Download Advanced Bacterial Genetics: Use of Transposons and Phage by Kelly Thomas Hughes, Sidney P. Colowick, Nathan Oram Kaplan, PDF

By Kelly Thomas Hughes, Sidney P. Colowick, Nathan Oram Kaplan, Stanley R. Maloy

The significantly acclaimed laboratory common for greater than fifty years, tools in Enzymology is among the such a lot hugely revered guides within the box of biochemistry. considering 1955, each one quantity has been eagerly awaited, often consulted, and praised through researchers and reviewers alike. Now with over four hundred volumes (all of them nonetheless in print), the sequence comprises a lot fabric nonetheless appropriate today-truly a necessary booklet for researchers in all fields of existence sciences. This new quantity offers equipment with regards to using bacterial genetics for genomic engineering. The publication comprises sections on pressure collections and genetic nomenclature; transposons; and phage.

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Extra info for Advanced Bacterial Genetics: Use of Transposons and Phage for Genomic Engineering

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Striped box represents the transposon. Leftward and rightward arrows represent primers for sequencing transposon‐chromosome junctions. [4] identification of essential genes in bacteria 21 References Goryshin, I. , and Reznikoff, W. S. (1998). Tn5 in vitro transposition. J. Biol. Chem. 273, 7367–7374. Goryshin, I. , Hoffman, L. , and Reznikoff, W. S. (2000). Insertional transposon mutagenesis by electroporation of released Tn5 transposition complexes. Nature Biotech. 18, 97–100. [4] Identification of Essential Genes in Bacteria By DAVID R.

A proposal for a uniform nomenclature in bacterial genetics. Genetics 54, 61–76. , and Hartman, P. (1968). A proposal for a uniform nomenclature in bacterial genetics. J. Gen. Microbiol. 50, 1–14. , and Friefelder, D. (1994). ‘‘Microbial Genetics,’’ 2nd ed. Jones and Bartlett Publishers, Boston. , and Taylor, R. (1996). ’’ Cold Spring Harbor Laboratory Press, NY. Schmid, M. , and Roth, J. R. (1983). Genetic methods for analysis and manipulation of inversion mutations in bacteria. Genetics 105, 517–537.

1996). 6. Prepare P22‐transducing lysates on each insertion mutant.

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