The Transcriptional Landscape of the Production Organism Pseudomonas Putida

Total Page:16

File Type:pdf, Size:1020Kb

The Transcriptional Landscape of the Production Organism Pseudomonas Putida Downloaded from orbit.dtu.dk on: Sep 26, 2021 The Transcriptional Landscape of the Production Organism Pseudomonas putida D'Arrigo, Isotta Publication date: 2016 Document Version Publisher's PDF, also known as Version of record Link back to DTU Orbit Citation (APA): D'Arrigo, I. (2016). The Transcriptional Landscape of the Production Organism Pseudomonas putida. Novo Nordisk Foundation Center for Biosustainability. General rights Copyright and moral rights for the publications made accessible in the public portal are retained by the authors and/or other copyright owners and it is a condition of accessing publications that users recognise and abide by the legal requirements associated with these rights. Users may download and print one copy of any publication from the public portal for the purpose of private study or research. You may not further distribute the material or use it for any profit-making activity or commercial gain You may freely distribute the URL identifying the publication in the public portal If you believe that this document breaches copyright please contact us providing details, and we will remove access to the work immediately and investigate your claim. The Transcriptional Landscape of the Production Organism Pseudomonas putida Ph.D. Thesis Isotta D’Arrigo The Novo Nordisk Foundation Center for Biosustainability The Technical University of Denmark April 2016 The Transcriptional Landscape of the Production Organism Pseudomonas putida Ph.D. Thesis 2016 © Isotta D’Arrigo Novo Nordisk Center for Biosustainability Technical University of Denmark Kogle Alle 6, DK - 2970 Hørsholm Denmark Cover art: image adapted by Se Hyeuk Kim. “It’s not what you look at that matters, it’s what you see” (Henry David Thoreau) To my grandfather, I did not know why I am here Preface This thesis is written as a partial fulfillment of the requirements to obtain a Ph.D. degree at the Technical University of Denmark. The work presented here was performed between May 2013 and April 2016 at the Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark. The work was supervised by Katherine S. Long, Associate Professor from the Technical University of Denmark. Funding was provided by The Novo Nordisk Foundation and a Ph.D. grant from the People Programme (Marie Curie Actions) of the European Union’s Seventh Framework Programme, [FP7-People-2012-ITN], under grant agreement no. 317058, “BACTORY”. The thesis was evaluated by Professor Juan Luis Ramos Martin from Abengoa Research, by Jeppe Vinther, Associate Professor at the University of Copenhagen, and by Alex Toftgaard Nielsen, Professor at Technical University of Denmark. Isotta D’Arrigo Hørsholm, April 2016 i Acknowledgements First, I would like to thank my supervisor Katherine S. Long for her continuous support and motivation during my entire Ph.D. You have been an encouraging guide, who let me choose the direction but also drive me on the proper way. Thanks to all the members (and ex-) of the RNA group, I cannot imagine how it would be without you! Special thanks to Holger, for inspiring me so many times and in so many occasions even without being at the center. You have been my first teacher, colleague and friend in the lab. I have learnt how to “bend the rules” thanks to you! Martin, for your generous patience and passion in making my things work. For all those days spent in front of a black screen with weird codes running…people watching me were thinking I was doing difficult programming work…I let them think of it, they did not know I was just trying to learn the “cd” command. A big thanks to Klara; even if you talk a lot, really a lot, now I can honestly say “it has been a big pleasure to work with you!” Together we worked in the RNA lab, together we crashed our “head” with bioinformatics in Český Krumlov, together we crashed my head in Cancun, and together we had also a lot of fun! Beside at work, I am so glad to have a friend like you…thanks a lot for everything! A huge thanks to Michelino, because you are not just a helpful and always happy co-worker but mainly a great boyfriend. Thank you for listening, for understanding me, for your continuous reinforcement. Thanks Miche, for always taking care of me... and for teaching me the proper use of “by chance”. Xiaochen, for all our discussions about work problems and scientific doubts, but at the end let’s order pizza vah! ii I would like to express my thanks to the Bactory people. Thanks to Søren and Mette, who built an amazing program and gave me the opportunity to take part in it. Thanks to all the Bactory Ph.D. students, it was a great pleasure starting with you that 1st of May three years ago, and since then we have always helped and strengthen each other. In particular many thanks to Mimi, for all your microbiology