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Glyoxylate cycle

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Overview of the Glyoxylate Cycle

The glyoxylate cycle, a variation of the tricarboxylic acid cycle, is an anabolic pathway occurring in plants, bacteria, protists, and fungi. The glyoxylate cycle centers on the conversion of acetyl-CoA to succinate for the synthesis of carbohydrates.[1] In microorganisms, the glyoxylate cycle allows cells to utilize simple carbon compounds as a carbon source when complex sources such as glucose are not available.[2] The cycle is generally assumed to be absent in animals, with the exception of nematodes at the early stages of embryogenesis. In recent years, however, the detection of malate synthase (MS) and isocitrate lyase (ICL), key enzymes involved in the glyoxylate cycle, in some animal tissue has raised questions regarding the evolutionary relationship of enzymes in bacteria and animals and suggests that animals encode alternative enzymes of the cycle that differ in function from known MS and ICL in non-metazoan species.[1][3]

Similarities with TCA cycle

The glyoxylate cycle utilizes five of the eight enzymes associated with the tricarboxylic acid cycle: citrate synthase, aconitase, succinate dehydrogenase, fumarase, and malate dehydrogenase. The two cycles differ in that in the glyoxylate cycle, isocitrate is converted into glyoxylate and succinate by ICL instead of into α-ketoglutarate.[1] This bypasses the decarboxylation steps that take place in the TCA cycle, allowing simple carbon compounds to be used in the later synthesis of macromolecules, including glucose.[2] Glyoxylate is subsequently combined with acetyl-CoA to produce malate, catalyzed by MS.[1] Malate is also formed in parallel from succinate by the action of succinate dehydrogenase and fumarase.

Structure of intermediates in Fischer projections and polygonal model

The intermediates of glyoxylate cycle depicted in Fischer projections show the chemical changing step by step. Such image can be compared to polygonal model representation.[4]

Structure of intermediates of glyoxylate cycle showed using Fischer projections, left, and polygonal model, right. Two-carbon molecule acetyl in the activated form acetyl-CoA (AcoA), on the top, condensate with four carbon molecule oxaloacetate (OxA) to form citrate (Cit). The next intermediates are, respectively, cis-aconitate (CisA) and isocitrate (IsoC), which produces succinate (Suc) and glyoxylate (Glx). The last condensate with two-carbon molecule from another acetyl-CoA, producing malate (Mal), with regeneration of the oxaloacetate. The enzymes involved in this pathway correspond to citrate synthase (1), aconitase (2), isocitrate lyase (3), malate synthase (4) and malate dehydrogenase (5). Notably two molecules de acetyl-CoA produce one molecule of succinate, which can be used to carbohydrate synthesis. Succinate can produce oxaloacetate by reactions of citric acid cycle (succinate – fumarate – malate – oxaloacetate), not represented here. Coenzymes (CoA-SH, NAD+, NADH + H+) were omitted in these representations. The productions of NADH from the oxidized forms of coenzymes is represented as the release of "2H".

Role in gluconeogenesis

Fatty acids from lipids are commonly used as an energy source by vertebrates as fatty acids are degraded through beta oxidation into acetate molecules. This acetate, bound to the active thiol group of coenzyme A, enters the citric acid cycle (TCA cycle) where it is fully oxidized to carbon dioxide. This pathway thus allows cells to obtain energy from fat. To utilize acetate from fat for biosynthesis of carbohydrates, the glyoxylate cycle, whose initial reactions are identical to the TCA cycle, is used.

Cell-wall containing organisms, such as plants, fungi, and bacteria, require very large amounts of carbohydrates during growth for the biosynthesis of complex structural polysaccharides, such as cellulose, glucans, and chitin. In these organisms, in the absence of available carbohydrates (for example, in certain microbial environments or during seed germination in plants), the glyoxylate cycle permits the synthesis of glucose from lipids via acetate generated in fatty acid β-oxidation.

