Yeast As Biotechnological Tool in Food Industry

Total Page:16

File Type:pdf, Size:1020Kb

Yeast As Biotechnological Tool in Food Industry Open Access Journal of Pharmaceutical Research ISSN: 2574-7797 MEDWIN PUBLISHERS Committed to Create Value for Researchers Yeast as Biotechnological Tool in Food Industry El-Ghwas DE1, Elkhateeb WA1*, Akram M2 and Daba GM1 Review Article 1Chemistry of Natural and Microbial Products Department, Pharmaceutical Industries Volume 5 Issue 3 Division, National Research Centre, Egypt Received Date: July 05, 2021 2Department of Eastern Medicine Government College University Faisalabad-Pakistan, Published Date: July 26, 2021 Pakistan DOI: 10.23880/oajpr-16000243 *Corresponding author: Waill A Elkhateeb, Chemistry of Natural and Microbial Products Department, Pharmaceutical Industries Division, National Research Centre, Dokki, Giza, 12622, Egypt, Tel: +201013241936; Fax: +20233370931; Email: [email protected] Abstract Yeasts are widely spread in nature. Fermentation of sugars by yeast is the oldest and largest application of this technology. Many types of yeasts are used for making many foods: baker’s yeast in bread production, brewer’s yeast in beer fermentation, and yeast in wine. This work describes the prevalence of yeasts in food products. Keywords: Yeast; Food processing; Industrial application; Sugar fermentation Introduction bakeries and breweries [7]. Yeasts are eukaryotic, single-celled microorganisms Yeasts are very common in the environment, and are often isolated from sugar-rich materials. Examples include yeast originated hundreds of millions of years ago, and at naturally occurring yeasts on the skins of fruits and berries leastclassified 1,500 as speciesmembers are ofcurrently the fungus recognized kingdom. [1-3]. The Theyfirst (such as grapes, apples, or peaches), and exudates from are estimated to constitute 1% of all described fungal plants (such as plant saps or cacti). Some yeast is found species [4]. Yeast sizes vary greatly, depending on species in association with soil and insects [8,9]. The ecological and environment, typically measuring 3–4 µm in diameter, function and biodiversity of yeasts are relatively unknown although some yeast can grow to 40 µm in size [5]. Most compared to those of other microorganisms [10]. Yeasts, yeasts reproduce asexually by mitosis, and many do so by the including Candida albicans, Rhodotorula rubra, Torulopsis asymmetric division process known as budding. With their and Trichosporon cutaneum, have been found living in single-celled growth habit, yeasts can be contrasted with molds, which grow hyphae. Fungal species that can take both forms (depending on temperature or other conditions) are andbetween even people’sdeep-sea toesenvironments as part of hosttheir an skin array flora of yeastsYeasts [11- are called dimorphic fungi. 14].also present in the gut flora of mammals and some insects The word “yeast” comes from Old English gist, gyst, and Even if bacteria represent the most studied targets in from the Indo-European root yes-, meaning “boil”, “foam”, or Food Microbiology (pathogens, starter cultures, probiotics, “bubble”[6]. Yeast microbes are probably one of the earliest domesticated organisms. Archaeologists digging in Egyptian date of birth of Food Microbiology as science is the mid of ruins found early grinding stones and baking chambers for 19thproduction century, of whenharmful Pasteur or positive studied compounds), alcoholic fermentation, the official yeast-raised bread, as well as drawings of 4,000-year-old a process executed by yeasts. Also, the useful physiological Yeast as Biotechnological Tool in Food Industry Pharm Res 2 Open Access Journal of Pharmaceutical Research secondary products. It is a complex process and yeasts are biotechnology. Many types of yeasts are used for making