DOCSLIB.ORG

Journal of Bacteriology

Total Page：16

File Type：pdf, Size：1020Kb

Download full-text PDF Read full-text
Journal of Bacteriology JOURNAL OF BACTERIOLOGY VOLUME 126 * NUMBER 3 * JUNE 1976 EDITORIAL BOARD L. LEON CAMPBELL, Editor-in-Chief (1980) University of Delaware, Newark S. G. BRADLEY, Editor (1979) ALLEN T. PHILLIPS, Editor (1980) Virginia Commonwealth University, Richmond Pennsylvania State University, University Park, Pa. ROY CURTISS HI, Editor (1979) CARL SCHNAITMAN, Editor (1978) University ofAlabama, Birmingham University of Virginia, Charlottesville ELIZABETH McFALL, Editor (1980) H. E. UMBARGER, Editor (1976) New York University, New York, N.Y. Purdue University, Lafayette, Ind. James N. Adams (1976) Walton L. Fangman (1978) Eugene W. Nester (1978) Arthur I. Aronson (1976) Gerald R. Fink (1978) Donald P. Nierlich (1977) Gad Avigad (1977) W. R. Finnerty (1976) Michio Oishi (1977) Stephen D. Barbour (1976) Walter R. Guild (1978) Ronald H. Olsen (1978) Blaine Beaman (1976) George Hegeman (1977) Charles Panos (1978) Claire M. Berg (1976) James A. Hoch (1977) Leo Parks (1976) Richard S. Berk (1977) Joy Hochstadt (1977) Martin Pato (1978) Harriet Bernheimer (1977) Stanley C. Holt (1977) Paul V. Phibbs (1976) Judith S. Bond (1977) Joseph Inselburg (1978) Charles C. Remsen III (1976) Winfried Boos (1976) Sam Kaplan (1977) William S. Reznikoff (1976) Jean Brenchley (1977) Jost Kemper (1978) Palmer Rogers (1978) George H. Brownell (1977) David E. Kenneil (1977) Antonio H. Romano (1976) Richard 0. Burns (1977) Bruce C. Kline (1977) Robert Rownd (1977) Donald B. Clewell (1977) Robert L. Lester (1978) Harold L. Sadoff (1977) Stanley N. Cohen (1976) Hillel S. Levinson (1978) Irwin H. Segel (1976) Ronald S. Cole (1977) James S. Lovett (1977) Jane K. Setlow (1978) S. F. Conti (1978) K. Brooks Low (1976) Stanley K. Shapiro (1976) Stephen Cooper (1978) Calvin S. McLaughlin (1978) Simon Silver (1976) John E. Cronan, Jr. (1977) P. T. Magee (1977) Lucile Smith (1978) Walter J. Dobrogosz (1976) Michael H. Malamy (1978) James A. Wechsler (1978) Patrick R. Dugan (1977) Manley Mandel (1978) David White (1977) Alan D. Elbein (1976) Robert E. Marquis (1976) Clifford A. Woolfolk (1976) Wolfgang Epstein (1978) Neil H. Mendelson (1978) Howard Zalkin (1976) David P. Fan (1978) Gene E. Michaels (1977) Robert A. Day, Managing Editor GiseUa Pollock, Director of Editorial Services Linda Illig, Production Editor 1913 I St., N. W., Washington, D. C. 20006 EX OFFICIO Helen R. Whiteley, President (1975-1976) Harlyn 0. Halvorson, Vice-President (1975-1976) J. Mehsen Joseph, Secretary Brinton M. Miller, Treasurer The Journal ofBacteriology, a publication of the American submitted manuscripts, and general editorial matters should Society for Microbiology. 1913 I St., N.W., Washington, D.C. be directed to the ASM Publications Office, 1913 I St., N.W., 20006, is devoted to the advancement and dissemination of Washington, D.C. 20006 (area 202 833-9680). fundamental knowledge concerning bacteria and other micro- organisms. The Journal is published monthly, and the twelve numbers are divided into four volumes per year. The non- Second class postage paid at Washington, D.C. 20006, and at member subscription price is $90 per year. Single copies are additional mailing offices. $8. The member subscription price is $17 per year. Corre- Made in the United States of America. spondence relating to subscriptions, reprints, defective copies, Copyright © 1976, American Society for Microbiology. availability of back issues, lost or late proofs, disposition of All Rights Reserved. Author Index Adams, James N., 1104 Hacking, Andrew J., 1166 Rake, Adrian V., 1305 Adhya, Sankar, 1108 Hamilton, W. Allan, 1224, 1232 Raymond, Jonathan, 1089 Hancock, Robert E. W., 1347 Rebouche, Charles J., 1207 Bass, Richard, 1119 Harriman, Philip D., 1141 Reeves, Peter, 1052, 1347 Beck, Barbara, 1250 Hebeler, Bruce H., 1180, 1186 Reyes, Oscar, 1108 Bergquist, P. L., 1063 