lessons, for your continuous support at work and in daily life, for all the laughs we had from Stockholm to China and for the pleasure of having you “endless” and singing Chandelier. Thanks to papiciulo Henrique, for your incredible help in every situation. You know “Hey brother…if the sky comes falling down for you, There’s nothing in this world I wouldn’t do.” Thanks to Giuggiolina for all our conversations, all our outbursts, and all our relaxing “cenette”. I will miss everything! I would like to thank the Cfb collaborators João, Niko, Markus, Maja, thanks a lot for this final rush, I really appreciated all of your efforts. Thanks to the Cool Office and all the people who make it cool, it was awesome to spend these three years with you (Sofie, Patri, Dario)! I also would like to thank Carlotta who has always stood on my side. Thank you for our long talks, funny moments, and Elvira breaks! Big big thanks to Mr. Kim for all the help in the lab, with the figures, and with any kind of doubts. Always available to help, you are really awesome! Thanks to Laura, Virginia, Roberto, Alicia, Anna, Gigi, Nabin, Christian, Ida, Rosa, Math because all of you guys have helped me to enjoy these three years at Cfb. I would like to thank Allan and Anne from Novozymes, for hosting me in your department. It has been a wonderful experience with you! I also would to thank the Italian group here in Copenhagen. Thanks to my brother Niccolò, who bravely took a decision and started a new adventure here. My historical friends Giulia and Isacco; I am closing iii another circle and I will bring you in the next one. Thanks to Marchino for all the funny moments and Eugene. My flatmate Nicola; it has been great to know you, even if you support Djokovic. I would like to thank my mum, dad, and grandmother Erichina, because even with the distance I have felt your strong support. You have always believed in me and push me to follow my dreams. Thanks a lot for that! Finally, I would like to thank all my friends in Italy and abroad that never give up on me. I cannot mention you all but you are amazing! iv Abstract Bacterial cell factories represent a valid alternative to fossil fuel-based production. A promising bacterium that can be optimized as cell factory is Pseudomonas putida. However, its development in bioproduction applications poses some challenges including a clear understanding of the bacterial system biology. This thesis has the aim of facilitating the development of P. putida KT2440 as a bacterial cell factory by investigating the transcriptome of the bacterium under different conditions (e.g. growth and stress). The main goals are the identification of differentially expressed genes, which provide information on bacterial adaptation to different environments, and the identification of non-coding RNAs, which regulate gene expression. This work focuses on several aspects of P. putida highlighting genomic features such as transcription start sites (TSSs), RNA regulatory elements such as riboswitches and small RNAs (sRNAs), metabolic pathways and transporter systems. The results reported here significantly increase knowledge of the P. putida transcriptome, adaptation mechanisms, and reveal novel bacterial features that will aid the design and optimization of the bacterium as a cell factory. v Dansk resumé Bakterielle cellefabrikker udgør et reelt alternativ til produktion baseret på fossile brændstoffer. En lovende kandidatbakterie, der kan optimeres som cellefabrik, er Pseudomonas putida. Brugen af denne bakterie til bioproduktion har dog nogle udfordringer, hvilket inkluderer forståelsen af det bakterielle system. Denne afhandling har som mål fremme udviklingen af P. putida KT2440 som en bakteriel celle fabrik ved at undersøge transkriptomet af bakterien under forskellige forhold (fx vækst og stress). De overordnende mål er identifikation af differentielt udtrykte gener, hvilket giver information om den bakterielle adaptation til forskellige miljøer, og identifikation af ikke-kodende RNA’er, der regulerer genekspression. Arbejdet fokuserer på adskillige aspekter af P. putida og fremhæver genomiske egenskaber som transkriptionelle startsteder (TSSs), regulatoriske RNA elementer som ’riboswithes’ og små RNA’er (sRNAs), metaboliske netværk og transportsystemer. Resultaterne, der her rapporteres, øger markant forståelsen af P. putidas transkriptom, tilpasningsmekanismer og beskriver bakterielle egenskaber, der vil hjælpe med designet og optimeringen af denne bakterielle cellefabrik. vi Publications Included in this thesis I. D’Arrigo, K. Bojanovič, X. Yang, M. H. Rau, K. S. Long. (2016). Genome-wide mapping of transcription start sites yields novel insights into the primary transcriptome of Pseudomonas putida. Environmental Microbiology. Manuscript in press. K. Bojanovič, I. D’Arrigo, K. S. Long. (2016). Global transcriptional responses to oxidative, osmotic, and imipenem stress conditions in Pseudomonas putida. Manuscript in preparation.