responsible for this conversion [25]. Fast fermentation manyproperties foods: of baker’syeast haveyeast led in tobread their production, use in the brewer’s field of of grape juice sugars to high ethanol concentrations is yeast in beer fermentation, and yeast in wine fermentation essential for wine yeasts. Wine yeasts should exhibit and for xylitol production [15]. Also, in industry, yeasts are uniform dispersion and produce minimal foam. At the end commercially used in the production of alcoholic beverages, of the fermentation, sediment should be quickly taken industrial alcohols, baker’s yeast, enzymes and yeast-derived from the wine. It is also important that the yeast should not give slow, sluggish or stuck fermentations [26]. Yeasts role in the spoilage of foods and beverages and some can beflavour pathogenic. products Of [16]. the Furthermore,yeasts, Saccharomyces yeasts play cerevisiae detrimental and related species are widely used in the food and beverage suchalso makeas esters, positive acids, contributions alcohols, aldehydes, to wine ketones, flavour polyols,by the industries. Many species of Saccharomyces are safe (GRAS) volatilesynthesis sulphur of other compounds minor metabolites which directly that define impact the the flavour, wine and the term “yeast” is generally employed as synonymous with Saccharomyces cerevisiae [17]. Therefore, this chapter Kloeckera spp. and Candida spp., dominate at the beginning offlavour the fermentation[27,28]. The andnon-Saccharomyces affect the characteristics yeasts, commonly of wine processing. [29]. The other isolated yeasts are Metschnikowia, Dekkera, will briefly discuss the beneficial aspects of yeasts in food Pichia, Kluyveromyces, Issatchenkia, Saccharomycodes, Baker’s Yeast Zygosaccharomyces, Torulaspora, Debaryomyces, and Schizosaccharomyces [29]. The characteristics of wine yeasts Baker’s yeast, Saccharomyces cerevisiae, is used for must include some properties such as rapid initiation of bakery and confectionary processes throughout the world [18]. Baker’s yeast can be found in different forms tolerance, high osmotolerance, moderate biomass, high like compressed, granular, cream, dried pellet, instant, geneticfermentation, stability, high high sulphitefermentation tolerance, effiiency, low sulphite high bindingethanol encapsulated or frozen [19]. One of the most desirable activity, low foam formation, compacts sediment, resistance characteristics of baker’s yeast strains is high fermentation to desiccation, killer activity, genetic marking, proteolytic rate because is priority desired for baker’s yeast strains since activity and low nitrogen demand. All these properties are it is completely connected to dough-leavening. Yeasts at the found in Saccharomyces cerevisiae [30]. same time encourage gluten network and generate aromatic compounds [20]. Also, rapidly utilization of maltose, tolerance Meat Fermented Food to high levels of sucrose, enduring freeze-thawing stress and resulting in production of high levels of CO2 therefore rising Yeasts are found on meat and processed meat products. dough volume. CO2 is soluble in water and saturates the They have also positive effects on fermented meat products aqueous phase. After reaching saturation, all CO2 produced and many yeast species such as Candida, Debaryomyces, passes through unsaturated gas phase and permit rising of Pichia, Trichosporon, Cryptococcus, Rhodotorula and Yarrowia the volume of bread. Solubilization of CO2 in water results have been isolated from fermented meat products, especially in decreasing the pH and elevates the acidity of the dough sausages [31,32]. Lipolytic and proteolytic activities, which [21]. In addition, CO2 affects rheological characteristics of fermented dough also producing aroma compounds [20,22]. those yeasts were described [33]. Most