|
|
|
|
LEADER |
05304nam a2200613 4500 |
001 |
ocn815495803 |
003 |
OCoLC |
005 |
20180501122004.0 |
006 |
m o d |
007 |
cr cnu---unuuu |
008 |
121010s2012 cauaf ob 001 0 eng d |
040 |
|
|
|a E7B
|b eng
|e pn
|c E7B
|d OCLCO
|d N$T
|d COF
|d BUF
|d CUS
|d OPELS
|d YDXCP
|d OPELS
|d OCLCF
|d VVL
|d KUK
|d EBLCP
|d MHW
|d UKDOC
|d DEBSZ
|d VVL
|d OCLCQ
|d D6H
|d OCLCQ
|d MERER
|d OCLCQ
|d TFH
|d OCLCO
|d OCLCA
|d NJR
|d OCLCO
|d OCLCQ
|d GrThAP
|
019 |
|
|
|a 815653073
|a 818817000
|
020 |
|
|
|a 9780123946287
|q (electronic bk.)
|
020 |
|
|
|a 012394628X
|q (electronic bk.)
|
020 |
|
|
|a 9780123942913
|
035 |
|
|
|a (OCoLC)815495803
|z (OCoLC)815653073
|z (OCoLC)818817000
|
050 |
|
4 |
|a QR88.3
|b .N38 2012eb
|
072 |
|
7 |
|a SCI
|x 007000
|2 bisacsh
|
082 |
0 |
4 |
|a 572.45
|2 23
|
049 |
|
|
|a TEFA
|
245 |
0 |
0 |
|a Natural product biosynthesis by microorganisms and plants.
|n Part B /
|c edited by David A. Hopwood.
|
260 |
|
|
|a San Diego, Calif. :
|b Elsevier,
|c 2012.
|
300 |
|
|
|a 1 online resource (lvi, 393 pages, [12] pages of color plates :) :
|b illustrations (some color).
|
336 |
|
|
|a text
|b txt
|2 rdacontent
|
337 |
|
|
|a computer
|b c
|2 rdamedia
|
338 |
|
|
|a online resource
|b cr
|2 rdacarrier
|
490 |
1 |
|
|a Methods in enzymology,
|x 0076-6879 ;
|v v. 516
|
504 |
|
|
|a Includes bibliographical references and index.
|
505 |
0 |
|
|a In vivo production of thiopeptide variants / Feifei Zhang and Wendy L. Kelly -- Microviridin biosynthesis / Thomas K. Hemscheidt -- Cyclotide isolation and characterization / David J. Craik, Sonia Troeira Henriques, Joshua S. Mylne, and Conan K. Wang -- Ribosomally encoded cyclic peptide toxins from mushrooms / Jonathan D. Walton, Hong Luo, and Heather Hallen-Adams -- The Pictet-Spengler mechanism involved in the biosynthesis of tetrahydroisoquinoline antitumor antibiotics: a novel function for a nonribosomal peptide synthetase / Kento Koketsu [and others] -- Discovery and biosynthesis of phosphonate and phosphinate natural products / Spencer C. Peck, Jiangtao Gao, and Wilfred A van der Donk -- RlmN and AtsB as models for the overproduction and characterization of radical SAM proteins / Nicholas D. Lanz [and others] -- Fe(II)-dependent, uridine-5'-monophosphate [alpha]-ketoglutarate dioxygenases in the synthesis of 5'-modified nucleosides / Zhaoyong Yang, Jason Unrine, Koichi Nonaka, and Steven G. Van Lanen.
|
505 |
0 |
|
|a Tailoring reactions catalyzed by heme-dependent enzymes: spectroscopic characterization of the L-tryptophan-nitrating cytochrome P450 TxtE / Sarah M. Barry and Gregory L. Challis -- Oxidative tailoring reactions: catalyzed by nonheme iron-dependent enzymes: streptorubin B biosynthesis as an example / Paulina K. Sydor and Gregory L. Challis -- The rare fluorinated natural products and biotechnological prospects for fluorine enzymology / K.K. Jason Chan and David O'Hagan -- Enzymatic chlorination and bromination / Karl-Heinz van Pée -- Prenyltransferases of the dimethylallyltryptophan synthase superfamily / Xia Yu and Shu-Ming Li -- Serine carboxypeptidase-like acyltransferases from plants / Sam T. Mugford and Carsten Milkowski -- 4-methylideneimidazole-5-one-containing aminomutases in enediyne biosynthesis / Jeremy R. Lohman and Ben Shen -- Tailoring enzymes acting on carrier protein-tethered substrates in natural product biosynthesis / Shuangjun Lin, Tingting Huang, and Ben Shen -- High-throughput colorimetric assays for nucleotide sugar formation and glycosyl transfer / Richard W. Gantt and Jon S. Thorson.
|
588 |
0 |
|
|a Print version record.
|
520 |
|
|
|a This new volume of Methods in Enzymology continues the legacy of this premier serial by containing quality chapters authored by leaders in the field. The second of 3 volumes covering Natural product biosynthesis by microorganisms and plants. This new volume continues the legacy of this premier serialContains quality chapters authored by leaders in the field The second of 3 volumes it has chapters on such topics as biological chlorination, bromination and iodination, and phylogenetic approaches to natural product structure prediction.
|
650 |
|
0 |
|a Microbiological synthesis.
|
650 |
|
0 |
|a Plant products
|x Synthesis.
|
650 |
|
0 |
|a Biosynthesis.
|
650 |
|
0 |
|a Enzymes.
|
650 |
|
7 |
|a SCIENCE
|x Life Sciences
|x Biochemistry.
|2 bisacsh
|
650 |
|
7 |
|a Biosynthesis.
|2 fast
|0 (OCoLC)fst00832721
|
650 |
|
7 |
|a Enzymes.
|2 fast
|0 (OCoLC)fst00913605
|
650 |
|
7 |
|a Microbiological synthesis.
|2 fast
|0 (OCoLC)fst01019572
|
650 |
|
7 |
|a Plant products
|x Synthesis.
|2 fast
|0 (OCoLC)fst01065651
|
650 |
|
2 |
|a Chemistry Techniques, Synthetic
|x methods.
|
650 |
|
2 |
|a Peptide Biosynthesis, Nucleic Acid-Independent.
|
650 |
1 |
2 |
|a Biosynthetic Pathways
|v Laboratory Manuals.
|
650 |
2 |
2 |
|a Plants
|x enzymology
|v Laboratory Manuals.
|
650 |
2 |
2 |
|a Bacteria
|x enzymology
|v Laboratory Manuals.
|
650 |
2 |
2 |
|a Fungi
|x enzymology
|v Laboratory Manuals.
|
655 |
|
4 |
|a Electronic books.
|
655 |
|
7 |
|a Electronic books.
|2 lcgft
|
700 |
1 |
|
|a Hopwood, D. A.
|
776 |
0 |
8 |
|i Print version:
|a Hopwood, David A.
|t Natural Product Biosynthesis by Microorganisms and Plants Part B.
|d Burlington : Elsevier Science, ©2012
|z 9780123942913
|
830 |
|
0 |
|a Methods in enzymology ;
|v volume 516.
|
856 |
4 |
0 |
|u https://www.sciencedirect.com/science/bookseries/00766879/516
|z Full Text via HEAL-Link
|