Recommended publications
  • Applications of Biotechnology
    Applications of Biotechnology Superbug, edible vaccine,hgh,humulin By-Dhriti Ghose Assistant Professor UG and PG Dept Of Botany Raja Narendra Lal Khan Women’s College(Autonomous) Role of transgenics in Bioremediation(Superbug) Bioremediation-(Definition and introduction)The use of either naturally occuring or deliberately introduced microorganisms to consume and break down environmental pollutants, in order to clean a polluted site. Nature has its own way of cleaning the environment by removing xenobiotics(xenobiotics are chemicals found in the environment which are not produced by the organisms.These are mostly produced by human activities and excite public awareness due to their ability to interact with the living environment.)to maintain a perfect balance. but in this era of industrialization the rate of xenobiotics discharges has crossed the tolerance limit of the nature. Therefore, there is a need to find out the method of remediating xenobiotics from the environment. Microbial remediation of xenobiotics has proved the effectiveness and low cost technology but there are several limitations in using microbes. Thus, genetic engineering approaches are used by genetic engineers to construct new strains of microbes (Genetically engineered microorganisms, GEMs or transgenic microorganisms) that have the unique characteristics compared to the wild type and broad spectrum of catabolic potential for bioremediation of xenobiotics. Oil spill occurs due release of petroleum hydrocarbons of any form into the environment due to human activity. The spill can originate from oil tankers,off shore platforms,oil rigs etc. The effect of this on marine ecosystem is terrifying. Prof. Ananda mohan chakraborty et al. (1970) developed and patented a “superbug” that was made to degrade oil and hence can clean up this oil spillover from the sea.
    [Show full text]
  • Stress-Related Pseudomonas Genes Involved in Production Of
    FEMS Microbiology Letters 244 (2005) 243–250 www.fems-microbiology.org Stress-related Pseudomonas genes involved in production of bacteriocin LlpA Downloaded from https://academic.oup.com/femsle/article/244/2/243/470295 by guest on 30 September 2021 Paulina Estrada de los Santos 1, Annabel H.A. Parret 1,2, Rene´ De Mot * Centre of Microbial and Plant Genetics, Faculty of Applied Bioscience and Engineering, Katholieke Universiteit Leuven, Kasteelpark Arenberg 20, B 3001 Heverlee Leuven, Belgium Received 14 December 2004; received in revised form 27 January 2005; accepted 27 January 2005 First published online 4 February 2005 Edited by Y. Oken Abstract Pseudomonas sp. BW11M1 produces a novel type of bacteriocin that inhibits the growth of Pseudomonas putida GR12-2R3 and some phytopathogenic fluorescent Pseudomonas. A collection of mutants was screened for altered bacteriocin production pheno- types. Strongly reduced bacteriocin production was found to be caused by inactivation of the recA gene or the spoT gene. Con- versely, in a recJ mutant, the bacteriocin was constitutively overproduced. The same phenotype was observed for a mutant hit in a gene of unknown function. The predicted gene product belongs to a distinct subgroup of prokaryotic helicase-like proteins within the SWI/SNF family of regulatory proteins. One mutant that also exhibited a bacteriocin overproducer phenotype was defi- cient in the production of the peptidoglycan-associated lipoprotein OprL. This study shows that various environmental stress response pathways are involved in controlling expression of the Pseudomonas sp. BW11M1 bacteriocin. Ó 2005 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved.