frequently isolated Aroma compounds are formed widely in the crumb of bread yeastscontribute are toYarrowia flavour lipolyticadue to the and production Debaryomyces of volatiles, hansenii of and the most abundant compounds are alcohols, aldehydes [34]. Debaryomyces hansenii is also used as commercial as well as 2,3-butanedione (diacetyl), 3-hydroxy-2-butanone starter culture in fermented meat products due to its positive (acetoin) and esters [23]. Another desired feature of baker’s yeast is using disaccharide melibiose. Baker’s yeast should be osmotolerant, able to tolerate chemicals (salt, propionates), contributionsDiary Fermented on final product Food [33]. maintain a high growth capacity, should not aggregate and must have a good storage capability. In addition, during the Yeasts such as Candidam lusitaniae, Candida krusei, Kluveromyces lactis, Debaryomyces hansenii, Yarrowia, dough making, the yeast must have a high rate of vitality [24]. lipolytica, Kluyveromyces marxianus, Saccharomyces drying process and after the addition of dry yeast to flour for cerevisiae, Galactomyces geotrichum, Candida zeylanoides and Wine’s Yeast various Pichia species play essential role due to their important functions in dairy-based products such as contributing to the Yeasts are important microorganisms in wine ripening of cheese, speeding up the maturation, improving microbiology. Saccharomyces able to make biotransformation texture and aroma characteristics of certain milk products, of grape sugars into ethanol, carbon dioxide and several increasing pH of cheese, manufacturing of some metabolites Elkhateeb WA, et al. Yeast as Biotechnological Tool in Food Industry. Pharm Res 2021, 5(3): 000243. Copyright© Elkhateeb WA, et al. 3 Open Access Journal of Pharmaceutical Research like ethanol, acetaldehyde, CO2, amino acids and vitamins, nowadays used for some specialty beers. Traditional ciders removing toxic end-products of metabolism, taking part in are produced from spontaneous fermentation of juice some interactions
Recommended publications
  • University of California Riverside
    UNIVERSITY OF CALIFORNIA RIVERSIDE Natamycin, a New Postharvest Biofungicide: Toxicity to Major Decay Fungi, Efficacy, and Optimized Usage Strategies A Dissertation submitted in partial satisfaction of the requirements for the degree of Doctor of Philosophy in Plant Pathology by Daniel Sungen Chen September 2020 Dissertation Committee: Dr. James E. Adaskaveg, Chairperson Dr. Michael E. Stanghellini Dr. Alexander I. Putman Copyright by Daniel Sungen Chen 2020 The Dissertation of Daniel Sungen Chen is approved: Committee Chairperson University of California, Riverside AKNOWLEDGEMENTS Foremost, I thank my mentor Dr. James E. Adaskaveg for accepting me into his research program and teaching me the intricacies of the field of postharvest plant pathology and preparing me for a bright career ahead. His knowledge of the field is unmatched. A special thanks goes out to Dr. Helga Förster, whose expertise and attention to detail has helped me out tremendously in my research and writings. I thank my dissertation committee members, Dr. Michael Stanghellini and Dr. Alexander Putman, for their time spent reviewing my dissertation and their guidance during the pursuit of my doctoral degree. Special thanks also go out to my lab members Dr. Rodger Belisle, Dr. Wei Hao, Dr. Kevin Nguyen, and Nathan Riley for their companionship and much appreciated help with my projects. I would also like to thank my former laboratory members, Dr. Stacey Swanson and Dr. Morgan Thai for their guidance and help during the early years of my graduate program. Thanks go out to Dr. Lingling Hou, Dr. Yong Luo, and Doug Cary for their assistance with performing experimental packingline studies at the Kearney Agricultural Research and Extension Center.