Heffernan, Laurel, 1119, 1132 Rudd, Joanne, 1344 Bird, Robert E., 1215 Hochhauser, Steven J., 1082 Body, Barbara A., 1149 Holden, Joseph A., 1141 Sadaie, Yoshito, 1037 Broquist, Harry P., 1207 Sanemori, Hiroshi, 1030 Brownell, George H.,,1104 Ingebretsen, Ole C., 1075 Sanner, Tore, 1075 Brownstein, Bernard H., 1149 Ives, David H., 1136 Schaeffer, Pierre, 1342 Seto, Hiroyuki, 1113 Caro, Lucien, 1215 Jarvis, Audrey W., 1232 Shapiro, Lucille, 1305 Chandler, Michael, 1215 Shida, Hisatoshi, 1025 Chapman, Ann, 1351 Kadota, Hajime, 1342 Shinozawa, Takao, 1025 Cintr6n, Nitza M., 1082 Kapoor, V., 1245 Silbert, David F., 1351 Cole, Roger M., 1285 Kawasaki, Takashi, 1030 Slater, Martin L., 1339 Collins, Mary Lynne Perille, Kido, Toshiko, 1261 Soda, Kenji, 1261 1316, 1326 Kung, Fang-Chien, 1089 Subrahmanyam, C. S., 1042 Collins, Stephen H., 1224, 1232 Sypherd, Paul S., 1266 Curtiss, Roy, III, 1194 Lampky, J. R., 1278 Lin, E. C. C., 1166 Das, H. K., 1042 Lindsay, Raymond J., 1232 Tabita, F. Robert, 1271 Davies, John K., 1347 Lusk, Joan E., 1096 Tomasz, Alexander, 1113 Davis, Minh-Tam B., 1136 Truman, Penelope, 1063 McFadden, Bruce A., 1271 Egi, Yoshiko, 1030 Mendelson, Neil H., 1285 Uchida, Aritsune, 1342 Eisenberg, Roselyn J., 1344 Mooney, Duane T., 1266 Elchisak, Mary, 1344 Wall, Judy D., 1141 Englesberg, Ellis, 1119 Narui, Kikuko, 1037 Weiss, Bernard, 1082 Newman, E. B., 1245 Weiss, Richard L., 1173 Falkinham, Joseph O., III, 1194 Niederman, Robert A., 1316, White, Brian J., 1082 Foster, Gayle C., 1297 1326 Wilcox, Gary, 1132 Foster, R. Scott 1297 Wilson, David B., 1156 Park, James T., 1250 Wong, Brenda B., 1096 Glaser, Donald A., 1089 Park, Myung Hee, 1096 Wood, Nancy B., 1305 Gottesman, Max, 1108 Pohlman, Timothy, 1351 Potter, R., 1245 Yamamoto, Tatsuo, 1261 Haag, Steven M., 1285 Pugsley, Anthony P., 1052 Young, Frank E., 1180, 1186 INSTRUCTIONS TO AUTHORS Submit manuscripts in duplicate (original and Abstract. An Abstract appears at the beginning of one copy) to ASM Publications Office, 1913 I St., each paper in the Journal. The Abstract should not N.W., Washington, D.C. 20006. exceed 250 words. General policy. Any manuscript submitted must Literature Cited. In the text, references are cited be a report of unpublished original research, which by number. The Literature Cited section should be is not being considered for publication elsewhere. typed in alphabetical order, by first author, and Each manuscript should present the results of numbered. Each reference should include the title of an independent, cohesive study; numbered series the article and inclusive pagination. Names of papers are discouraged. Papers that deal primarily journals are abbreviated according to Bibliographic with a method should not be submitted. Guide for Editors & Authors (American Chemical The "editorial style" of the Journal essentially Society, 1974). Citations of abstracts, theses, "un- follows the CBE Style Manual (3rd ed., AIBS, 1972). published data," "personal communication," and, For bacterial genetic systems, the recommendations "in press" will not be accepted in the Literature of Demerec et al. (Genetics 54:61, 1966) should be Cited. followed, with the limited modifications of Taylor Tables. Each table should be typed on a separate and Trotter, Sanderson, and Low (Bacteriol. Rev. page. The data should be arranged so that columns 36:504-524; 558-586; and 587-607, 1972). For yeast, of like material read down, not across. Explanatory Chlamydomonas, and several fungal species, sym- footnotes are permitted, but detailed descriptions bols such as those given in Handbook of Micro- of the experiments are not. The materials and biology (1974, A. I. Laskin and H. A. Lechevalier, methods used to gain the data should properly eds., CRC Press, Cleveland, p. 665-711, Vol. IV) remain in the section of that name. should be employed. For genetic nomenclature, use Figures. A complete set of figures, preferably italics consistently for genotype symbols. Greater