A Functional and Structural Study of Three Bacterial Nucleic Acid
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Metaproteogenomic Insights Beyond Bacterial Response to Naphthalene
ORIGINAL ARTICLE ISME Journal – Original article Metaproteogenomic insights beyond bacterial response to 5 naphthalene exposure and bio-stimulation María-Eugenia Guazzaroni, Florian-Alexander Herbst, Iván Lores, Javier Tamames, Ana Isabel Peláez, Nieves López-Cortés, María Alcaide, Mercedes V. del Pozo, José María Vieites, Martin von Bergen, José Luis R. Gallego, Rafael Bargiela, Arantxa López-López, Dietmar H. Pieper, Ramón Rosselló-Móra, Jesús Sánchez, Jana Seifert and Manuel Ferrer 10 Supporting Online Material includes Text (Supporting Materials and Methods) Tables S1 to S9 Figures S1 to S7 1 SUPPORTING TEXT Supporting Materials and Methods Soil characterisation Soil pH was measured in a suspension of soil and water (1:2.5) with a glass electrode, and 5 electrical conductivity was measured in the same extract (diluted 1:5). Primary soil characteristics were determined using standard techniques, such as dichromate oxidation (organic matter content), the Kjeldahl method (nitrogen content), the Olsen method (phosphorus content) and a Bernard calcimeter (carbonate content). The Bouyoucos Densimetry method was used to establish textural data. Exchangeable cations (Ca, Mg, K and 10 Na) extracted with 1 M NH 4Cl and exchangeable aluminium extracted with 1 M KCl were determined using atomic absorption/emission spectrophotometry with an AA200 PerkinElmer analyser. The effective cation exchange capacity (ECEC) was calculated as the sum of the values of the last two measurements (sum of the exchangeable cations and the exchangeable Al). Analyses were performed immediately after sampling. 15 Hydrocarbon analysis Extraction (5 g of sample N and Nbs) was performed with dichloromethane:acetone (1:1) using a Soxtherm extraction apparatus (Gerhardt GmbH & Co. -
Achromobacter Buckle Infection Diagnosed by a 16S Rdna Clone
Hotta et al. BMC Ophthalmology 2014, 14:142 http://www.biomedcentral.com/1471-2415/14/142 CASE REPORT Open Access Achromobacter buckle infection diagnosed by a 16S rDNA clone library analysis: a case report Fumika Hotta1†, Hiroshi Eguchi1*, Takeshi Naito1†, Yoshinori Mitamura1†, Kohei Kusujima2† and Tomomi Kuwahara3† Abstract Background: In clinical settings, bacterial infections are usually diagnosed by isolation of colonies after laboratory cultivation followed by species identification with biochemical tests. However, biochemical tests result in misidentification due to similar phenotypes of closely related species. In such cases, 16S rDNA sequence analysis is useful. Herein, we report the first case of an Achromobacter-associated buckle infection that was diagnosed by 16S rDNA sequence analysis. This report highlights the significance of Achromobacter spp. in device-related ophthalmic infections. Case presentation: A 56-year-old woman, who had received buckling surgery using a silicone solid tire for retinal detachment eighteen years prior to this study, presented purulent eye discharge and conjunctival hyperemia in her right eye. Buckle infection was suspected and the buckle material was removed. Isolates from cultures of preoperative discharge and from deposits on the operatively removed buckle material were initially identified as Alcaligenes and Corynebacterium species. However, sequence analysis of a 16S rDNA clone library using the DNA extracted from the deposits on the buckle material demonstrated that all of the 16S rDNA sequences most closely matched those of Achromobacter spp. We concluded that the initial misdiagnosis of this case as an Alcaligenes buckle infection was due to the unreliability of the biochemical test in discriminating Achromobacter and Alcaligenes species due to their close taxonomic positions and similar phenotypes. -
Gut Microbiome Alterations in Ulcerative Colitis and After Moxibustion Intervention