    [Show full text]
  • Molecular Taxonomy of Galactomyces Spp. and Dipodascus Capitatus
    International Journal Of Medical Science And Clinical Inventions Volume 2 issue 12 2015 page no. 1485-1489 e-ISSN: 2348-991X p-ISSN: 2454-9576 Available Online At: http://valleyinternational.net/index.php/our-jou/ijmsci Molecular Taxonomy Of Galactomyces Spp. And Dipodascus Capitatus Associate With Dairy Based On Rdna Sequence Analysis In Iraq Zaidan Khlaif Imran* and Aya Kareem Jabbar Biology Department, All Women College of Science, Babylon University, Hilla, Iraq *Corresponded author: Zaidan Khlaif Imran E.mail:[email protected] ;[email protected] Abstract: Galactomyces spp is a telomorph of Geotrichum candidum (anamorph name). is used as a culture for cheese making and in some traditional fermented milks, few studies have assessed the genetic diversity of Galactomyces spp that exist in traditional cheese making facilities. The aim of this study isolation and molecular taxonomically treated of Galactomyces spp and other Candida spp. correlated with dairy products. The results showed that most dairy samples companioned with two species of Galactomyces: G.candidum and G.geotrichum , D. capitatus and four species of Candida spp.: Candida krusei , C. kefyr, C. utilis and C.glabrata .A total of 23 fungal isolates were diagnosed based on universal primers ITS1 / ITS4 to amplify the Internal transcribed region spacer. Four doubtful G.candidum isolates showed unique sizes of products PCR ranged between 380-400 bp. other Candida PCR product ranged 420-780bp. Sequence analysis identified a doubtful G.candidum into G. candidum and G.geotrichum with 97% similarities and with D. capitatus showed 93% similarities, few intraspecific variation were observed at 312-380bp in the amplicons from the primer pair ITS1-ITS4 commonly are from 380 to 400 bp for G.
    [Show full text]
  • Bio-Removal of Methylene Blue from Aqueous Solution by Galactomyces Geotrichum KL20A
    water Article Bio-Removal of Methylene Blue from Aqueous Solution by Galactomyces geotrichum KL20A Margarita Contreras 1, Carlos David Grande-Tovar 1,* , William Vallejo 1 and Clemencia Chaves-López 2 1 Grupo de Fotoquímica y Fotobiología, Universidad del Atlántico, Puerto Colombia 81007, Colombia; [email protected] (M.C.); [email protected] (W.V.) 2 Faculty of Bioscience and Technology for Food, Agriculture and Environment, University of Teramo, Via R. Balzarini 1, 64100 Teramo, Italy; [email protected] * Correspondence: [email protected]; Tel.: +57-5-3599484 Received: 23 October 2018; Accepted: 7 January 2019; Published: 6 February 2019 Abstract: The conventional treatments used to remove dyes produced as a result of different industrial activities are not completely effective. At times, some toxic by-products are generated, affecting aquatic ecosystems. In this article, an efficient use of microorganisms is presented as a biodegradation technique that is a safe environmental alternative for the benefit of aquatic life. A strain of the yeast Galactomyces geotrichum KL20A isolated from Kumis (a Colombian natural fermented milk) was used for Methylene Blue (MB) bioremoval. Two parameters of the bioremediation process were studied at three different levels: initial dye concentration and growth temperature. The maximum time of MB exposure to the yeast was 48 h. Finally, a pseudo-first-order model was used to simulate the kinetics of the process. The removal percentages of MB, by action of G. geotrichum KL20A were greater than 70% under the best operating conditions and in addition, the kinetic simulation of the experimental results indicated that the constant rate of the process was 2.2 × 10-2 h−1 with a half time for biotransformation of 31.2 h.
    [Show full text]
  • Understanding and Measuring the Shelf-Life of Food Related Titles from Woodhead's Food Science, Technology and Nutrition List
    Understanding and measuring the shelf-life of food Related titles from Woodhead's food science, technology and nutrition list: The stability and shelf-life of food (ISBN 1 85573 500 8) The stability and shelf-life of a food product are critical to its success in the market place, yet companies experience considerable difficulties in defining and understanding the factors that influence stability over a desired storage period. This book is the most comprehensive guide to understanding and controlling the factors that determine the shelf-life of food products. Taints and off-flavours in foods (ISBN 1 85573 449 4) Taints and off-flavours are a major problem for the food industry. Part I of this important collection reviews the major causes of taints and off-flavours, from oxidative rancidity and microbiologically-derived off-flavours, to packaging materials as a source of taints. The second part of the book discusses the range of techniques for detecting taints and off-flavours, from sensory analysis to instrumental techniques, including the development of new rapid on-line sensors. Colour in food ± Improving quality (ISBN 1 85573 590 3) The colour of a food is central to consumer perceptions of quality. This important new collection reviews key issues in controlling colour quality in food, from the chemistry of colour in food to measurement issues, improving natural colour and the use of colourings to improve colour quality. Details of these books and a complete list of Woodhead's food science, technology and nutrition titles can be obtained by: · visiting our web site at www.woodhead-publishing.com · contacting Customer Services (email: [email protected]; fax: +44 (0) 1223 893694; tel.: +44 (0) 1223 891358 ext.