    [Show full text]
  • Biological Control of Watermelon Seedling Blight Caused By
    Vol. 54, 2018, No. 3: 138–146 Plant Protect. Sci. https://doi.org/10.17221/168/2016-PPS Biological Control of Watermelon Seedling Blight Caused by Acidovorax citrulli Using Antagonistic Bacteria from the Genera Curtobacterium, Microbacterium and Pseudomonas Sumer HORUZ 1,2* and Yesim Aysan 1 1Plant Protection Department, Faculty of Agriculture, Cukurova University, Adana, Turkey; 2Plant Protection Department, Faculty of Agriculture, Erciyes University, Kayseri, Turkey *Corresponding author: [email protected] Abstract Horuz S., Aysan Y. (2018): Biological control of watermelon seedling blight caused by Acidovorax citrulli using antagonistic bacteria from the genera Curtobacterium, Microbacterium and Pseudomonas. Plant Protect. Sci., 54: 138–146. The biological control of the watermelon seedling blight and fruit blotch disease was investigated by screening the potential use of antagonistic bacteria. Between May and August 2012, totally 322 putative antagonistic bacteria were isolated from symptomless melon and watermelon plants grown in Adana, Hatay, and Osmaniye provinces of the Eastern Mediterranean Region of Turkey. In vitro dual culture tests showed that 54 out of 322 strains inhibited the Acidovorax citrulli (Ac) growth with an appearance of clear zones between 2.3 and 27.0 mm in diameter. However, the remaining 268 strains did not exhibit any antagonistic activity against Ac. Seed treatments with fourteen individual antagonistic bacteria resulted in a significant reduction in disease incidence (DI) and severity (DS) ranging between 14.06–79.47% and between 4.57–41.49%, respectively. The bacteria Pseudomonas oryzihabitans (Antg-12), Micro- bacterium oxydans (Antg-57), Curtobacterium flaccumfaciens (Antg-198), and Pseudomonas fluorescens (Antg-273) were the most potent antagonistic bacterial isolates which reduced DI and DS as compared to the untreated control.
    [Show full text]
  • Mycorrhiza-Induced Resistance: More Than the Sum of Its Parts?
    Opinion Mycorrhiza-induced resistance: more than the sum of its parts? 1 2 3 1 Duncan D. Cameron , Andrew L. Neal , Saskia C.M. van Wees , and Jurriaan Ton 1 Department of Animal and Plant Sciences, University of Sheffield, Western Bank, Sheffield, S10 2TN, UK 2 Centre for Sustainable Soils and Grassland Systems, Rothamsted Research, Harpenden, AL5 2JQ, UK 3 Plant–Microbe Interactions, Department of Biology, Utrecht University, P.O. Box 800.56, 3508 TB Utrecht, The Netherlands Plants can develop an enhanced defensive capacity in growth-promoting rhizobacteria (PGPR) that possess the response to infection by arbuscular mycorrhizal fungi capacity to enhance plant growth and suppress pests and (AMF). This ‘mycorrhiza-induced resistance’ (MIR) pro- diseases. Some of these mycorrhizosphere-inhabiting bac- vides systemic protection against a wide range of attack- teria can act as ‘mycorrhiza-helper bacteria’ and promote ers and shares characteristics with systemic acquired the efficiency of mycorrhizal symbiosis [6] (Box 1). As a resistance (SAR) after pathogen infection and induced consequence of these interactions, it has been suggested systemic resistance (ISR) following root colonisation by that the benefits of AMF on whole-plant physiology are at non-pathogenic rhizobacteria. It is commonly assumed least partially determined by biological activities in the that fungal stimulation of the plant immune system is mycorrhizosphere [6–8]. solely responsible for MIR. In this opinion article, we AMF can suppress plant pests and diseases through present a novel model of MIR that integrates different induction of systemic resistance [9–11]. Nutrient supply aspects of the induced resistance phenomenon. We experiments have revealed that MIR cannot be attributed propose that MIR is a cumulative effect of direct plant to improved nutritional status [12].