The glyoxylate cycle bypasses the steps in the citric acid cycle where carbon is lost in the form of CO2. The two initial steps of the glyoxylate cycle are identical to those in the citric acid cycle: acetate → citrate → isocitrate. In the next step, catalyzed by the first glyoxylate cycle enzyme, isocitrate lyase, isocitrate undergoes cleavage into succinate and glyoxylate (the latter gives the cycle its name). Glyoxylate condenses with acetyl-CoA (a step catalyzed by malate synthase), yielding malate. Both malate and oxaloacetate can be converted into phosphoenolpyruvate, which is the product of phosphoenolpyruvate carboxykinase, the first enzyme in gluconeogenesis. The net result of the glyoxylate cycle is therefore the production of glucose from fatty acids. Succinate generated in the first step can enter into the citric acid cycle to eventually form oxaloacetate.[2]

Function in organisms

Plants

In plants the glyoxylate cycle occurs in special peroxisomes which are called glyoxysomes. This cycle allows seeds to use lipids as a source of energy to form the shoot during germination. The seed cannot produce biomass using photosynthesis because of lack of an organ to perform this function. The lipid stores of germinating seeds are used for the formation of the carbohydrates that fuel the growth and development of the organism.

The glyoxylate cycle can also provide plants with another aspect of metabolic diversity. This cycle allows plants to take in acetate both as a carbon source and as a source of energy. Acetate is converted to Acetyl CoA (similar to the TCA cycle). This Acetyl CoA can proceed through the glyoxylate cycle, and some succinate is released during the cycle. The four carbon succinate molecule can be transformed into a variety of carbohydrates through combinations of other metabolic processes; the plant can synthesize molecules using acetate as a source for carbon. The Acetyl CoA can also react with glyoxylate to produce some NADPH from NADP+, which is used to drive energy synthesis in the form of ATP later in the Electron Transport Chain. [5]

Pathogenic fungi

The glyoxylate cycle may serve an entirely different purpose in some species of pathogenic fungi. The levels of the main enzymes of the glyoxylate cycle, ICL and MS, are greatly increased upon contact with a human host. Mutants of a particular species of fungi that lacked ICL were also significantly less virulent in studies with mice compared to the wild type. The exact link between these two observations is still being explored, but it can be concluded that the glyoxylate cycle is a significant factor in the pathogenesis of these microbes.[6][7]

Vertebrates

Vertebrates were once thought to be unable to perform this cycle because there was no evidence of its two key enzymes, isocitrate lyase and malate synthase. However, some research suggests that this pathway may exist in some, if not all, vertebrates. [8] [9] Specifically, some studies show evidence of components of the glyoxylate cycle existing in significant amounts in the liver tissue of chickens. Data such as these support the idea that the cycle could theoretically occur in even the most complex vertebrates.[10] Other experiments have also provided evidence that the cycle is present among certain insect and marine invertebrate species, as well as strong evidence of the cycle's presence in nematode species. However, other experiments refute this claim.[11] Some publications conflict on the presence of the cycle in mammals: for example, one paper has stated that the glyoxalate cycle is active in hibernating bears,[12] but this report was disputed in a later paper.[13] Evidence exists for malate synthase activity in humans due to a dual functional malate/B-methylmalate synthase of mitochondrial origin called CLYBL expressed in brown fat and kidney.[14] Vitamin D may regulate this pathway in vertebrates.[10][15]

Inhibition of the glyoxylate cycle

Due to the central role of the glyoxylate cycle in the metabolism of pathogenic species including fungi and bacteria, enzymes of the glyoxylate cycle are current inhibition targets for the treatment of diseases. Most reported inhibitors of the glyoxylate cycle target the first enzyme of the cycle (ICL). Inhibitors were reported for Candida albicans for potential use as antifungal agents.[16] The mycobacterial glyoxylate cycle is also being targeted for potential treatments of tuberculosis.[17][18]

Engineering concepts

The prospect of engineering various metabolic pathways into mammals which do not possess them is a topic of great interest for bio-engineers today. The glyoxylate cycle is one of the pathways which engineers have attempted to manipulate into mammalian cells. This is primarily of interest for engineers in order to increase the production of wool in sheep, which is limited by the access to stores of glucose. By introducing the pathway into sheep, the large stores of acetate in cells could be used in order to synthesize glucose through the cycle, allowing for increased production of wool.[19] Mammals are incapable of executing the pathway due to the lack of two enzymes, isocitrate lyase and malate synthase, which are needed in order for the cycle to take place. It is believed by some that the genes to produce these enzymes, however, are pseudogenic in mammals, meaning that the gene is not necessarily absent, rather, it is merely "turned off".[1]