    [Show full text]
  • A New Species of Galactomyces and First Reports of Four Fungi on Wheat Roots in the United Kingdom
    ©Verlag Ferdinand Berger & Söhne Ges.m.b.H., Horn, Austria, download unter www.biologiezentrum.at A new species of Galactomyces and first reports of four fungi on wheat roots in the United Kingdom H. KwasÂna1 & G. L. Bateman2 1 Department of Forest Pathology, Agricultural University, ul. Wojska Polskiego 71c, 60-625, Poznan , Poland 2 Department of Plant Pathology and Microbiology, Rothamsted Research, Harpenden, Hertfordshire, AL5 2JQ, UK KwasÂna H. & Bateman G. (2007) A new species of Galactomyces and first reports of four fungi on wheat roots in the United Kingdom. Sydowia 60 (1): 69±92. A new species, Galactomyces britannicum (IMI395371, MycoBank 511261), is described from the roots of wheat in the UK. Dendryphion penicillatum var. sclerotiale, Fusariella indica, Pseudogymnoascus appendiculatus and Volucrispora graminea are reported for the first time from roots, rhizosphere or stem bases of wheat in the UK. A microconidiogenus synanamorph is described for V. graminea and the species is epitypified to reflect this amendment. Keywords: Dendryphion penicillatum var. sclerotiale, Fusariella indica, Galactomyces britannicum, Pseudogymnoascus appendiculatus, taxonomy, Volu- crispora graminea. The introduction of synthetic low nutrient agar (SNA; Nirenberg 1976) to induce fungal sporulation in Fusarium has proved invalu- able for the assessment of fungal diversity on or in the roots and stem bases of cereal plants (Bateman & KwasÂna 1999, Dawson & Bateman 2001a, b). The medium stimulates a fungal sporulation and allows the isolation of slow-growing species. Isolation studies on SNA have led to the recovery of new speciesof fungiand fungipre- viously unknown from cereal crops. This paper describes one new species and reports four rare spe- cies isolated from the roots, rhizosphere, or stem bases at soil level, of wheat grown in the UK.
    [Show full text]
  • A Novel Function of Galactomyces Candidum in Highly Efficient Ammonia Nitrogen
    bioRxiv preprint doi: https://doi.org/10.1101/397687; this version posted August 22, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. 1 A novel function of Galactomyces candidum in highly efficient ammonia nitrogen 2 removal from low C:N wastewater 3 4 Li Xiaochao1†, Liu Hui2†, Zeng Guihua, Li Hualin2†,Chen Zhinan, Liu Wenbin1*†, 5 Yang Liping2*† 6 7 1College of Life Sciences, Hunan Normal University, Changsha, Hunan 410004, 8 China. 9 2Department of Environmental Science, Changsha Environmental Protection College, 10 Changsha, Hunan 410004, China. 11 12 *For correspondence: Liu Wenbin; Yang Liping 13 †Contributed equally 14 15 16 17 18 19 20 21 22 bioRxiv preprint doi: https://doi.org/10.1101/397687; this version posted August 22, 2018. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-ND 4.0 International license. 23 24 Abstract 25 26 A strain of bacteria that demonstrated efficient nitrogen removal potential under low 27 C:N conditions was screened from landfill leachate. The strain was identified as 28 Galactomyces candidum by ITS sequencing, and growth density and removal of 29 ammonia nitrogen were assessed after 24 h of incubation. The results showed that the 30 optimum ammonia nitrogen reduction conditions for G.
