Tina M. Henkin - Snyder and Champness Molecular Genetics of Bacteria

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The single most comprehensive and authoritative textbook on bacterial molecular genetics Snyder & Champness Molecular Genetics of Bacteria In an era experiencing an avalanche of new genetic sequence information, this updated edition presents important experiments and advanced material relevant to current applications of molecular genetics, including conclusions from and applications of genomics; the relationships among recombination, replication, and repair and the importance of organizing sequences in DNA; the mechanisms of regulation of gene expression; the newest advances in bacterial cell biology; and the coordination of cellular processes during the bacterial cell cycle. The topics are integrated throughout with biochemical, genomic, and structural information, allowing readers to gain a deeper understanding of modern bacterial molecular genetics and its relationship to other fields of modern biology.
Although the text is centered on the most-studied bacteria,
and
, many examples are drawn from other bacteria of experimental, medical, ecological, and biotechnological importance. The book's many useful features include
Text boxes to help students make connections to relevant topics related to other organisms, including humans A summary of main points at the end of each chapter Questions for discussion and independent thought A list of suggested readings for background and further investigation in each chapter Fully illustrated with detailed diagrams and photos in full color A glossary of terms highlighted in the text While intended as an undergraduate or beginning graduate textbook, Molecular Genetics of Bacteria is an invaluable reference for anyone working in the fields of microbiology, genetics, biochemistry, bioengineering, medicine, molecular biology, and biotechnology.
"This is a marvelous textbook that is completely up-to-date and comprehensive, but not overwhelming. The clear prose and excellent figures make it ideal for use in teaching bacterial molecular genetics."—
, University of Washington

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QUESTIONS FOR THOUGHT

1 1. Some viruses, such as adenovirus, avoid the problem of lagging-strand synthesis by replicating the individual strands of the DNA in the leading-strand direction simultaneously from both ends so that eventually the entire molecule is replicated. Why do bacterial chromosomes not replicate in this way?

2 2. Why are DNA molecules so long? Would it not be easier to have many shorter pieces of DNA? What are the advantages and disadvantages of a single long DNA molecule?

3 3. Why do cells have DNA as their hereditary material instead of RNA, like some viruses?

4 4. What effect would shifting a temperature-sensitive mutant with a mutation in the dnaA gene for initiator protein DnaA have on the rate of DNA synthesis? Would the rate drop linearly or exponentially? Would the slope of the curve be affected by the growth rate of the cells at the time of the shift? Explain.

5 5. The gyrase inhibitor novobiocin inhibits the growth of almost all types of bacteria. What would you predict about the gyrase of the bacterium Streptomyces sphaeroides, which makes this antibiotic? How would you test your hypothesis?

6 6. How do you think chromosome replication and cell division are coordinated in bacteria like E. coli? How would you go about testing your hypothesis?

7 7. Why is termination of chromosome replication so sloppy that the ter region is nonessential for growth and there has to be more than one ter site in each direction to completely stop the replication fork? What are the advantages of not having a definite site on the chromosome at which replication always terminates?

SUGGESTED READING

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8 Cortez D, Quevillon-Cheruel S, Gribaldo S, Desnoues N, Sezonov G, Forterre P, Serre M-CM. 2010. Evidence for a Xer/dif system for chromosome resolution in archaea. PLoS Genet 6:e1001166.

9 Dervyn E, Suski C, Daniel R, Bruand C, Chapuis J, Errington J, Jannière L, Ehrlich SD. 2001. Two essential DNA polymerases at the bacterial replication fork. Science 294:1716–1719.

10 Dohrmann PR, Correa R, Frisch RL, Rosenberg SM, McHenry CS. 2016. The DNA polymerase III holoenzyme contains γ and is not a trimeric polymerase. Nucleic Acids Res 44:1285–1297.

11 Fournes F, Val M-E, Skovgaard O, Mazel D. 2018. Replicate once per cell cycle: replication control of secondary chromosomes. Front Microbiol 9:1833.

12 Fricker AD, Peters JE. 2014. Vulnerabilities on the lagging-strand template: opportunities for mobile elements. Annu Rev Genet 48:167–186.

13 Fujimitsu K, Senriuchi T, Katayama T. 2009. Specific genomic sequences of E. coli promote replicational initiation by directly reactivating ADP-DnaA. Genes Dev 23:1221–1233.

