, in the asymmetric reduction of acyclic, cyclic, and aromatic ketones. The system allows the continuous regeneration of endogenous coenzyme with the coupled substrate approach. The results indicate that the direction of hydride attack was equatorial on the re face of the carbonyl group of substrates producing (S)-alcohols with a good optical yield. A convenient system for the reuse of resting cells has been set out to synthesize (S)-alcohols on a preparative scale.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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