    [Show full text]
  • 7.5 X 11.5.Doubleline.P65
    Cambridge University Press 978-0-521-01483-0 - Introduction to Fungi, Third Edition John Webster and Roland Weber Table of Contents More information Contents Preface to the first edition page xiii Preface to the second edition xv Preface to the third edition xvii Acknowledgements xix Chapter 1 Introduction 1 1.1 What are fungi? 1 1.2 Physiology of the growing hypha 3 1.3 Hyphal aggregates 14 1.4 Spores of fungi 22 1.5 Taxonomy of fungi 32 Chapter 2 Protozoa: Myxomycota (slime moulds) 40 2.1 Introduction 40 2.2 Acrasiomycetes: acrasid cellular slime moulds 40 2.3 Dictyosteliomycetes: dictyostelid slime moulds 41 2.4 Protosteliomycetes: protostelid plasmodial slime moulds 45 2.5 Myxomycetes: true (plasmodial) slime moulds 47 Chapter 3 Protozoa: Plasmodiophoromycota 54 3.1 Introduction 54 3.2 Plasmodiophorales 54 3.3 Control of diseases caused by Plasmodiophorales 62 3.4 Haptoglossa (Haptoglossales) 64 Chapter 4 Straminipila: minor fungal phyla 67 4.1 Introduction 67 4.2 The straminipilous flagellum 68 4.3 Hyphochytriomycota 70 4.4 Labyrinthulomycota 71 Chapter 5 Straminipila: Oomycota 75 5.1 Introduction 75 5.2 Saprolegniales 79 5.3 Pythiales 95 5.4 Peronosporales 115 5.5 Sclerosporaceae 125 © Cambridge University Press www.cambridge.org Cambridge University Press 978-0-521-01483-0 - Introduction to Fungi, Third Edition John Webster and Roland Weber Table of Contents More information viii CONTENTS Chapter 6 Chytridiomycota 127 6.1 Introduction 127 6.2 Chytridiales 134 6.3 Spizellomycetales 145 6.4 Neocallimastigales (rumen fungi) 150 6.5
    [Show full text]
  • Medical and Veterinary Mycology Maximum Performance Solutions Customisable MIC of Bacteria,Mycobacteriaandyeasts,Ensuringaccuratefirsttimeresults
    OFFICIALOFFICIAL JOURNAL JOURNAL OF OF THE THE AUSTRALIAN AUSTRALIAN SOCIETY SOCIETY FOR FOR MICROBIOLOGY MICROBIOLOGY INC. INCINC. VolumeVolume 3636 NumberNumber 22 MayMay 20152015 Medical and veterinary mycology customisable MIC solutions Sensititre provides the only fully customizable system (ARIS 2X, SWIN, OptiRead, AIM, Vizion) with a choice of completely automated, semi-automated, or manual equipment to cover all diagnostic testing needs in the clinical laboratory.More than 240 antimicrobials are available for susceptibility testing of bacteria, mycobacteria and yeasts, ensuring accurate first time results. maximum performance • To find out more visit www.trekds.com or call 1300-735-292 YeastOne™ plates Colorimetric alamarBlue™ agent provides reliable and consistent endpoint determination, with visual read option for yeast and filamentous fungi* *CE/IVD-marked. For research use only in the U.S. Not for use in diagnostic procedures. © 2015 Thermo Fisher Scientific Inc. All rights reserved. © 2015 Thermo Fisher Scientific Inc. All rights The Australian Society for Microbiology Inc. OFFICIAL JOURNAL OF THE AUSTRALIAN SOCIETY FOR MICROBIOLOGY INC. 9/397 Smith Street Fitzroy, Vic. 3065 Tel: 1300 656 423 Volume 36 Number 2 May 2015 Fax: 03 9329 1777 Email: [email protected] www.theasm.org.au Contents ABN 24 065 463 274 Guest For Microbiology Australia Editorial 42 correspondence, see address below. Medical and veterinary mycology 42 Editorial team Wieland Meyer, Laszlo Irinyi and Tania Sorrell Prof. Ian Macreadie, Mrs Jo Macreadie In Focus 44 and Mrs Hayley Macreadie DNA barcoding of human and animal pathogenic fungi: Editorial Board the ISHAM-ITS database 44 Dr Chris Burke (Chair) Dr Gary Lum Prof.