glossy photographs, should accompany each of the leniency can be allowed for phenotypic symbols. two copies of the manuscript. Graphs (submit as However, they should not be italicized. The pre- photographs) should be finished drawings not need- ferred convention is to use the same three-letter ing further artwork or type-setting. Absolutely no symbols in Roman type with the first letter capital- part of a graph should be typewritten (except the ized. legend, which should be typed on a separate page). Biochemical nomenclature, including abbrevia- Most graphs will be reduced to one-column width, tions and symbols, should follow the recommenda- and all elements in the drawing should be prepared tions of the IUPAC-IUB Commission on Biochemi- to withstand this reduction. The legend ofthe figure cal Nomenclature (CBN) and the Instructions to should provide enough information so that the Authors of J. Biol. Chem. and Arch. Biochem. figure is understandable without reference to the Biophys. (first issue of each year), which are based text. Experimental details from Materials and upon the CBN Recommendations and contain a list Methods should not be repeated in figure legends. thereof. Reprints of these Recommendations and Figure ordinate and abscissa scales, and table advice on biochemical and chemical nomenclature column headings, should avoid ambiguous use of are available from the NRC Office of Biochemical numbers with exponents (see p. 140, CBE Style Nomenclature (W. E. Cohn, Director), Biology Manual). Division, Oak Ridge Nat'l. Lab., Box Y, Oak Ridge, Nomenclature of microorganisms. In general, Tenn. 37830 (phone: 615-483-8611, Ext. 3-7514). the nomenclature presented in Bergey's Manual of Normally, abbreviations (except those of standard
Load more

Recommended publications
  • The Structure of Allophanate Hydrolase from Granulibacter Bethesdensis Provides Insights Into Substrate Specificity in the Amidase Signature Family
    Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications Biological Sciences, Department of 2013 The Structure of Allophanate Hydrolase from Granulibacter bethesdensis Provides Insights into Substrate Specificity in the Amidase Signature Family Yi Lin Marquette University, [email protected] Martin St. Maurice Marquette University, [email protected] Follow this and additional works at: https://epublications.marquette.edu/bio_fac Part of the Biochemistry, Biophysics, and Structural Biology Commons Recommended Citation Lin, Yi and St. Maurice, Martin, "The Structure of Allophanate Hydrolase from Granulibacter bethesdensis Provides Insights into Substrate Specificity in the Amidase Signature Family" (2013). Biological Sciences Faculty Research and Publications. 138. https://epublications.marquette.edu/bio_fac/138 Marquette University e-Publications@Marquette Biological Sciences Faculty Research and Publications/College of Arts and Sciences This paper is NOT THE PUBLISHED VERSION; but the author’s final, peer-reviewed manuscript. The published version may be accessed by following the link in the citation below. Biochemistry, Vol. 54, No. 4 (January 29, 2013): 690-700. DOI. This article is © American Chemical Society Publications and permission has been granted for this version to appear in e- Publications@Marquette. American Chemical Society Publications does not grant permission for this article to be further copied/distributed or hosted elsewhere without the express permission from American Chemical Society Publications. The Structure of Allophanate Hydrolase from Granulibacter bethesdensis Provides Insights into Substrate Specificity in the Amidase Signature Family Yi Lin Department of Biological Sciences, Marquette University, Milwaukee, WI Martin St. Maurice Department of Biological Sciences, Marquette University, Milwaukee, WI Abstract Allophanate hydrolase (AH) catalyzes the hydrolysis of allophanate, an intermediate in atrazine degradation and urea catabolism pathways, to NH3 and CO2.