14 Gabbai CB, Yeeles JTP, Marians KJ. 2014. Replisome-mediated translesion synthesis and leading strand template lesion skipping are competing bypass mechanisms. J Biol Chem 289:32811–32823.

15 Galli E, Ferat J-L, Desfontaines J-M, Val M-E, Skovgaard O, Barre FX, Possoz C. 2019. Replication termination without a replication fork trap. Sci Rep 9:8315. http://doi.org/10.1038/s41598-019-43795-2

16 Guy CP, Atkinson J, Gupta MK, Mahdi AA, Gwynn EJ, Rudolph CJ, Moon PB, van Knippenberg IC, Cadman CJ, Dillingham MS, Lloyd RG, McGlynn P. 2009. Rep provides a second motor at the replisome to promote duplication of protein-bound DNA. Mol Cell 36:654–666.

17 Hayama R, Marians KJ. 2010. Physical and functional interaction between the condensin MukB and the decatenase topoisomerase IV in Escherichia coli. Proc Natl Acad Sci USA 107:18826–18831.

18 Heller RC, Marians KJ. 2006. Replication fork reactivation downstream of a blocked nascent leading strand. Nature 439:557–562.

19 Helmstetter CE, Cooper S. 1968. DNA synthesis during the division cycle of rapidly growing Escherichia coli B/r. J Mol Biol 31:507–518.

20 Jean NK, Rutherford TJ, Löwe J. 2019. FtsK in motion reveals its mechanism for doublestranded DNA translocation. bioRxiv 1–24.

21 Joshi MC, Magnan D, Montminy TP, Lies M, Stepankiw N, Bates D. 2013. Regulation of sister chromosome cohesion by the replication fork tracking protein SeqA. PLoS Genet 9:e1003673.

22 Kasho K, Katayama T. 2013. DnaA binding locus datA promotes DnaA-ATP hydrolysis to enable cell cycle-coordinated replication initiation. Proc Natl Acad Sci USA 110:936–941.

23 Kohanski MA, Dwyer DJ, Hayete B, Lawrence CA, Collins JJ. 2007. A common mechanism of cellular death induced by bactericidal antibiotics. Cell 130:797–810.

24 Kysela DT, Randich AM, Caccamo PD, Brun YV. 2016. Diversity takes shape: understanding the mechanistic and adaptive basis of bacterial morphology. PLoS Biol 14:e1002565.

25 Le Bourgeois P, Bugarel M, Campo N, Daveran-Mingot M-L, Labonté J, Lanfranchi D, Lautier T, Pagès C, Ritzenthaler P. 2007. The unconventional Xer recombination machinery of streptococci/lactococci. PLoS Genet 3:e117.

26 Liu N-J, Dutton RJ, Pogliano K. 2006. Evidence that the SpoIIIE DNA translocase participates in membrane fusion during cytokinesis and engulfment. Mol Microbiol 59:1097–1113.

27 Mercier R, Petit MA, Schbath S, Robin S, El Karoui M, Boccard F, Espéli O. 2008. The MatP/matS site-specific system organizes the terminus region of the E. coli chromosome into a macrodomain. Cell 135:475–485.

28 Moolman MC, Krishnan ST, Kerssemakers JWJ, van den Berg A, Tulinski P, Depken M, Reyes-Lamothe R, Sherratt DJ, Dekker NH. 2014. Slow unloading leads to DNA-bound β2-sliding clamp accumulation in live Escherichia coli cells. Nat Commun 5:5820.

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30 Olby R. 1974. The Path to the Double Helix. Macmillan Press, London, United Kingdom.

31 Pomerantz RT, O'Donnell M. 2008. The replisome uses mRNA as a primer after colliding with RNA polymerase. Nature 456:762–766.

32 Postow L, Hardy CD, Arsuaga J, Cozzarelli NR. 2004. Topological domain structure of the Escherichia coli chromosome. Genes Dev 18: 1766–1779.

33 Reddy CA, Beveridge TJ, Breznak JA, Marzluf G, Schmidt TM, Snyder LR (ed). 2007. Methods for General and Molecular Microbiology, 3rd ed. ASM Press, Washington, DC.

34 Reyes-Lamothe R, Sherratt DJ, Leake MC. 2010. Stoichiometry and architecture of active DNA replication machinery in Escherichia coli. Science 328:498–501.

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