Gut Microbiome Alterations In Ulcerative Colitis And After Moxibustion Intervention Qin Qi Shanghai University of Traditional Chinese Medicine Ya-Nan Liu Shanghai University of Traditional Chinese Medicine Si-Yi Lv Shanghai University of Traditional Chinese Medicine Huan-Gan Wu Shanghai University of Traditional Chinese Medicine Lin-Shuang Zhang Zhejiang Institute for Food and Drug Control Zhan Cao Tongji University School of Medicine Hui-Rong Liu Shanghai University of Traditional Chinese Medicine Xiao-Mei Wang ( [email protected] ) Shanghai University of Traditional Chinese Medicine Lu-Yi Wu Shanghai University of Traditional Chinese Medicine Research Article Keywords: Ulcerative colitis, Moxibustion, Gut microbiota, Metagenomic Posted Date: August 11th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-789670/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/22 Abstract Background: Recent studies have shown that the pathogenesis of ulcerative colitis (UC) is closely related to the gut microbiota. Moxibustion, a common treatment in traditional Chinese medicine, is the burning of the herb moxa over acupuncture points. Moxibustion has been used to improve the inammation and gastrointestinal dysfunctions in gastrointestinal disorders such as UC. In this study, we investigated whether moxibustion could improve the gut microbial dysbiosis induced by dextran sulphate sodium (DSS). Methods: Twenty-ve male rats were randomly assigned into ve groups: normal (NG), UC model (UC), moxibustion (UC+MOX), mesalazine (UC+MES), and normal rats with moxibustion (NG+MOX). The UC rat model was established by administering DSS solution. The rats in the UC+MOX and NG+MOX groups were treated with moxibustion at Tianshu (bilateral, ST25) points once daily for 7 consecutive days, and the UC+MES group rats were treated with mesalazine once daily for 7 consecutive days. -
Achromobacter Infections and Treatment Options
AAC Accepted Manuscript Posted Online 17 August 2020 Antimicrob. Agents Chemother. doi:10.1128/AAC.01025-20 Copyright © 2020 American Society for Microbiology. All Rights Reserved. 1 Achromobacter Infections and Treatment Options 2 Burcu Isler 1 2,3 3 Timothy J. Kidd Downloaded from 4 Adam G. Stewart 1,4 5 Patrick Harris 1,2 6 1,4 David L. Paterson http://aac.asm.org/ 7 1. University of Queensland, Faculty of Medicine, UQ Center for Clinical Research, 8 Brisbane, Australia 9 2. Central Microbiology, Pathology Queensland, Royal Brisbane and Women’s Hospital, 10 Brisbane, Australia on August 18, 2020 at University of Queensland 11 3. University of Queensland, Faculty of Science, School of Chemistry and Molecular 12 Biosciences, Brisbane, Australia 13 4. Infectious Diseases Unit, Royal Brisbane and Women’s Hospital, Brisbane, Australia 14 15 Editorial correspondence can be sent to: 16 Professor David Paterson 17 Director 18 UQ Center for Clinical Research 19 Faculty of Medicine 20 The University of Queensland 1 21 Level 8, Building 71/918, UQCCR, RBWH Campus 22 Herston QLD 4029 AUSTRALIA 23 T: +61 7 3346 5500 Downloaded from 24 F: +61 7 3346 5509 25 E: [email protected] 26 http://aac.asm.org/ 27 28 29 on August 18, 2020 at University of Queensland 30 31 32 33 34 35 36 37 38 39 2 40 Abstract 41 Achromobacter is a genus of non-fermenting Gram negative bacteria under order 42 Burkholderiales. Although primarily isolated from respiratory tract of people with cystic Downloaded from 43 fibrosis, Achromobacter spp. can cause a broad range of infections in hosts with other 44 underlying conditions. -
Genome-Wide Investigation of Cellular Functions for Trna Nucleus
Genome-wide Investigation of Cellular Functions for tRNA Nucleus- Cytoplasm Trafficking in the Yeast Saccharomyces cerevisiae DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Hui-Yi Chu Graduate Program in Molecular, Cellular and Developmental Biology The Ohio State University 2012 Dissertation Committee: Anita K. Hopper, Advisor Stephen Osmani Kurt Fredrick Jane Jackman Copyright by Hui-Yi Chu 2012 Abstract In eukaryotic cells tRNAs are transcribed in the nucleus and exported to the cytoplasm for their essential role in protein synthesis. This export event was thought to be unidirectional. Surprisingly, several lines of evidence showed that mature cytoplasmic tRNAs shuttle between nucleus and cytoplasm and their distribution is nutrient-dependent. This newly discovered tRNA retrograde process is conserved from yeast to vertebrates. Although how exactly the tRNA nuclear-cytoplasmic trafficking is regulated is still under investigation, previous studies identified several transporters involved in tRNA subcellular dynamics. At least three members of the β-importin family function in tRNA nuclear-cytoplasmic intracellular movement: (1) Los1 functions in both the tRNA primary export and re-export processes; (2) Mtr10, directly or indirectly, is responsible for the constitutive retrograde import of cytoplasmic tRNA to the nucleus; (3) Msn5 functions solely in the re-export process. In this thesis I focus on the physiological role(s) of the tRNA nuclear retrograde pathway. One possibility is that nuclear accumulation of cytoplasmic tRNA serves to modulate translation of particular transcripts. To test this hypothesis, I compared expression profiles from non-translating mRNAs and polyribosome-bound translating mRNAs collected from msn5Δ and mtr10Δ mutants and wild-type cells, in fed or acute amino acid starvation conditions. -