    [Show full text]
  • Characterisation of Pseudomonas Spp. Isolated from Foods
    07.QXD 9-03-2007 15:08 Pagina 39 Annals of Microbiology, 57 (1) 39-47 (2007) Characterisation of Pseudomonas spp. isolated from foods Laura FRANZETTI*, Mauro SCARPELLINI Dipartimento di Scienze e Tecnologie Alimentari e Microbiologiche, sezione Microbiologia Agraria Alimentare Ecologica, Università degli Studi di Milano, Via Celoria 2, 20133 Milano, Italy Received 30 June 2006 / Accepted 27 December 2006 Abstract - Putative Pseudomonas spp. (102 isolates) from different foods were first characterised by API 20NE and then tested for some enzymatic activities (lipase and lecithinase production, starch hydrolysis and proteolytic activity). However subsequent molecular tests did not always confirm the results obtained, thus highlighting the limits of API 20NE. Instead RFLP ITS1 and the sequencing of 16S rRNA gene grouped the isolates into 6 clusters: Pseudomonas fluorescens (cluster I), Pseudomonas fragi (cluster II and V) Pseudomonas migulae (cluster III), Pseudomonas aeruginosa (cluster IV) and Pseudomonas chicorii (cluster VI). The pectinolytic activity was typical of species isolated from vegetable products, especially Pseudomonas fluorescens. Instead Pseudomonas fragi, predominantly isolated from meat was characterised by proteolytic and lipolytic activities. Key words: Pseudomonas fluorescens, enzymatic activity, ITS1. INTRODUCTION the most frequently found species, however the species dis- tribution within the food ecosystem remains relatively The genus Pseudomonas is the most heterogeneous and unknown (Arnaut-Rollier et al., 1999). The principal micro- ecologically significant group of known bacteria, and bial population of many vegetables in the field consists of includes Gram-negative motile aerobic rods that are wide- species of the genus Pseudomonas, especially the fluores- spread throughout nature and characterised by elevated cent forms.
    [Show full text]
  • Pseudomonas Putida Strain B2017 Produced As Technical Grade Active Ingredient Controls Fungal and Bacterial Crop Diseases
    Biocontrol Science and Technology ISSN: 0958-3157 (Print) 1360-0478 (Online) Journal homepage: https://www.tandfonline.com/loi/cbst20 Pseudomonas putida strain B2017 produced as technical grade active ingredient controls fungal and bacterial crop diseases Clara Oliver, Iker Hernández, Marta Caminal, José M. Lara & Carolina Fernàndez To cite this article: Clara Oliver, Iker Hernández, Marta Caminal, José M. Lara & Carolina Fernàndez (2019): Pseudomonasputida strain B2017 produced as technical grade active ingredient controls fungal and bacterial crop diseases, Biocontrol Science and Technology To link to this article: https://doi.org/10.1080/09583157.2019.1645304 View supplementary material Published online: 18 Jul 2019. Submit your article to this journal View Crossmark data Full Terms & Conditions of access and use can be found at https://www.tandfonline.com/action/journalInformation?journalCode=cbst20 BIOCONTROL SCIENCE AND TECHNOLOGY https://doi.org/10.1080/09583157.2019.1645304 Pseudomonas putida strain B2017 produced as technical grade active ingredient controls fungal and bacterial crop diseases Clara Oliver, Iker Hernández , Marta Caminal, José M. Lara and Carolina Fernàndez Futureco Bioscience S.A., Barcelona, Spain ABSTRACT ARTICLE HISTORY Biological control is emerging as a feasible alternative to chemical Received 1 March 2019 pesticides for the protection of crop plants. Pseudomonas putida Accepted 15 July 2019 shows enormous potential as biological control agent (BCA) not KEYWORDS only because it is well reported to control a number of relevant Biological control; crop crop diseases, but also because it has a short generation time, diseases; Pseudomonas colonises plants and their environment, exerts its BCA activity putida B2017; technical grade through a range of different mechanisms, and promotes plant active ingredient; scale-up growth.