    [Show full text]
  • The 100 Years of the Fungus Collection Mucl 1894-1994
    THE 100 YEARS OF THE FUNGUS COLLECTION MUCL 1894-1994 Fungal Taxonomy and Tropical Mycology: Quo vadis ? Taxonomy and Nomenclature of the Fungi Grégoire L. Hennebert Catholic University of Louvain, Belgium Notice of the editor This document is now published as an archive It is available on www.Mycotaxon.com It is also produced on CD and in few paperback copies G. L. Hennebert ed. Published by Mycotaxon, Ltd. Ithaca, New York, USA December 2010 ISBN 978-0-930845-18-6 (www pdf version) ISBN 978-0-930845-17-9 (paperback version) DOI 10.5248/2010MUCL.pdf 1894-1994 MUCL Centenary CONTENTS Lists of participants 8 Forword John Webser 13 PLENARY SESSION The 100 Year Fungus Culture Collection MUCL, June 29th, 1994 G.L. Hennebert, UCL Mycothèque de l'Université Catholique de Louvain (MUCL) 17 D. Hawksworth, IMI, U.K. Fungal genetic resource collections and biodiversity. 27 D. van der Mei, CBS, MINE, Netherlands The fungus culture collections in Europe. 34 J. De Brabandere, BCCM, Belgium The Belgian Coordinated Collections of Microorganisms. 40 Fungal Taxonomy and tropical Mycology G.L. Hennebert, UCL Introduction. Fungal taxonomy and tropical mycology: Quo vadis ? 41 C.P. Kurtzman, NRRL, USA Molecular taxonomy in the yeast fungi: present and future. 42 M. Blackwell, Louisiana State University, USA Phylogeny of filamentous fungi deduced from analysis of molecular characters: present and future. 52 J. Rammeloo, National Botanical Garden, Belgium Importance of morphological and anatomical characters in fungal taxonomy. 57 M.F. Roquebert, Natural History Museum, France Possible progress of modern morphological analysis in fungal taxonomy. 63 A.J.
    [Show full text]
  • Public Release of Subsurface Management Plan
    Oregon Caves National Monument Subsurface Management Plan 1 TABLE OF CONTENTS I. INTRODUCTION A. Purpose and Significance........................................................................................ 4 B. Legislative and Administrative Requirements......................................................... 5 II. PRESENT RESOURCE STATUS............................................................................. 7 III. DATA COLLECTION A. Cave Classification………………………………………………………………... 12 B. Inventories…………………………………………………………………………. 12 IV. RESOURCE PROTECTION A. Visitor Use 1. Carrying Capacity……………………………………….……………………….12 2. Caving Permits…………………………………………………………………. 13 B. Interpretation 1. Publications............................................................................................ 15 2. Interpretive Tours................................................................................... 16 3. Outreach Programs................................................................................ 16 4. Audio-visual.......................................................................................... 16 5. Visitor Survey....................................................................................... 16 C. Ranger Patrols.......................................................................................................... 17 D. Cave Locations.................................. E. Gates......................................................................................................................... 18 F. Cave Alteration........................................................................................................
