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词条 Anabolism
释义

  1. Pathway

      Energy source    Cofactors    Substrates  

  2. Functions

      Anabolic hormones    Photosynthetic carbohydrate synthesis    Amino acid biosynthesis    Glycogen storage    Gluconeogenesis  

  3. Regulation

  4. Etymology

  5. References

Anabolism ({{IPAc-en|ə|ˈ|n|æ|b|ə|l|ɪ|s|m}}) is the set of metabolic pathways that construct molecules from smaller units.[1] These reactions require energy, known also as an endergonic process.[2] Anabolism is the building-up aspect of metabolism, whereas catabolism is the breaking-down aspect. Anabolism is usually synonymous with biosynthesis.

Pathway

Polymerization, an anabolic pathway used to build macromolecules such as nucleic acids, proteins, and polysaccharides, uses condensation reactions to join monomers.[3] Macromolecules are created from smaller molecules using enzymes and cofactors.

Energy source

Anabolism is powered by catabolism, where large molecules are broken down into smaller parts and then used up in cellular respiration. Many anabolic processes are powered by the cleavage of adenosine triphosphate (ATP).[4] Anabolism usually involves reduction and decreases entropy, making it unfavorable without energy input.[5] The starting materials, called the precursor molecules, are joined together using the chemical energy made available from hydrolyzing ATP, reducing the cofactors NAD+, NADP+, and FAD, or performing other favorable side reactions.[6] Occasionally it can also be driven by entropy without energy input, in cases like the formation of the phospholipid bilayer of a cell, where hydrophobic interactions aggregate the molecules.[7]

Cofactors

The reducing agents NADH, NADPH, and FADH2,[8] as well as metal ions,[3] act as cofactors at various steps in anabolic pathways. NADH, NADPH, and FADH2 act as electron carriers, while charged metal ions within enzymes stabilize charged functional groups on substrates.

Substrates

Substrates for anabolism are mostly intermediates taken from catabolic pathways during periods of high energy charge in the cell.[10]

Functions

Anabolic processes build organs and tissues. These processes produce growth and differentiation of cells and increase in body size, a process that involves synthesis of complex molecules. Examples of anabolic processes include the growth and mineralization of bone and increases in muscle mass.

Anabolic hormones

Endocrinologists have traditionally classified hormones as anabolic or catabolic, depending on which part of metabolism they stimulate. The classic anabolic hormones are the anabolic steroids, which stimulate protein synthesis and muscle growth, and insulin.

Photosynthetic carbohydrate synthesis

Photosynthetic carbohydrate synthesis in plants and certain bacteria is an anabolic process that produces glucose, cellulose, starch, lipids, and proteins from CO2.[5] It uses the energy produced from the light-driven reactions of photosynthesis, and creates the precursors to these large molecules via carbon assimilation in the photosynthetic carbon reduction cycle, a.k.a. the Calvin cycle.[10]

Amino acid biosynthesis

All amino acids are formed from intermediates in the catabolic processes of glycolysis, the citric acid cycle, or the pentose phosphate pathway. From glycolysis, glucose 6-phosphate is a precursor for histidine; 3-phosphoglycerate is a precursor for glycine and cysteine; phosphoenol pyruvate, combined with the 3-phosphoglycerate-derivative erythrose 4-phosphate, forms tryptophan, phenylalanine, and tyrosine; and pyruvate is a precursor for alanine, valine, leucine, and isoleucine. From the citric acid cycle, α-ketoglutarate is converted into glutamate and subsequently glutamine, proline, and arginine; and oxaloacetate is converted into aspartate and subsequently asparagine, methionine, threonine, and lysine.[10]

Glycogen storage

During periods of high blood sugar, glucose 6-phosphate from glycolysis is diverted to the glycogen-storing pathway. It is changed to glucose-1-phosphate by phosphoglucomutase and then to UDP-glucose by UTP--glucose-1-phosphate uridylyltransferase. Glycogen synthase adds this UDP-glucose to a glycogen chain.[10]

Gluconeogenesis

Glucagon is traditionally a catabolic hormone, but also stimulates the anabolic process of gluconeogenesis by the liver, and to a lesser extent the kidney cortex and intestines, during starvation to prevent low blood sugar.[8] It is the process of converting pyruvate into glucose. Pyruvate can come from the breakdown of glucose, lactate, amino acids, or glycerol.[9] The gluconeogenesis pathway has many reversible enzymatic processes in common with glycolysis, but it is not the process of glycolysis in reverse. It uses different irreversible enzymes to ensure the overall pathway runs in one direction only.[9]

Regulation

Anabolism operates with separate enzymes from catalysis, which undergo irreversible steps at some point in their pathways. This allows the cell to regulate the rate of production and prevent an infinite loop, also known as a futile cycle, from forming with catabolism.[10]

The balance between anabolism and catabolism is sensitive to ADP and ATP, otherwise known as the energy charge of the cell. High amounts of ATP cause cells to favor the anabolic pathway and slow catabolic activity, while excess ADP slows anabolism and favors catabolism.[10] These pathways are also regulated by circadian rhythms, with processes such as glycolysis fluctuating to match an animal's normal periods of activity throughout the day.[11]

Etymology

The word anabolism is from New Latin, which got the roots from {{lang-grc-gre|ἁνά}}, "upward" and {{lang|grc|βάλλειν}}, "to throw".