    [Show full text]
  • Emendation of Pseudomonas Straminea Iizuka and Komagata 1963
    International Journal of Systematic and Evolutionary Microbiology (2000), 50, 1513–1519 Printed in Great Britain Emendation of Pseudomonas straminea Iizuka NOTE and Komagata 1963 Masataka Uchino,1 Yoshimasa Kosako,2 Tai Uchimura1 and Kazuo Komagata1 Author for correspondence: Tai Uchimura. Tel: j81 3 5477 2327. Fax: j81 3 3427 6435. e-mail: tai!nodai.ac.jp 1 Department of Applied The description of Pseudomonas straminae Iizuka and Komagata 1963 was Biology and Chemistry, emended with data newly obtained. The spelling of the name of this taxon is Faculty of Applied Bioscience, Tokyo also corrected as Pseudomonas straminea. Strains that were previously named University of Agriculture, ‘Pseudomonas ochracea’ were identified as P. straminea. Sakuragaoka 1-1-1, Setagaya-ku, Tokyo 156-8502, Japan Keywords: Pseudomonas straminea, Pseudomonas straminae, Pseudomonas 2 Japan Collection of Microorganisms, The Institute of Physical and Chemical Research (RIKEN), Wako-shi, Saitama 351-0198, Japan During the study of the microflora of rice, Iizuka & Recently, Behrendt et al. (1999) reported the isolation Komagata (1963c, d, e) isolated large numbers of of yellow-pigmented bacteria from the phyllosphere of Pseudomonas strains from unhulled rice and rough grasses and identified them as Pseudomonas graminis. rice. Pseudomonas straminea was isolated from The distribution of these Pseudomonas species that Japanese paddies and was characterized by the pro- produce water-insoluble yellow pigments is rather duction of a water-insoluble yellow pigment and a limited to plant materials, and their pathogenicity has water-soluble greenish-yellow pigment (Iizuka & not been reported (Iizuka & Komagata, 1963c; Komagata, 1963e). This species was validated and the Hildebrand et al., 1994; Behrendt et al., 1999).
    [Show full text]
  • First Case of Human Infection Due to Pseudomonas Fulva, An
    JOURNAL OF CLINICAL MICROBIOLOGY, Feb. 2010, p. 660–664 Vol. 48, No. 2 0095-1137/10/$12.00 doi:10.1128/JCM.01849-09 Copyright © 2010, American Society for Microbiology. All Rights Reserved. First Case of Human Infection Due to Pseudomonas fulva,an Environmental Bacterium Isolated from Cerebrospinal Fluidᰔ Marisa N. Almuzara,1* Miryam Vazquez,2 Naoto Tanaka,3 Marisa Turco,2 Maria S. Ramirez,4 Eduardo L. Lopez,2 Fernando Pasteran,5 Melina Rapoport,5 Adriana Procopio,2 and Carlos A. Vay1 Laboratorio de Bacteriología, Instituto de Fisiopatología y Bioquímica Clínica, Hospital de Clínicas Jose´ de San Martín, Facultad de Farmacia y Bioquímica, Universidad de Buenos Aires, Ciudad Auto´noma de Buenos Aires, Argentina1; Laboratorio de Bacteriología y Servicio de Infectología, Hospital de Nin˜os Ricardo Gutierrez, Ciudad Auto´noma de Buenos Aires, Argentina2; NODAI Culture Collection, Tokyo University of Agriculture, Tokyo, Japan3; Departamento de Microbiología, Inmunología y Parasitología, Facultad de Medicina, Universidad de Buenos Aires, Ciudad Auto´noma de Buenos Aires, Argentina4; and Servicio Antimicrobianos, Departamento de Bacteriología, Instituto Nacional de Enfermedades Infecciosas—ANLIS Carlos G. Malbra´n, Ciudad Auto´noma de Buenos Aires, Argentina5 Received 19 September 2009/Returned for modification 30 October 2009/Accepted 10 December 2009 We report the first case of human infection due to Pseudomonas fulva. P. fulva caused acute meningitis following the placement of a drainage system in a 2-year-old female. Additionally, the isolate displayed a VIM-2 carbapenemase in a class 1 integron context. CASE REPORT carried out; however, the CSF culture obtained by lumbar puncture (for bacteria, fungi, and mycobacteria) was negative.