FUNCTIONAL and MECHANISTIC CHARACTERIZATION of TWO TRNA MODIFYING ENZYMES LAURA CAROLE KEFFER-WILKES Master of Science, Universi
FUNCTIONAL AND MECHANISTIC CHARACTERIZATION OF TWO TRNA MODIFYING ENZYMES LAURA CAROLE KEFFER-WILKES Master of Science, University of Lethbridge, 2012 A Thesis Submitted to the School of Graduate Studies Of the University of Lethbridge In Partial Fulfillment of the Requirements for the Degree DOCTOR OF PHILOSOPHY Department of Chemistry and Biochemistry University of Lethbridge LETHBRIDGE, ALBERTA, CANADA © Laura Keffer-Wilkes, 2016 FUNCTIONAL AND MECHANISTIC CHARACTERIZATION OF TWO TRNA MODIFYING ENZYMES LAURA CAROLE KEFFER-WILKES Date of Defence: June 28, 2016 Dr. Ute Wieden-Kothe Associate Professor Ph.D. Supervisor Dr. Tony Russell Assistant Professor Ph.D. Thesis Examination Committee Member Dr. Stacey Wetmore Professor Ph.D. Thesis Examination Committee Member Dr. Hans-Joachim Wieden Professor Ph.D. Thesis Examination Committee Member Dr. Eugene Mueller Professor Ph.D. External Examiner University of Louisville Louisville, Kentucky Dr. Elizabeth Schultz Associate Professor Ph.D. Internal External Examiner University of Lethbridge Dr. Michael Gerken Professor Ph.D. Chair, Thesis Examination Committee Abstract The formation of pseudouridine (Ѱ) and 5-methyluridine (m5U) in the T-arm of transfer RNAs (tRNAs) is near-universally conserved. These two modifications are formed in Escherichia coli by the pseudouridine synthase TruB and the S-adenosylmethionine- dependent methyltransferase TrmA, respectively. In this thesis, I investigate the function and mechanisms of these two tRNA modifying enzymes. First, in vitro and in vivo analysis of TruB reveals that this enzyme is acting as a tRNA chaperone which proves a long outstanding hypothesis. Secondly, characterization of ligand binding by TrmA shows that binding is cooperative and disruption of tRNA elbow region tertiary interactions by TrmA is essential for efficient tRNA binding and catalysis, leading to future analysis. -
A Protein Subunit of Human Rnase P, Rpp14, and Its Interacting Partner, OIP2, Have 335 Exoribonuclease Activity
A protein subunit of human RNase P, Rpp14, and its interacting partner, OIP2, have 335 exoribonuclease activity Taijiao Jiang and Sidney Altman* Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, CT 06520 Contributed by Sidney Altman, February 12, 2002 -The processing of precursor tRNAs at their 5 and 3 termini is a presence of [␣-32P]UTP. Internally labeled SupS1-3Ј was pre fundamental event in the biosynthesis of tRNA. RNase P is gener- pared from internally labeled 5Ј-SupS1-3Ј by removing the 5Ј ally responsible for endonucleolytic removal of a leader sequence leader sequence by using purified human RNase P. For the of precursor tRNA to generate the mature 5 terminus. However, synthesis of 5Ј-32P-labeled 5Ј-Tyr-3Ј, transcription reactions were much less is known about the RNase P counterparts or other performed with nonlabeled NTPs, the RNA was purified and proteins that are active at the tRNA 3 terminus. Here we show that then was treated with calf intestinal phosphatase, extracted two one of the human RNase P subunits, Rpp14, together with one of times with phenol͞chloroform and one time with chloroform. its interacting protein partners, OIP2, is a 335 exoribonuclease Recovery was by ethanol precipitation. 5Ј-Tyr-3Ј was labeled .with a phosphorolytic activity that processes the 3 terminus of with [␥-32P]ATP by using polynucleotide kinase precursor tRNA. Immunoprecipitates of a crude human RNase P Adult enhancer factor-1 (AEF) RNA, a single-stranded RNA complex can process both ends of precursor tRNA by hydrolysis, from Drosophila melanogaster (12), was labeled as indicated by but purified RNase P has no exonuclease activity. -
B Number Gene Name Strand Orientation Protein Length Mrna