    [Show full text]
  • Generated by SRI International Pathway Tools Version 25.0, Authors S
    Authors: Pallavi Subhraveti Ron Caspi Quang Ong Peter D Karp An online version of this diagram is available at BioCyc.org. Biosynthetic pathways are positioned in the left of the cytoplasm, degradative pathways on the right, and reactions not assigned to any pathway are in the far right of the cytoplasm. Transporters and membrane proteins are shown on the membrane. Ingrid Keseler Periplasmic (where appropriate) and extracellular reactions and proteins may also be shown. Pathways are colored according to their cellular function. Gcf_000725805Cyc: Streptomyces xanthophaeus Cellular Overview Connections between pathways are omitted for legibility.
    [Show full text]
  • Supplementary Information
    Supplementary information (a) (b) Figure S1. Resistant (a) and sensitive (b) gene scores plotted against subsystems involved in cell regulation. The small circles represent the individual hits and the large circles represent the mean of each subsystem. Each individual score signifies the mean of 12 trials – three biological and four technical. The p-value was calculated as a two-tailed t-test and significance was determined using the Benjamini-Hochberg procedure; false discovery rate was selected to be 0.1. Plots constructed using Pathway Tools, Omics Dashboard. Figure S2. Connectivity map displaying the predicted functional associations between the silver-resistant gene hits; disconnected gene hits not shown. The thicknesses of the lines indicate the degree of confidence prediction for the given interaction, based on fusion, co-occurrence, experimental and co-expression data. Figure produced using STRING (version 10.5) and a medium confidence score (approximate probability) of 0.4. Figure S3. Connectivity map displaying the predicted functional associations between the silver-sensitive gene hits; disconnected gene hits not shown. The thicknesses of the lines indicate the degree of confidence prediction for the given interaction, based on fusion, co-occurrence, experimental and co-expression data. Figure produced using STRING (version 10.5) and a medium confidence score (approximate probability) of 0.4. Figure S4. Metabolic overview of the pathways in Escherichia coli. The pathways involved in silver-resistance are coloured according to respective normalized score. Each individual score represents the mean of 12 trials – three biological and four technical. Amino acid – upward pointing triangle, carbohydrate – square, proteins – diamond, purines – vertical ellipse, cofactor – downward pointing triangle, tRNA – tee, and other – circle.
    [Show full text]
  • Supplementary Table S1. the Key Enzymes for Autotrophic Growth in C
    Electronic Supplementary Material (ESI) for Metallomics. This journal is © The Royal Society of Chemistry 2015 Supplementary Table S1. The key enzymes for autotrophic growth in C. metallidurans Name Rmet-number Spec. Predicted Mass, (kDa) Determined Mass, (kDa) Activity HOS Rmet_1522 to Rmet_1525 28.7 65.2, 25.4, 23.4, 52.8 = 166.8 62.4±1.8, 26.4±1.3, 24.0±0.6, 54.1±2.5, =235±20a HOP Rmet_1297, Rmet_1298, 67.0 69.0 + 38.6 = 108 148±24a CAX Rmet_1500, Rmet_1501 2.82 8 * (13.6 + 52.5) = 529 475±36a PRK Rmet_1512 0.994 8 * 32.4 = 259 256±11a aMean value of masses determined by S300 size exclusion chromatography and sucrose gradient centrifugation. HOS, NAD-reducing soluble hydrogenase; HOP, membrane-bound hydrogenase; CAX, ribulose-bis-phosphate carboxylase/oxygenase; PRK, phosphoribulokinase. Specific activity in U/mg protein. Supplementary Table S2. Genes expressed differently in AE104 compared to CH34 wild typea Operon Region Name Gene Q D Description UP Op1321r Rmet_4594 zntA 1.72 2.88 Q1LEH0 Heavy metal translocating P -type ATPase Op1322f Rmet_4595 czcI2 2.03 2.92 Q1LEG9 Putative uncharacterized protein Op1322f Rmet_4596 czcC2 23.34 5.36 Q1LEG8 Outer membrane efflux protein Op1322f Rmet_4597 czcB2' 15.36 9.68 Q1LEG7 Secretion protein HlyD Op0075f Rmet_0260 - 2.31 2.48 Q1LRT0 Putative transmembrane protein Op0075f Rmet_0261 coxB 2.08 2.49 Q1LRS9 Cytochrome c oxidase subunit 2 Adjacent to CMGI-7 Op0335f Rmet_1171 tnpA 7.03 21.74 Q9F8S6 Transposase (Transposase, IS4 family) CMGI-2 Op0362r Rmet_1251 tnp 4.08 0.61 Q1LNY9 Putative uncharacterized