    [Show full text]
  • Transcriptome Changes in Pseudomonas Putida KT2440 During Medium-Chain-Length Polyhydroxyalkanoate Synthesis Induced by Nitrogen Limitation
    International Journal of Molecular Sciences Article Transcriptome Changes in Pseudomonas putida KT2440 during Medium-Chain-Length Polyhydroxyalkanoate Synthesis Induced by Nitrogen Limitation Dorota Dabrowska 1, Justyna Mozejko-Ciesielska 2 , Tomasz Pokój 1 and Slawomir Ciesielski 1,* 1 Department of Environmental Biotechnology, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn, Poland; [email protected] (D.D.); [email protected] (T.P.) 2 Department of Microbiology and Mycology, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn, Poland; [email protected] * Correspondence: [email protected]; Tel.: +48-89-5234162 Abstract: Pseudomonas putida’s versatility and metabolic flexibility make it an ideal biotechnological platform for producing valuable chemicals, such as medium-chain-length polyhydroxyalkanoates (mcl-PHAs), which are considered the next generation bioplastics. This bacterium responds to environmental stimuli by rearranging its metabolism to improve its fitness and increase its chances of survival in harsh environments. Mcl-PHAs play an important role in central metabolism, serving as a reservoir of carbon and energy. Due to the complexity of mcl-PHAs’ metabolism, the manner in which P. putida changes its transcriptome to favor mcl-PHA synthesis in response to environmental stimuli remains unclear. Therefore, our objective was to investigate how the P. putida KT2440 wild type and mutants adjust their transcriptomes to synthesize mcl-PHAs in response to nitrogen limitation when supplied with sodium gluconate as an external carbon source. We found that, under nitrogen limitation, mcl-PHA accumulation is significantly lower in the mutant deficient in the stringent response than in the wild type or the rpoN mutant.
    [Show full text]
  • Gammaproteobacteria Constituents
    Thompson DK and Wickham GS, Adv Microb Res 2: 002 DOI: 10.24966/AMR-694X/100002 HSOA Journal of Advances in Microbiology Research Research Article high metal resistance of Gammaproteobacteria constituents. Gammaproteobacteria and Keywords: Bacterial phylogenetics; Chromium stress; Small-sub- unit ribosomal RNA gene clone technology; Soil microbial commu- Firmicutes are Resistant to nities Long-Term Chromium Expo- Introduction Hexavalent chromium [Cr(VI)], in the form of chromate (CrO 2-) sure in Soil 4 2- or dichromate (Cr2O7 ), is a widely distributed anthropogenic pollut- Dorothea K Thompson1* and Gene S Wickham2 ant in terrestrial ecosystems due to its prevalent use as a strong oxidiz- ing agent in various industrial processes and military defense appli- 1Department of Pharmaceutical Sciences, Campbell University, Buies Creek, North Carolina, USA cations [1,2]. Environmental chromium (Cr) persists predominantly in one of two chemically stable oxidation states, the trivalent form 2 Department of Biological Sciences, Purdue University, West Lafayette, [Cr(III)] or the hexavalent form [Cr(VI)] [3]. Oxyanion chromate is Indiana, USA mobile in soils and sediments due to its high water solubility [3,4]. Moreover, Cr(VI) is highly toxic to all living organisms, with chronic exposures leading to such detrimental health impacts as mutagenesis Abstract and carcinogenesis [5-7]. The adverse biological effect of chromate is The impact of long-term chromium contamination on the struc- attributable to its transport across cellular membranes via surface an- ture of soil microbial communities under relevant field conditions re- ion transport systems [4,8,9]. Chromate toxicity is associated with the mains inadequately documented, despite the prevalent deposition generation of Reactive Oxygen Species (ROS) during the intracellular of toxic chromate in both terrestrial and aquatic ecosystems due to partial reduction of Cr(VI) to the unstable intermediate Cr(V), a high- anthropogenic activities.