list list sample) short list predicted B number Operon ID Gene name assignment Protein length mRNA present mRNA intensity Gene description Protein detected - Strand orientation Membrane protein detected (total list) detected (long list) membrane sample Proteins detected - detected (short list) # of tryptic peptides # of tryptic peptides # of tryptic peptides # of tryptic peptides # of tryptic peptides Functional category detected (membrane Protein detected - total Protein detected - long b0001 thrL + 21 1344 P 1 0 0 0 0 thr operon leader peptide Metabolism of small molecules 1 b0002 thrA + 820 13624 P 39 P 18 P 18 P 18 P(m) 2 aspartokinase I, homoserine dehydrogenase I Metabolism of small molecules 1 b0003 thrB + 310 6781 P 9 P 3 3 P 3 0 homoserine kinase Metabolism of small molecules 1 b0004 thrC + 428 15039 P 18 P 10 P 11 P 10 0 threonine synthase Metabolism of small molecules 1 b0005 b0005 + 98 432 A 5 0 0 0 0 orf, hypothetical protein Open reading frames 2 b0006 yaaA - 258 1047 P 11 P 1 2 P 1 0 orf, hypothetical protein Open reading frames 3 b0007 yaaJ - 476 342 P 8 0 0 0 0 MP-GenProt-PHD inner membrane transport protein Miscellaneous 4 b0008 talB + 317 20561 P 20 P 13 P 16 P 13 0 transaldolase B Metabolism of small molecules 5 b0009 mog + 195 1296 P 7 0 0 0 0 required for the efficient incorporation of molybdate into molybdoproteins Metabolism of small molecules 6 b0010 yaaH - 188 407 A 2 0 0 0 0 PHD orf, hypothetical protein Open reading frames 7 b0011 b0011 - 237 338 P 13 0 0 0 0 putative oxidoreductase Miscellaneous 8 b0012 htgA -
Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales
Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales TECHNICAL BIOSAFETY COMMITTEE (TBC) NATIONAL CENTER FOR GENETIC ENGINEERING AND BIOTECHNOLOGY (BIOTEC) NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY (NSTDA) MINISTRY OF SCIENCE AND TECHNOLOGY (MOST) 2015 Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales TECHNICAL BIOSAFETY COMMITTEE (TBC) NATIONAL CENTER FOR GENETIC ENGINEERING AND BIOTECHNOLOGY (BIOTEC) NATIONAL SCIENCE AND TECHNOLOGY DEVELOPMENT AGENCY (NSTDA) MINISTRY OF SCIENCE AND TECHNOLOGY (MOST) 2015 Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales Technical Biosafety Committee National Center for Genetic Engineering and Biotechnology National Science and Technology Development Agency (NSTDA) © National Center for Genetic Engineering and Biotechnology 2015 ISBN : 978-616-12-0386-3 Tel : +66(0)2-564-6700 Fax : +66(0)2-564-6703 E-mail : [email protected] URL : http://www.biotec.or.th Printing House : P.A. Living Printing Co.,Ltd 4 Soi Sirintron 7 Road Sirintron District Bangplad Province Bangkok 10700 Tel : +66(0)2-881 9890 Fax : +66(0)2-881 9894 Preface Genetically Modified Microorganisms (GMMs) were first used in B.E. 2525 to produce insulin in industrial medicine. Currently, GMMs are used in various industries, such as the food, pharmaceutical and bioplastic industries, to manufacture a number of important consumer products. To ensure operator and environmental safety, the Technical Biosafety Committee (TBC) of the National Center for Genetic Engineering and Biotechnology (BIOTEC), the National Science and Technology Development Agency (NSTDA), has prepared guidelines for GMM work, publishing “Biosafety Guidelines for Contained Use of Genetically Modified Microorganisms at Pilot and Industrial Scales” in B.E. -
A Possible Functional Link Between RNA Degradation and Transcription in Bacillus Subtilis
A possible functional link between RNA degradation and transcription in Bacillus subtilis Dissertation for the award of the degree “Doctor of Philosophy” Division of Mathematics and Natural Sciences of the Georg-August-University Göttingen within the program “Microbiology and Biochemistry” of the Georg-August University School of Science (GAUSS) submitted by Martin Benda from Prague (Czech Republic) Göttingen 2020 Thesis Committee Prof. Dr. Jörg Stülke (Supervisor and 1st Reviewer) Institute for Microbiology and Genetics, Department of General Microbiology, Georg-August-University Göttingen Prof. Dr. Rolf Daniel (2nd Reviewer) Institute for Microbiology and Genetics, Department of Genomic and Applied Microbiology, Georg-August- University Göttingen Prof. Dr. Fabian M. Commichau Institute for Biotechnology, Department of Synthetic Microbiology, Brandenburg University of Technology Cottbus-Senftenberg Additional members of the Examination Board Prof. Dr. Markus Bohnsack Department of Molecular Biology, University Medical Center Göttingen Prof. Dr. Patrick Cramer Department of Molecular Biology, Max Planck Institute for Biophysical Chemistry, Göttingen Prof. Dr. Stefanie Pöggeler Institute for Microbiology and Genetics, Department of Genetics of Eukaryotic Microorganisms, Georg- August-University Göttingen Date of oral examination: September 17th, 2020 I hereby declare that this Ph.D. thesis entitled “A possible functional link between RNA degradation and transcription in Bacillus subtilis” has been written independently and with no other sources and aids than quoted. Martin Benda Acknowledgements First of all, I would like to express my deep thanks to my supervisor Prof. Dr. Jörg Stülke for the great guidance during this work. He put his full trust in me and gave me the opportunity to work on this intricate, but engaging topic of RNA degradation. -