    [Show full text]
  • 12) United States Patent (10
    US007635572B2 (12) UnitedO States Patent (10) Patent No.: US 7,635,572 B2 Zhou et al. (45) Date of Patent: Dec. 22, 2009 (54) METHODS FOR CONDUCTING ASSAYS FOR 5,506,121 A 4/1996 Skerra et al. ENZYME ACTIVITY ON PROTEIN 5,510,270 A 4/1996 Fodor et al. MICROARRAYS 5,512,492 A 4/1996 Herron et al. 5,516,635 A 5/1996 Ekins et al. (75) Inventors: Fang X. Zhou, New Haven, CT (US); 5,532,128 A 7/1996 Eggers Barry Schweitzer, Cheshire, CT (US) 5,538,897 A 7/1996 Yates, III et al. s s 5,541,070 A 7/1996 Kauvar (73) Assignee: Life Technologies Corporation, .. S.E. al Carlsbad, CA (US) 5,585,069 A 12/1996 Zanzucchi et al. 5,585,639 A 12/1996 Dorsel et al. (*) Notice: Subject to any disclaimer, the term of this 5,593,838 A 1/1997 Zanzucchi et al. patent is extended or adjusted under 35 5,605,662 A 2f1997 Heller et al. U.S.C. 154(b) by 0 days. 5,620,850 A 4/1997 Bamdad et al. 5,624,711 A 4/1997 Sundberg et al. (21) Appl. No.: 10/865,431 5,627,369 A 5/1997 Vestal et al. 5,629,213 A 5/1997 Kornguth et al. (22) Filed: Jun. 9, 2004 (Continued) (65) Prior Publication Data FOREIGN PATENT DOCUMENTS US 2005/O118665 A1 Jun. 2, 2005 EP 596421 10, 1993 EP 0619321 12/1994 (51) Int. Cl. EP O664452 7, 1995 CI2O 1/50 (2006.01) EP O818467 1, 1998 (52) U.S.
    [Show full text]
  • A Novel Decarboxylating Amidohydrolase Involved in Avoiding Metabolic Dead Ends During Cyanuric Acid Catabolism in Pseudomonas Sp
    RESEARCH ARTICLE A novel decarboxylating amidohydrolase involved in avoiding metabolic dead ends during cyanuric acid catabolism in Pseudomonas sp. strain ADP 1,2☯ 3☯ 2,3 1 Lygie Esquirol , Thomas S. PeatID , Matthew Wilding , Carol J. Hartley , 3 1,4 Janet Newman , Colin ScottID * a1111111111 1 Biocatalysis and Synthetic Biology Team, CSIRO Land & Water, Canberra, ACT, Australia, 2 Research School of Chemistry, Australian National University, Canberra, ACT, Australia, 3 CSIRO Biomedical a1111111111 Manufacturing, Parkville, Melbourne, VIC, Australia, 4 Synthetic Biology Future Science Platform, CSIRO a1111111111 Land & Water, Canberra, ACT, Australia a1111111111 a1111111111 ☯ These authors contributed equally to this work. * [email protected] Abstract OPEN ACCESS Citation: Esquirol L, Peat TS, Wilding M, Hartley Cyanuric acid is a common environmental contaminant and a metabolic intermediate in the CJ, Newman J, Scott C (2018) A novel catabolism of s-triazine compounds, including atrazine and other herbicides. Cyanuric acid decarboxylating amidohydrolase involved in is catabolized via a number of bacterial pathways, including one first identified in Pseudomo- avoiding metabolic dead ends during cyanuric acid nas sp. strain ADP, which is encoded by a single, five-gene operon (atzDGEHF) found on a catabolism in Pseudomonas sp. strain ADP. PLoS ONE 13(11): e0206949. https://doi.org/10.1371/ self-transmissible plasmid. The discovery of two of the five genes (atzG and atzH) was journal.pone.0206949 reported in 2018 and although the function of atzG was determined, the role of atzH was Editor: Monika Oberer, Karl-Franzens-Universitat unclear. Here, we present the first in vitro reconstruction of the complete, five-protein cyan- Graz, AUSTRIA uric acid catabolism pathway, which indicates that AtzH may be an amidase responsible for Received: August 29, 2018 converting 1,3-dicarboxyurea (the AtzE product) to allophanate (the AtzF substrate).
