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Bacterial and Bacteriophage Genetics: An Introduction PDF

431 Pages·1988·11.592 MB·English
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A* (rfe) b1oP* 56 ""• 66 nUpG 76 86 (rffl ufebxiBe,•O ,E* 96 sfrB* -~~~~~:~! rl"'Gl rrnG rriG -fcsA* iteT core• p~h~e~A~ l qrrlstWG notbtB P*I, P7 ------prorntA A t rrrrfiAA opryo Ir --l~f ,rp.,iS. ceo l --o-t-t-P~2fU~ ~~1 svabioSA * 57 QrpE 67 rdpnsaUG 77 87 97 leu X rpoO (monC) ottP4* ottl86 (nmD) oobCPor-• * ----i nosahiBA * --rho --UUIKIUU -A-f ----l~t hyd* 58 envQ* 68 78 88 98 --p•IA,B,C alaS t -~if~~~ sriR 0 mt• --hsd--i~l ...... . .rp, sOt dodO* infB dnaT 59 69 aroG 79 89 99 -~dnoC iop• docB ftsH* cys~~ rptu• -tsr ;---n rkpbmaA' * -r~mi etrrpreenyni1tAoAGx•- •* gpaglo lztnBogF •e* • 'lttJ"yhiyr'r"UTT j pcsdtfireeehrpotro A,BR Md yt e, fe11A~.~, msp, 60 70 rnpB 80 90 tufB ~~rsrrA·I~! 100 Springer Series in Microbiology Edward A. Birge Bacterial and Bacteriophage Genetics An Introduction Second Edition With 150 Figures • Springer Science+Business Media, LLC Edward A. Birge Department of Microbiology Arizona State University Tempe. Arizona 85287 LIBRARY OF CONGRESS Library of Congress Cataloging-in-Publication Data Birge. Edward A. (Edward Asahel) . Bacterial and bacteriophage genetics : an introduction I Edward A. Birge.-2nd ed. p. cm.-(Springer series in microbiology) Inc1udes bibliographies and index. ISBN 978-1-4757-1997-0 ISBN 978-1-4757-1995-6 (eBook) DOI 10.1007/978-1-4757-1995-6 1. Bacterial genetics. 2. Bacteriophage-Genetics. 1. Title. Il. Series. [DNLM: 1. Bacteria-genetics. 2. Bacteriophages-genetics. QW 51 B617b] QH434.B57 1988 589.9'OI5-dcI9 DNLMlDLC for Library of Congress 88-12241 CIP © 1981, 1988 by Springer Science+Business Media New York Originally published by Springer-Verlag New York, Inc. in 1988 Softcover reprint of the hardcover 2nd edition 1988 AII rights reserved. This work may not be translated or copied in whole or in part without the written permis sion of the publisher Springer Science+Business Media, LLC. except for brief excerpts in connection with reviews or scholarly analysis. Use in connection with any form ofinformation storage and retrieval. electronic adaptation, computer software. or by similar or dis similar methodology now known or hereafter developed is forbidden. The use of general descriptive names, trade names, trademarks. etc. in this publication, even ifthe former are not especially identified, is not to be taken as a sign that such names. as understood by the Trade Marks and Merchandise Marks Act, may accordingly be used freely by anyone. Typeset by David E. Seham Associates/Metuchen, New Jersey. 9 8 7 6 5 4 3 2 1 ISBN 978-1-4757-1997-0 For Lori, Anna, and Colin Preface to the Second Edition It is with real pleasure that I offer some introductory remarks to this second edition of Bacterial and Bacteriophage Genetics. The reception of the first edition was very good, and most of the criticisms offered have only served to strengthen this new edition. The majority of the suggestions for revision of material included requests for more molecular detail. I have tried to provide this throughout the text but especially in the heavily revised Chapter I and completely rewritten Chapters 2 and 10. The former Chapter 2 has been repositioned as an appendix so as to offer an uninterrupted flow of material in the main body of the text. The tremendous increase in our knowledge of the genetics of eukaryotic microorganisms has permitted another sort of change in coverage. Instead of general discussions about eukaryotic organisms, wherever possible I have tried to offer specific details about Saccharomyces cerevisiae, whose wealth of genetic detail will soon rival that of Escherichia coli. Although this material is not intended as a substitute for a course in yeast genetics, it is my hope that it will enable the beginning student to comprehend some of the similarities and differences between these two popular micro organisms. As before this book is intended for the student who is taking a first course in bacterial and bacteriophage genetics and who brings to it some background in