Contamination of Burn Wounds by Achromobacter
Annals of Burns and Fire Disasters - vol. XXIX - n. 3 - September 2016 CONTAMINATION OF BURN WOUNDS BY ACHROMOBACTER XYLOSOXIDANS FOLLOWED BY SEVERE INFECTION: 10-YEAR ANALYSIS OF A BURN UNIT POPULATION CONTAMINATION DES ZONES BRÛLÉES PAR ACHROMOBACTER XYLOSOXIDANS, ENTRAÎNANT UNE INFECTION SÉVÈRE: ANALYSE SUR 10 ANS * Schulz A., Perbix W., Fuchs P.C., Seyhan H., Schiefer J.L. Department of Plastic Surgery, Hand Surgery, Burn Center, University of Witten/Herdecke, Cologne-Merheim Medical Center (CMMC), Cologne, Germany SUMMARY. Gram-negative infections predominate in burn surgery. Until recently, Achromobacter species were described as sepsis-caus - ing bacteria in immunocompromised patients only. Severe infections associated with Achromobacter species in burn patients have been rarely reported. We retrospectively analyzed all burn patients in our database, who were treated at the Intensive Care Burn Unit (ICBU) of the Cologne Merheim Burn Centre from January 2006 to December 2015, focusing on contamination and infection by Achromobacter species. We identified 20 patients with burns contaminated by Achromobacter species within the 10-year study period. Four of these patients showed signs of infection concomitant with detection of Achromobacter species. Despite receiving complex antibiotic therapy based on antibiogram and resistogram typing, 3 of these patients, who had extensive burns, developed severe sepsis. Two patients ultimately died of multiple organ failure. In 1 case, Achromobacter xylosoxidans was the only isolate detected from the swabs and blood samples taken during the last stage of sepsis. Achromobacter xylosoxidans contamination of wounds of severely burned immunocompromised patients can lead to systemic lethal infection. Close monitoring of burn wounds for contamination by Achromobacter xylosoxidans is essential, and appropriate therapy must be administered as soon as possible. -
Long-Term Phenotypic Evolution of Bacteria
LETTER doi:10.1038/nature13827 Long-term phenotypic evolution of bacteria Germa´n Plata1,2, Christopher S. Henry3 & Dennis Vitkup1,4 For many decades comparative analyses of protein sequences and is sometimes observed within the same species, a transition from high structures have been used to investigate fundamental principles of to low phenotypic similarity occurs primarily at the genus level. molecular evolution1,2. In contrast, relatively little is known about Analyses of phenotypic evolution, such as the morphological varia- the long-term evolution of species’ phenotypic and genetic properties. tion of beaks in Darwin’s finches3, provided the original impetus and This represents an important gap in our understanding of evolu- context for understanding natural selection. Because the evolutionary tion, as exactly these proprieties play key roles in natural selection importance and physiological role of specific phenotypic traits change and adaptation to diverse environments. Here we perform a com- over time, it is often difficult to connect genotype to phenotype to fit- parative analysis of bacterial growth and gene deletion phenotypes ness across long evolutionary distances, especially for metazoan organ- using hundreds of genome-scale metabolic models. Overall, bacte- isms. For microbial species, on the other hand, the ability to metabolize rial phenotypic evolution can be described by a two-stage process different nutrient sources, although clearly not the only important phe- with a rapid initial phenotypic diversification followed by a slow notype, always remains an essential determinant of their fitness and long-term exponential divergence. The observed average divergence lifestyle. Even though a large-scale comparative analysis of microbial trend, with approximately similar fractions of phenotypic properties phenotypes—such as growth on different nutrients or the impact of changing per unit time, continues for billions of years.