    [Show full text]
  • Supplementary Figure 1. Rpod Sequence Alignment. Protein Sequence Alignment Was Performed for Rpod from Three Species, Pseudoruegeria Sp
    J. Microbiol. Biotechnol. https://doi.org/10.4014/jmb.1911.11006 J. Microbiol. Biotechnol. https://doi.org/10.4014/jmb.2003.03025 Supplementary Figure 1. RpoD sequence alignment. Protein sequence alignment was performed for RpoD from three species, Pseudoruegeria sp. M32A2M (FPS10_24745, this study), Ruegeria pomeroyi (NCBI RefSeq: WP_011047484.1), and Escherichia coli (NCBI RefSeq: NP_417539.1). Multalin version 5.4.1 was used for the analysis. Subregion 2 and 4 are represented in a rectangle, and the helix-turn-helix motif in subregion 4 is highlighted in red. The amino acid degeneration from any of the three was highlighted in light gray and the sequence degeneration between Pseudoruegeria sp. M32A2M and R. pomeroyi is highlighted in dark gray. The substituted two amino acids into HTH motif (K578Q and D581S) against E. coli were marked as asterisk. Supplementary Table 1. Genome assembly statistics Categories Pseudoruegeria sp. M32A2M Number of scaffolds less than 1,000 bp 0 Number of scaffolds between 1,000 bp –10,000 bp 39 Number of scaffolds between 10,000 bp – 100,000 bp 38 Number of scaffolds larger than 100,000 bp 14 Number of scaffolds 91 Total assembled length (bp) 5,466,515 G+C contents (%) 62.4 N50 (bp) 249,384 Minimum length of scaffold (bp) 1,015 Maximum length of scaffold (bp) 733,566 Total Ns included in the draft genome 2,158 Supplementary Table 2. The list of gene annotation and its functional categorization in Pseudoruegeria sp.
    [Show full text]
  • Supplementary Information
    Supplementary Information Genomic analyses of Bifidobacterium moukalabense reveal adaptations to fruigivore/folivore feeding behavior Takahiro Segawa, Satoshi Fukuchi, Dylan Bodington, Sayaka Tsutida, Pierre Philippe Mbehang Nguema, Hishiro Mori, Kazunari Ushida This PDF file includes: Supplementary Figures 1-5 Supplementary Tables 1-10 GB03 GB04 95 GB01 Bifidobacterium moukalabense JCM 18751T (GG01T) 98 GB62 CD14 100 95 CD16 EB44 CD33 40 GB63 99 GB65 67 EB43 36 T Bifidobacterium catenulatum JCM 1194 99 T Bifidobacterium pseudocatenulatum JCM 1200 T Bifidobacterium merycicum JCM 8219 T Bifidobacterium dentium JCM 1195 T Bifidobacterium ruminantium JCM 8222 46 T Bifidobacterium faecale JCM 19861 100 T 37 Bifidobacterium adolescentis JCM 1275 56 41 T Bifidobacterium stercoris JCM 15918 T Bifidobacterium callitrichos JCM 17296 T Bifidobacterium kashiwanohense JCM 15439 T 45 Bifidobacterium biavatii JCM 17299 T Bifidobacterium bifidum JCM 1255 T 95 Bifidobacterium aesculapii JCM18761 T Bifidobacterium stellenboschense JCM 17298 T Bifidobacterium angulatum JCM 7096 72 T Bifidobacterium scardovii JCM 12489 T 100 Bifidobacterium gallinarum JCM 6291 100 T Bifidobacterium saeculare JCM 8223 T Bifidobacterium pullorum JCM 1214 T 60 Bifidobacterium animalis subsp. animalis JCM 1190 91 T Bifidobacterium choerinum JCM 1212 T 98 Bifidobacterium pseudolongum subsp. pseudolongum JCM 1205 T Bifidobacterium gallicum JCM 8224 T 63 Bifidobacterium cunniculi JCM 1213 77 T Bifidobacterium magnum JCM 1218 T 99 Bifidobacterium asteroids JCM 8230 69 T Bifidobacterium coryneforme JCM 5819 47 T Bifidobacterium actinocoloniiforme JCM 18048 T Bifidobacterium tsurumiense JCM 13495 T Bifidobacterium reuteri JCM 17295 T Bifidobacterium thermophilum JCM 1207 63 T 92 Bifidobacterium boum JCM 1211 96 T Bifidobacterium thermacidophilum subsp. thermacidophilum JCM 11165 T Bifidobacterium subtile DSM 20096 T Bifidobacterium lemurum JCM 30168 45 T Bifidobacterium breve JCM 1192 55 T Bifidobacterium saguini JCM 17297 68 Bifidobacterium indicum JCM 1302T 46 100 Bifidobacterium longum subsp.