In order to engineer the pathway into cells, the genes responsible for coding for the enzymes had to be isolated and sequenced, which was done using the bacteria E.coli, from which the AceA gene, responsible for encoding for isocitrate lyase, and the AceB gene, responsible for encoding for malate synthase were sequenced.[19] Engineers have been able to successfully incorporate the AceA and AceB genes into mammalian cells in culture, and the cells were successful in translating and transcribing the genes into the appropriate enzymes, proving that the genes could successfully be incorporated into the cell’s DNA without damaging the functionality or health of the cell. However, being able to engineer the pathway into transgenic mice has proven to be difficult for engineers. While the DNA has been expressed in some tissues, including the liver and small intestine in test animals, the level of expression is not high, and not found to be statistically significant. In order to successfully engineer the pathway, engineers would have to fuse the gene with promoters which could be regulated in order to increase the level of expression, and have the expression in the right cells, such as epithelial cells.[20]

Efforts to engineer the pathway into more complex animals, such as sheep, have not been effective. This illustrates that much more research needs to be done on the topic, and suggests it is possible that a high expression of the cycle in animals would not be tolerated by the chemistry of the cell. Incorporating the cycle into mammals will benefit from advances in nuclear transfer technology, which will enable engineers to examine and access the pathway for functional integration within the genome before its transfer to animals.[19]

There are possible benefits, however, to the cycle's absence in mammalian cells. The cycle is present in microorganisms that cause disease but is absent in mammals, for example humans. There is a strong plausibility of the development of antibiotics that would attack the glyoxylate cycle, which would kill the disease-causing microorganisms that depend on the cycle for their survival, yet would not harm humans where the cycle, and thus the enzymes that the antibiotic would target, are absent.[2]

