Cyanophycin, also known as CGP (cyanophycin granule polypeptide) or multi-L-arginyl-poly (L-aspartic acid), is a non-protein, non-ribosomally produced amino acid polymer composed of an aspartic acid backbone and arginine side groups.
Cyanophycin was first detected in 1887 by the Italian botanist Antonino Borzì and can be found in most cyanobacteria and a few heterotrophic bacteria such as Acinetobacter sp.[1] Cyanophycin is largely insoluble under physiological conditions and is accumulated in the form of granules in the cytoplasm during phosphate or sulfur starvation, generally in the early and mid-stationary phase. It is used as a nitrogen- and possibly carbon-storage compound and also serves as a dynamic buffer for fixed nitrogen in cyanobacterial heterocysts. Nitrogen and carbon are mobilized from cyanophycin by intracellular cyanophycinase in the form of aspartate-arginine dipeptides.
Cyanophycin is synthesized from arginine and aspartate in an ATP-dependent reaction catalyzed by a single enzyme, cyanophycin synthetase.[2] Cyanophycin is of potential interest to biotechnology as a source of polyaspartic acid. Due to its unusual polyamphoteric character, cyanophycin is soluble in water under acidic (0.1 M HCl) and alkaline conditions. Heterologous expression of cyanophycin synthetase allows production of cyanophycin in a number of biotechnologically relevant bacteria such as Escherichia coli and Corynebacterium glutamicum.[3]
Since insoluble forms of CGP are easily purified, most studies have overlooked the synthesis of CGP that is soluble at a neutral pH. To compare the two, insoluble CGP can be solubilized by only weak acids while soluble CGP can be separated with the process of precipitation by using acetone or ethanol.[4] In 2014, an experiment by Steinbüchel and Wiefel determined that the amount of lysine residue can regulate the solubility of cyanophycin, with higher levels of lysine negatively correlating to the temperature needed to make the polymer soluble with aqueous solvents.[4] It was concluded that insoluble and soluble CGP are not distinct polymers, since they originate from the same polymer mixture, but are instead classified as mixes of cyanophycin mixtures with varying concentrations of lysine residues.
The ability of lysine to partially replace the arginine side chain encouraged research of CGP variants with amino acids such as ornithine and citrulline. Lysine, ornithine and citrulline all have an affinity for cyanophycin synthase (L-aspartate-adding) enzyme CphA.[4] Wiefel, Bröker and Steinbüchel conducted an experiment demonstrating that citrulline-rich cyanophycin can be produced through the introduction of a citrulline-producing strain.[5] It was also determined that insoluble CGP only exhibited minuscule concentrations of citrulline while soluble CGP was able to produce a high concentration of citrulline. This trend is also similar for ornithine.
YouTube Encyclopedic
-
1/3Views:5 3393391 417
-
Cyanobacteria
-
In search of the perfect grain: sensory evaluation of rice by consumers
-
Rice Quality Evaluation: Khao Dawk Mali 105 vs. Apo & a Dilemma for Breeders
Transcription
References
- ^ Krehenbrink M, Oppermann-Sanio FB, Steinbüchel A (May 2002). "Evaluation of non-cyanobacterial genome sequences for occurrence of genes encoding proteins homologous to cyanophycin synthetase and cloning of an active cyanophycin synthetase from Acinetobacter sp. strain DSM 587". Archives of Microbiology. 177 (5): 371–80. doi:10.1007/s00203-001-0396-9. PMID 11976746. S2CID 2072408.
- ^ Ziegler K, Diener A, Herpin C, Richter R, Deutzmann R, Lockau W (May 1998). "Molecular characterization of cyanophycin synthetase, the enzyme catalyzing the biosynthesis of the cyanobacterial reserve material multi-L-arginyl-poly-L-aspartate (cyanophycin)". European Journal of Biochemistry. 254 (1): 154–9. doi:10.1046/j.1432-1327.1998.2540154.x. PMID 9652408.
- ^ Oppermann-Sanio FB, Steinbüchel A (January 2002). "Occurrence, functions and biosynthesis of polyamides in microorganisms and biotechnological production". Die Naturwissenschaften. 89 (1): 11–22. Bibcode:2002NW.....89...11O. doi:10.1007/s00114-001-0280-0. PMID 12008968. S2CID 21405793.
- ^ a b c Wiefel L, Steinbüchel A (February 2014). "Solubility behavior of cyanophycin depending on lysine content". Applied and Environmental Microbiology. 80 (3): 1091–6. doi:10.1128/AEM.03159-13. PMC 3911199. PMID 24271185.
- ^ Wiefel L, Bröker A, Steinbüchel A (June 2011). "Synthesis of a citrulline-rich cyanophycin by use of Pseudomonas putida ATCC 4359". Applied Microbiology and Biotechnology. 90 (5): 1755–62. doi:10.1007/s00253-011-3224-4. PMID 21455592. S2CID 21008673.
This page was last edited on 20 February 2024, at 14:32