    [Show full text]
  • Table S1. Fractional Pan-Genome of 10 CNS Genomes
    J. Microbiol. Biotechnol. https://doi.org/10.4014/jmb.1910.10049 jmb Table S1. Fractional pan-genome of 10 CNS genomes Product S. carnosus S. equorum S. succinus S. xylosus S. saprophyticus JCM 6069 TM300 KS1039 Mu2 14BME20 CSM 77 DSM 14617 C2a HKUOPL8 ATCC 15305 NAD(P)-dependent oxidoreductase BEK99_RS00020 SCA_RS11190 SE1039_RS10910 SEQMU2_RS02790 BK815_RS11650A6V26_RS07690AA913_RS01395 SXYL_RS02225BE24_RS09560 SSP_RS02040 FMN-binding glutamate synthase family protein BEK99_RS00025 SCA_RS11185 SE1039_RS10810 SEQMU2_RS02690 BK815_RS11780A6V26_RS07560AA913_RS01265 SXYL_RS02330BE24_RS09455 SSP_RS02140 drug:proton antiporter BEK99_RS00030 SCA_RS11180 SE1039_RS10625 SEQMU2_RS02505 BK815_RS11940A6V26_RS07400AA913_RS01105 SXYL_RS02520BE24_RS09255 SSP_RS02360 DUF1445 domain-containing protein BEK99_RS00060 SCA_RS11150 SE1039_RS11350 SEQMU2_RS03225 BK815_RS11200A6V26_RS08165AA913_RS03945 SXYL_RS01685BE24_RS10090 SSP_RS01500 TetR/AcrR family transcriptional regulator BEK99_RS00265 SCA_RS10980 SE1039_RS10455 SEQMU2_RS02315 BK815_RS12060A6V26_RS07280AA913_RS00980 SXYL_RS02715BE24_RS09060 SSP_RS02500 carbohydrate kinase BEK99_RS00270 SCA_RS10975 SE1039_RS08810 SEQMU2_RS00700 BK815_RS00585A6V26_RS12630AA913_RS13215 SXYL_RS04375BE24_RS07360 SSP_RS04170 MarR family transcriptional regulator BEK99_RS00315 SCA_RS10930 SE1039_RS12135 SEQMU2_RS03980 BK815_RS10515A6V26_RS08850AA913_RS09765 SXYL_RS00900BE24_RS10800 SSP_RS00840 pyruvate decarboxylase BEK99_RS00320 SCA_RS10925 SE1039_RS12125 SEQMU2_RS03970 BK815_RS10525A6V26_RS08840AA913_RS09775 SXYL_RS00905BE24_RS10795
    [Show full text]
  • Niche Strategy of Harmful Algae Revealed Through
    SUPPORTING I NFORMATION Niche of harmful alga Aureococcus anophagefferens revealed through ecogenomics; Gobler, C.J. et al MATERIALS AND METHODS 1. A. anophagefferens DNA isolation Eight 2-liter flasks with one liter of Aureococcus anophagefferens CCMP1984 culture each were grown axenically to mid-exponential growth phase (107 cells ml-1). The eight flasks were combined in a carboy and harvested with the Sharples continuous flow centrifuge. Cells were scraped from the mylar film, rinsed, and concentrated with a tabletop centrifuge to yield a wet weight of ~ 1 gram. The tube was temporarily stored in liquid N2 vapors. After temporary storage, the bottom half of the tube was placed in a 68º C water bath and heated enough to free the pellet from the tube at which point it was placed in a mortar filled with liquid nitrogen. The pellet was ground using a pestle, and placed into 5 different 50 mL plastic centrifuge tubes, to which Cetyltrimethyl Ammonium Bromide (CTAB) at 68º C was added. Beta-mercaptoethanol (1% final volume) was added to each tube. Tubes were periodically mixed by partial inversion and were incubated for three hours at 68ºC. An equal volume of phenol:chloroform:isoamyl alcohol (25:24:1 ratio) was then added to the cell suspension/CTAB. The tubes were mixed gently by partial inversion and centrifuged in a tabletop centrifuge. The aqueous fraction was removed and an equal volume of chloroform:isoamyl alcohol (24:1) was added and mixed by partial inversion, and then centrifuged. After the second chloroform extraction, the aqueous phase was transferred to a new tube and 0.6 volume of cold (-20º C) isopropanol was added.