References

  1. ^ a b c d e Kondrashov, Fyodor A; Koonin, Eugene V; Morgunov, Igor G; Finogenova, Tatiana V; Kondrashova, Marie N; Morgunov, I. G.; Finogenova, T. V.; Kondrashova, M. N. (23 October 2006). "Evolution of glyoxylate cycle enzymes in Metazoa: evidence of multiple horizontal transfer events and pseudogene formation". Biology Direct. 1: 31. doi:10.1186/1745-6150-1-31. PMC 1630690. PMID 17059607.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: unflagged free DOI (link)
  2. ^ a b c d Lorenz, Michael; Fink, Gerald; (October 2002). "Life and Death in a Macrophage: Role of the Glyoxylate Cycle in Virulence". Eukaryotic Cell. 1 (5): 657–662. doi:10.1128/EC.1.5.657-662.2002. PMC 126751. PMID 12455685.{{cite journal}}: CS1 maint: extra punctuation (link) CS1 maint: multiple names: authors list (link)
  3. ^ Popov, EA; Moskalev, EA; Shevchenko, MU; Eprintsev, AT (November 2005). "Comparative analysis of glyoxylate cycle key enzyme isocitrate lyase from organisms of different systematic groups". Journal of Evolutionary Biochemistry and Physiology. 41 (6): 631–639. doi:10.1007/s10893-006-0004-3.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  4. ^ Bonafe, CFS; de Jesus MB; Bispo JAC (January–February 2018), "The Polygonal Model: A Simple Representation of Biomolecules as a Tool for Teaching Metabolism", Biochemistry and Molecular Biology Education, 46 (1): 66–75, doi:10.1002/bmb.21093{{citation}}: CS1 maint: date format (link)
  5. ^ Berg JM, Tymoczko JL, Stryer L (2002). Biochemistry. New York: W. H. Freeman.
  6. ^ Lorenz, Michael; Fink, Gerald (July 2001). "The Glyoxylate Cycle is Required for Fungal Virulence". Nature. 412 (6842): 83–86. doi:10.1038/35083594. PMID 11452311.
  7. ^ Dunn, M. F.; Ramírez-Trujillo, J. A.; Hernández-Lucas, I. (October 2009). "Major roles of isocitrate lyase and malate synthase in bacterial and fungal pathogenesis". Microbiology. 155: 3166–3175. doi:10.1099/mic.0.030858-0. PMID 19684068.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  8. ^ V. N. Popov; E. A. Moskalev; M. U. Shevchenko; A. T. Eprintsev (December 2005). "Comparative Analysis of Glyoxylate Cycle Key Enzyme Isocitrate Lyase from Organisms of Different Systematic Groups". Journal of Evolutionary Biochemistry and Physiology. 41 (6).
  9. ^ Davis WL, Goodman DB; Goodman (December 1992). "Evidence for the glyoxylate cycle in human". The Anatomical Record. 234 (4): 461–8. doi:10.1002/ar.1092340402. PMID 1456449.
  10. ^ a b David, WL; Jones RG; Farmer GR; Dickerson T; Cortinas E; Cooper OJ; Crawford L; Goodman DB (1990). "Identification of Glyoxylate Cycle Enzmes in Chick Liver". Anat. Rec. 227 (3): 271–284. doi:10.1002/ar.1092270302. PMID 2164796.
  11. ^ Storrey, Kenneth, ed. (2004). Functional Metabolism: Regulation and Adaption. Hobocken, New Jersey: John Wiley and Sons, Inc. pp. 221–223. ISBN 0-471-41090-X.
  12. ^ Davis WL, Goodman DB, Crawford LA, Cooper OJ, Matthews JL; Goodman; Crawford; Cooper; Matthews (March 1990). "Hibernation activates glyoxylate cycle and gluconeogenesis in black bear brown adipose tissue". Biochim. Biophys. Acta. 1051 (3): 276–8. doi:10.1016/0167-4889(90)90133-X. PMID 2310778.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  13. ^ Jones JD, Burnett P, Zollman P; Burnett; Zollman (October 1999). "The glyoxylate cycle: does it function in the dormant or active bear?". Comp. Biochem. Physiol. B, Biochem. Mol. Biol. 124 (2): 177–9. doi:10.1016/S0305-0491(99)00109-1. PMID 10584301.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  14. ^ Strittmatter L1, Li Y, Nakatsuka NJ, Calvo SE, Grabarek Z, Mootha VK (2014). "CLYBL is a polymorphic human enzyme with malate synthase and β-methylmalate synthase activity". Human Molecular Genetics. 23: 2313–23. doi:10.1093/hmg/ddt624. PMC 3976331. PMID 24334609.{{cite journal}}: CS1 maint: multiple names: authors list (link) CS1 maint: numeric names: authors list (link)
  15. ^ Davis WL, Jones RG, Farmer GR, Cortinas E, Matthews JL, Goodman DB; Jones; Farmer; Cortinas; Matthews; Goodman (1989). "The glyoxylate cycle in rat epiphyseal cartilage: the effect of vitamin-D3 on the activity of the enzymes isocitrate lyase and malate synthase". Bone. 10 (3): 201–6. doi:10.1016/8756-3282(89)90054-9. PMID 2553083.{{cite journal}}: CS1 maint: multiple names: authors list (link)
  16. ^ Cheah, HL; Lim, V; Sandai D (Apr 2014). "Inhibitors of the glyoxylate cycle enzyme ICL1 in Candida albicans for potential use as antifungal agents". PLOS ONE. 9 (4): :e95951. doi:10.1371/journal.pone.0095951. PMC 4004578. PMID 24781056.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  17. ^ Bhusal, RP; Bashiri, G; Kwai, BXC; Sperry, J; Leung, IKH (Jul 2017). "Targeting isocitrate lyase for the treatment of latent tuberculosis". Drug Discov. Today. 22 (7): 1008–1016. doi:10.1016/j.drudis.2017.04.012. PMID 28458043.
  18. ^ Lee, Y-V; Wahab, HA; Choong, YS (2015). "Potential Inhibitors for Isocitrate Lyase of Mycobacterium tuberculosis and Non-M. tuberculosis: A Summary". BioMed. Res. Int. 2015: 895453. doi:10.1155/2015/895453.{{cite journal}}: CS1 maint: unflagged free DOI (link)
  19. ^ a b c Ward, Kevin (2000). "Transgene-mediated modifications to animal biochemistry". Trends in Biotechnology. 18 (3): 99–102. doi:10.1016/S0167-7799(99)01417-1. PMID 10675896. Retrieved 2011-03-31.
  20. ^ Ward, Kevin; C. D. Nancarrow (1 Sep 1991). "The genetic engineering of production traits in domestic animals". Cellular and Molecular Life Sciences. 47 (9): 913–922. doi:10.1007/BF01929882.
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