    [Show full text]
  • Identification of Pseudomonas Species and Other Non-Glucose Fermenters
    UK Standards for Microbiology Investigations Identification of Pseudomonas species and other Non- Glucose Fermenters Issued by the Standards Unit, Microbiology Services, PHE Bacteriology – Identification | ID 17 | Issue no: 3 | Issue date: 13.04.15 | Page: 1 of 41 © Crown copyright 2015 Identification of Pseudomonas species and other Non-Glucose Fermenters Acknowledgments UK Standards for Microbiology Investigations (SMIs) are developed under the auspices of Public Health England (PHE) working in partnership with the National Health Service (NHS), Public Health Wales and with the professional organisations whose logos are displayed below and listed on the website https://www.gov.uk/uk- standards-for-microbiology-investigations-smi-quality-and-consistency-in-clinical- laboratories. SMIs are developed, reviewed and revised by various working groups which are overseen by a steering committee (see https://www.gov.uk/government/groups/standards-for-microbiology-investigations- steering-committee). The contributions of many individuals in clinical, specialist and reference laboratories who have provided information and comments during the development of this document are acknowledged. We are grateful to the Medical Editors for editing the medical content. For further information please contact us at: Standards Unit Microbiology Services Public Health England 61 Colindale Avenue London NW9 5EQ E-mail: [email protected] Website: https://www.gov.uk/uk-standards-for-microbiology-investigations-smi-quality- and-consistency-in-clinical-laboratories
    [Show full text]
  • Morphological Structure of Polystyrene Degradated by Soil Bacteria from Sarimukti Final Landfill Cipatat Bandung
    International Journal of Science and Society, Volume 1, Issue 3, 2019 Morphological Structure of Polystyrene Degradated by Soil Bacteria from Sarimukti Final Landfill Cipatat Bandung Tri Rahayu Hidayat1), Ida Indrawati2), Tati Herlina3) 1,2Departement of Biology, Faculty of Matematics and Natural Sciences, University Padjadjaran 3Departement of Chemistry, Faculty of Matematics and Natural Sciences, University Padjadjaran email: [email protected] Abstract The amount of Styrofoam waste in Bandung reaches 27,02 tons per month. Styrofoam used as packaging food or drinks, that are formed on styrene and benzene. The migration of benzene from packaging materials to food can cause various diseases. The most potent source of finding indigenous bacteria that can degrade of synthetic polymers is in the Final Landfill. This research method uses exploratory methods that are analyzed descriptively consisting of the stages of the biodegradation test with the Winogradsky Column method, calculation of the percentage of weight loss of Styrofoam, physical analysis with Scanning Electron Microscope (SEM). The results of this study found 4 species of polystyrene degrading bacteria is Pseudomonas aeruginosa, Bacillus amyloliquefaciens, Bacillus cereus and Bacillus firmus. The percentage reduction in dry weight of polystyrene showed in the first week the polystyrene weight decreased by 8.27% and increased weight loss up to the eighth week which reached 18.23% and and physical analysis with Scanning Electron Microscope (SEM) indicates that the process of degradation by soil bacteria showed the formation of holes or pores on the surface. These polystyrene degrading bacteria from Sarimukti landfills can be recommended as an environmentally friendly method for reducing styrofoam waste.
    [Show full text]