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Biochemistry is a common university textbook used for teaching of biochemistry. It was initially written by Lubert Stryer and published by W. H. Freeman in 1975. [1] [2] [3] It has been published in regular editions since. [4] [5] [6] It is commonly used as an undergraduate teaching textbook or reference work. [7] [8]
Biochemistry is currently in its ninth edition and is widely used by many universities. He co-authored this book with John L. Tymoczko and Lubert Stryer, as well as Principles of Bioinorganic Chemistry with Stephen J. Lippard. He received the American Chemical Society ACS Award in Pure Chemistry in 1993.
Lubert Stryer (March 2, 1938 – April 8, 2024) was an American academic who was the Emeritus Mrs. George A. Winzer Professor of Cell Biology, at Stanford University School of Medicine. [ 1 ] [ 2 ] His research over more than four decades had been centered on the interplay of light and life.
Biochemistry – study of chemical processes in living organisms, ... and the Breast Cancer-2 gene ... 5th ed. Full text of Berg, Tymoczko, and Stryer, ...
Biochemistry, or biological chemistry, is the study of chemical processes within and relating to living organisms. [1] A sub-discipline of both chemistry and biology, biochemistry may be divided into three fields: structural biology, enzymology, and metabolism. Over the last decades of the 20th century, biochemistry has become successful at ...
Stryer5th is for referencing the 5th edition (2002) of Biohemistry by Lubert Stryer et al. It is based on the template {}. Parameters are: page (optional): to reference a single page; pages (optional): to reference multiple pages
Acetyl-CoA (acetyl coenzyme A) is a molecule that participates in many biochemical reactions in protein, carbohydrate and lipid metabolism. [2] Its main function is to deliver the acetyl group to the citric acid cycle (Krebs cycle) to be oxidized for energy production.
In animal tissue, BCKDC catalyzes an irreversible step [2] in the catabolism of the branched-chain amino acids L-isoleucine, L-valine, and L-leucine, acting on their deaminated derivatives (L-alpha-keto-beta-methylvalerate, alpha-ketoisovalerate, and alpha-ketoisocaproate, respectively) and converting them [3] to α-Methylbutyryl-CoA, Isobutyryl-CoA and Isovaleryl-CoA respectively.
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