genetics. The best background would be an introductory course in general genetics, but extensive coverage of genetics in an in troductory biology course might well prove sufficient. As an example, it is assumed that the student is familiar with the standard Watson and Crick model for DNA structure. A broad knowledge of microorganisms is helpful but not required to understand the material presented. In general the ma terial from a good introductory biology course should be adequate. viii Preface to the Second Edition Several books can be noted as being particularly useful sources of de tailed supplementary information. David Freifelder's Physical Biochem istry, Second Edition, is particularly valuable as a resource for methods used in analyzing macromolecules. Additional information about Saccha romyces can be found in Yeast Genetics: Fundamental and Applied As pects edited by J.F.T. Spencer, D.M. Spencer, and A.R.W. Smith. Cold Spring Harbor Laboratory constantly publishes many monographs dealing with various aspects of bacterial and viral genetics. Their current book list should be consulted for details. Probably the most important one for this book is Genetic Maps, Volume 4, edited by S.J. O'Brien. The Amer ican Society for Microbiology also is a good source for monographic lit erature. Their recent publications include Escherichia coli and Salmonella typhimurium: Cell and Molecular Biology, edited by F.W. Neidhardt. Most references to classic papers have been omitted, and the reader is referred to collections of papers that have been reprinted such as the volume edited by Abou-Sabe. Acknowledgments I am indebted to many people for helpful suggestions and comments about the first edition. I would particularly like to acknowledge the following individuals who assisted in correcting errors in the first edition: Dr. Paul A. Lemke, Auburn University; Dr. Margarita Salas, Universidad Auton oma de Madrid; and Dr. T.A. Trautner, Max Planck lnstitut, Berlin. Dr. W. Scott Champney's suggestions on reorganizing the material were most helpful. Dr. Martha Howe graciously volunteered some assistance with the material on phage Mu. However, any errors that remain must be at tributed to me. It has once again been a pleasure to work with the people at Springer Verlag who have been very helpful during all phases of this revision. Linkage Maps Inside the front cover The illustrations on the front inside cover are linear scale drawings representing the circular linkage map of E. coli K-12. The time scale of 100 minutes, beginning arbitrarily with zero at the thr locus, is based on the results of interrupted-conjugation experi ments. Major genetic symbols used in this figure are defined in Table 2- 2. Parentheses around a gene symbol indicate that the position of that marker is not well known and may have been determined only within 5 to 10 minutes. An asterisk indicates that a marker has been mapped more precisely but that its position with respect to nearby markers is not known. The small vertical arrows indicate the directions of transcription of certain well-studied loci. Parentheses around an operon indicate that, although the direction of transcription of the genes in the operon is known, the orientation of the operon on the chromosome is not known. A similar map for Salmonella typhimurium may be found inside the back cover. From Bachmann, B.J. (1983) Linkage map of E. coli K-12, edition VII. Micro biological Reviews 47:180-230. Inside the back cover The illustrations on the back inside cover are linear scale drawings representing the circular linkage map of Salmonella ty phimurium. The scale of 100 units has been chosen to emphasize the sim ilarities to the E. coli map (inside the front cover). A length of one unit represents the amount of DNA carried by P22, KBl, or ES18 transducing phage particles, while a length of two units represents the amount of DNA carried by a PI transducing phage particle (see Chapter 7). The segmented lines to the right of the gene symbols indicate genes that are jointly trans duced and the linear distances determined from these data. Major genetic

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