References

1. ^{{cite web|url=http://www.chem.qmul.ac.uk/iupac/bioinorg/AB.html#20|title=Glossary of Terms Used in Bioinorganic Chemistry: Anabolism | vauthors = de Bolster MW |year=1997 |publisher=International Union of Pure and Applied Chemistry |archive-url= https://web.archive.org/web/20071030105041/http://www.chem.qmul.ac.uk/iupac/bioinorg/AB.html |archive-date=30 October 2007 |deadurl=yes |access-date=2007-10-30}}
2. ^{{cite book | first1 = Connie | last1 = Rye | first2 = Robert | last2 = Wise | first3 = Vladimir | last3 = Jurukovski | first4 = Jung | last4 = Choi | first5 = Yael | last5 = Avissar | name-list-format = vanc |url= https://cnx.org/contents/GFy_h8cu@11.6:rZudN6XP@2/Introduction |title=Biology|last=|first= |year=2013 | publisher = OpenStax |location= Rice University, Houston Texas | isbn = 978-1-938168-09-3 }}
3. ^{{cite book |url= https://www.ncbi.nlm.nih.gov/books/NBK21054/ |title=Molecular Biology of the Cell |last=Alberts |first=Bruce |last2=Johnson |first2=Alexander |last3=Julian |first3=Lewis |last4=Raff |first4=Martin |last5=Roberts |first5=Keith |last6=Walter |first6=Peter | name-list-format = vanc |publisher=CRC Press |year=2002 |isbn=978-0-8153-3218-3|edition= 5th |location= |pages= |access-date=2018-11-01 |archive-url= https://archive.org/embed/MolecularBiologyOfTheCell5th |archive-date=6 June 2017}}
4. ^{{cite book | vauthors = Nicholls DG, Ferguson SJ |title=Bioenergetics | edition = 3rd |publisher=Academic Press | date = 2002 |isbn=978-0-12-518121-1}}
5. ^{{Cite book|url=https://biochem.science.oregonstate.edu/files/biochem/ahern/BiochemistryFreeandEasy3.pdf|title=Biochemistry Free and Easy|last=Ahern|first=Kevin|last2=Rajagopal|first2=Indira | name-list-format = vanc |publisher=Oregon State University|year=2013|isbn=|edition= 2nd|location=|pages=}}
6. ^{{Cite book | first1 = Donald | last1 = Voet | first2 = Judith G | last2 = Voet | first3 = Charlotte W | last3 = Pratt | name-list-format = vanc |url=https://www.worldcat.org/oclc/738349533|title=Fundamentals of biochemistry : life at the molecular level |date=2013|publisher=Wiley |isbn=978-0-470-54784-7|edition= Fourth |location=Hoboken, NJ |oclc=738349533}}
7. ^{{Cite book | first1 = Israel | last1 = Hanin | first2 = Giancarlo | last2 = Pepeu | name-list-format = vanc |url=https://www.worldcat.org/oclc/885405600 |title=Phospholipids: biochemical, pharmaceutical, and analytical considerations |isbn=978-1-4757-1364-0 |location=New York |oclc=885405600}}
8. ^{{cite book | chapter-url = https://bio.libretexts.org/TextMaps/Biochemistry/Book%3A_Biochemistry_Online_(Jakubowski)/10%3A_Metabolic_Pathways/B._MP2%3A_An_Overview_of_Metabolic_Pathways_-_Anabolism | chapter = An Overview of Metabolic Pathways - Anabolism |title=Biochemistry Online |last=Jakubowski |first=Henry | name-list-format = vanc |publisher=LibreTexts | location = College of St. Benedict, St. John's University|year=2002 }}
9. ^{{cite book | first1 = Jeremy M | last1 = Berg | first2 = John L | last2 = Tymoczko | first3 = Lubert | last3 = Stryer | name-list-format = vanc | url=https://www.worldcat.org/oclc/48055706 |title=Biochemistry|date=2002|publisher=W.H. Freeman |isbn=978-0-7167-3051-4 |edition=5th |location=New York|oclc=48055706}}
10. ^{{cite book | title=Principles of Biochemistry | first1 = David L | last1 = Nelson | first2 = Albert L | last2 = Lehninger | first3 = Michael M | last3 = Cox | name-list-format = vanc |year= 2013 |isbn=978-1-4292-3414-6|location= New York |publisher=W.H. Freeman |pages=}}
11. ^{{cite journal | vauthors = Ramsey KM, Marcheva B, Kohsaka A, Bass J | title = The clockwork of metabolism | journal = Annual Review of Nutrition | volume = 27 | issue = | pages = 219–40 | year = 2007 | pmid = 17430084 | doi = 10.1146/annurev.nutr.27.061406.093546 }}
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