    [Show full text]
  • 1471-2164-6-174-S4.PDF (299.1Kb)
    Sup_Table_2. Comparison of the whole genomes in Fig. 3A. Segment 1- Conserved in Bm, Bp, and Bt to Bp to Bt Gene Description % length % identity % length % identity BMA0001 chromosomal replication initiator protein DnaA 100 99 100 96 BMA0002 DNA polymerase III, beta subunit 100 100 100 99 BMA0003 DNA gyrase, B subunit 100 100 100 99 BMA0006 carboxymuconolactone decarboxylase family protein 100 98 100 99 BMA0010 hypothetical protein 100 99 100 92 BMA0011 hypothetical protein 100 100 100 91 BMA0014.1 hypothetical protein 100 99 96 94 BMA0018 hypothetical protein 100 99 100 95 BMA0019 FHA domain protein 100 100 100 94 BMA0020 protein kinase domain protein 100 99 100 90 BMA0023 conserved hypothetical protein 100 99 100 90 BMA0024 aldolase, class II 100 98 100 91 BMA0027 polysaccharide biosynthesis family protein 100 100 100 96 BMA0028 glycosyl transferase, group 1 family protein 100 99 100 94 BMA0029 mannose-1-phosphate guanylyltransferase/mannose-6-phosphate isomerase 100 99 100 92 BMA0030 ElaA family protein 100 99 100 90 BMA0032 glycosyl transferase, group 1 family protein 100 99 100 93 BMA0037 sigma-54 dependent transcriptional regulator 100 99 100 97 BMA0039 beta-mannosidase-related protein 100 99 100 91 BMA0040 conserved hypothetical protein 100 100 100 94 BMA0041 conserved hypothetical protein 100 99 100 95 BMA0042 acyl-CoA dehydrogenase domain protein 100 99 100 96 BMA0043 acyl carrier protein, putative 100 100 100 95 BMA0044 conserved hypothetical protein 100 99 100 96 BMA0045 conserved hypothetical protein 100 100 100 98 BMA0046
    [Show full text]
  • (12) Patent Application Publication (10) Pub. No.: US 2012/0266329 A1 Mathur Et Al
    US 2012026.6329A1 (19) United States (12) Patent Application Publication (10) Pub. No.: US 2012/0266329 A1 Mathur et al. (43) Pub. Date: Oct. 18, 2012 (54) NUCLEICACIDS AND PROTEINS AND CI2N 9/10 (2006.01) METHODS FOR MAKING AND USING THEMI CI2N 9/24 (2006.01) CI2N 9/02 (2006.01) (75) Inventors: Eric J. Mathur, Carlsbad, CA CI2N 9/06 (2006.01) (US); Cathy Chang, San Marcos, CI2P 2L/02 (2006.01) CA (US) CI2O I/04 (2006.01) CI2N 9/96 (2006.01) (73) Assignee: BP Corporation North America CI2N 5/82 (2006.01) Inc., Houston, TX (US) CI2N 15/53 (2006.01) CI2N IS/54 (2006.01) CI2N 15/57 2006.O1 (22) Filed: Feb. 20, 2012 CI2N IS/60 308: Related U.S. Application Data EN f :08: (62) Division of application No. 1 1/817,403, filed on May AOIH 5/00 (2006.01) 7, 2008, now Pat. No. 8,119,385, filed as application AOIH 5/10 (2006.01) No. PCT/US2006/007642 on Mar. 3, 2006. C07K I4/00 (2006.01) CI2N IS/II (2006.01) (60) Provisional application No. 60/658,984, filed on Mar. AOIH I/06 (2006.01) 4, 2005. CI2N 15/63 (2006.01) Publication Classification (52) U.S. Cl. ................... 800/293; 435/320.1; 435/252.3: 435/325; 435/254.11: 435/254.2:435/348; (51) Int. Cl. 435/419; 435/195; 435/196; 435/198: 435/233; CI2N 15/52 (2006.01) 435/201:435/232; 435/208; 435/227; 435/193; CI2N 15/85 (2006.01) 435/200; 435/189: 435/191: 435/69.1; 435/34; CI2N 5/86 (2006.01) 435/188:536/23.2; 435/468; 800/298; 800/320; CI2N 15/867 (2006.01) 800/317.2: 800/317.4: 800/320.3: 800/306; CI2N 5/864 (2006.01) 800/312 800/320.2: 800/317.3; 800/322; CI2N 5/8 (2006.01) 800/320.1; 530/350, 536/23.1: 800/278; 800/294 CI2N I/2 (2006.01) CI2N 5/10 (2006.01) (57) ABSTRACT CI2N L/15 (2006.01) CI2N I/19 (2006.01) The invention provides polypeptides, including enzymes, CI2N 9/14 (2006.01) structural proteins and binding proteins, polynucleotides CI2N 9/16 (2006.01) encoding these polypeptides, and methods of making and CI2N 9/20 (2006.01) using these polynucleotides and polypeptides.
    [Show full text]