    [Show full text]
  • Diversity and Distribution of Hidden Cultivable Fungi Associated with Marine Animals of Antarctica Fungal Biology
    Fungal Biology 123 (2019) 507e516 Contents lists available at ScienceDirect Fungal Biology journal homepage: www.elsevier.com/locate/funbio Diversity and distribution of hidden cultivable fungi associated with marine animals of Antarctica Valeria Martins Godinho a, Maria Theresa Rafaela de Paula a, Debora Amorim Saraiva Silva a, Karla Paresque b, Aline Paternostro Martins c, * Pio Colepicolo c, Carlos Augusto Rosa a, Luiz Henrique Rosa a, a Departamento de Microbiologia, Instituto de Ci^encias Biologicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil b Laboratorio de Bentologia, Universidade Federal de Alagoas, Maceio, AL, Brazil c Departamento de Bioquímica, Instituto de Química, Universidade de Sao~ Paulo, Sao~ Paulo, Brazil article info abstract Article history: In the present study, we surveyed the distribution and diversity of fungal assemblages associated with 10 Received 22 November 2018 species of marine animals from Antarctica. The collections yielded 83 taxa from 27 distinct genera, which Received in revised form were identified using molecular biology methods. The most abundant taxa were Cladosporium sp. 1, 17 April 2019 Debaryomyces hansenii, Glaciozyma martinii, Metschnikowia australis, Pseudogymnoascus destructans, Accepted 1 May 2019 Thelebolus cf. globosus, Pseudogymnoascus pannorum, Tolypocladium tundrense, Metschnikowia australis, Available online 14 May 2019 and different Penicillium species. The diversity, richness, and dominance of fungal assemblages ranged Corresponding Editor: Nik Money among the host; however, in general, the fungal community, which was composed of endemic and cold- adapted cosmopolitan taxa distributed across the different sites of Antarctic Peninsula, displayed high Keywords: diversity, richness, and dominance indices. Our results contribute to knowledge about fungal diversity in Antarctic ocean the marine environment across the Antarctic Peninsula and their phylogenetic relationships with species Extremophiles that occur in other cold, temperate, and tropical regions of the World.
    [Show full text]
  • YEAST Dynamics During the Natural Fermentation Process of Table Olives (Negrinha De Freixo Cv.)
    Food Microbiology 46 (2015) 582e586 Contents lists available at ScienceDirect Food Microbiology journal homepage: www.elsevier.com/locate/fm YEAST dynamics during the natural fermentation process of table olives (Negrinha de Freixo cv.) * ** Ermelinda L. Pereira , Elsa Ramalhosa, Ana Borges, Jose A. Pereira, Paula Baptista Mountain Research Center (CIMO), Polytechnic Institute of Bragança, School of Agriculture, Campus Sta. Apolonia, Apartado 1172, 5301-855 Bragança, Portugal article info abstract Article history: Yeast population and dynamics associated to spontaneous fermentation of green table olives Negrinha de Received 30 July 2014 Freixo cv. were evaluated. Olives and brine samples were taken at different fermentation times, and yeast Received in revised form were enumerated by standard plate count and identified by sequencing of the internal transcribed spacer 30 September 2014 (ITS) region of the nuclear ribosomal DNA (rDNA). Saccharomyces cerevisiae was the most frequent, Accepted 11 October 2014 followed by Candida tropicalis, Pichia membranifaciens and Candida boidini, representing together 94.8% of Available online 19 October 2014 the total isolates. Galactomyces reessii was also identified for the first time in table olives. The highest species diversity was found between 44 and 54 days of fermentation, both in brine and olive pulp. Keywords: Yeasts Furthermore, high similarity was observed between brine and olive pulp microbiotas. In conclusion, Brine these results give valuable information to table olive industrials in order to achieve more knowledge on Olive pulp the fermentation process of this important Protected Designation of Origin product. Diversity © 2014 Elsevier Ltd. All rights reserved. 1. Introduction So far, the production of table olives Negrinha de Freixo PDO has been conducted in an empirical way without knowledge Table olives are one of the most important fermented vegetables about the microbiota and the chemical properties occurring over in Portugal.
    [Show full text]