chembox new
ImageFile= Tyrocidine.pngImageSize= 300px
IUPACName= 3-((3S,6R,9S,12S,15S,18S,21S,24S,27R,32aS)-9-(2-amino-2-oxoethyl)-21-(3-aminopropyl)-3,6,27-tribenzyl-15-(4-hydroxybenzyl)-24-isobutyl-18-isopropyl-1,4,7,10,13,16,19,22,25,28-decaoxodotriacontahydropyrrolo [1,2-a] [1,4,7,10,13,16,19,22,25,28] decaazacyclotriacontin-12-yl)propanamide.
Section1=Chembox Identifiers
CASNo= 8011-61-8
PubChem= 16129635

Section2=Chembox Properties

Tyrocidine is a mixture of cyclic decapeptides produced by the bacteria "Bacillus brevis" found in soil. It can be composed of 4 different amino acid sequences, giving tyrocidine A-D. (See figure 1). Tyrocidine is the major constituent of tyrothricin, which also contains gramicidinPubchem: Tyrocidine and Tyrothricin. cite web |url=http://www.ncbi.nlm.nih.gov/sites/entrez?term=16129635%5Buid%5D&cmd=search&db=pccompound |title=PubChem Compound Result |format= |work= |accessdate=] . Tyrocidine was the first commercially available antibiotic, but has been found to be toxic toward human blood and reproductive cells. The function of tyrocidine within its host ‘’B. brevis’’ is thought to be regulation of sporulation cite journal |author=Mootz HD, Marahiel MA |title=The tyrocidine biosynthesis operon of Bacillus brevis: complete nucleotide sequence and biochemical characterization of functional internal adenylation domains |journal=J. Bacteriol. |volume=179 |issue=21 |pages=6843–50 |year=1997 |month=November |pmid=9352938 |doi= |url=http://jb.asm.org/cgi/pmidlookup?view=long&pmid=9352938] .

Tyrocidines A, B, and C are cyclic decapeptides. The biosynthesis of tyrocidine involves three enzymes. Parts of its sequence are identical to gramicidin S.


In 1939 the American microbiologist René Dubos discovered the soil microbe "Bacillus brevis". He observed the ability of the microbe to decompose the capsule of pneumococcus bacterium, rendering it harmless. From the soil microbe "B. brevis" he isolated tyrothricin which had a high toxicity to a large range of bacteria. Tyrothricin was later found to be a mixture of the peptides gramicidin and tyrocidine. These were observed to have toxic effects in red blood cells and reproductive cells in humans, however if applied externally as an ointment tyrocidine could be used as a potent antimicrobial agent [cite encyclopedia
title =Antibiotics
encyclopedia = The Columbia Electronic Encyclopedia
volume = 6th ed.
pages = online
publisher = Columbia University Press
date = 2007
id =
accessdate = May 2008
] Dubos's discovery helped revive interest in research on penicillin.

Mechanism of Action

Tyrocidine has a unique mode of action in which it disrupts the cell membrane function, making it a favorable target for engineering derivatives cite journal |author=Qin C, Bu X, Wu X, Guo Z |title=A chemical approach to generate molecular diversity based on the scaffold of cyclic decapeptide antibiotic tyrocidine A |journal=J Comb Chem |volume=5 |issue=4 |pages=353–5 |year=2003 |pmid=12857101 |doi=10.1021/cc0300255 |url=] . Tyrocidine appears to perturb the lipid bilayer of a microbe’s inner membrane through permeating the lipid phase of the membrane. Further studies need to be performed in order to determine the affinity and location of tyrocidine within the phospholipid bilayer [cite journal |author=Prenner EJ, Lewis RN, McElhaney RN |title=The interaction of the antimicrobial peptide gramicidin S with lipid bilayer model and biological membranes |journal=Biochim. Biophys. Acta |volume=1462 |issue=1-2 |pages=201–21 |year=1999 |month=December |pmid=10590309 |doi= |url=http://linkinghub.elsevier.com/retrieve/pii/S0005-2736(99)00207-2] .


The biosynthesis of Tyrocidine is similar to Gramicidin S, and is achieved through the use of nonribosomal protein synthetases (NRPSs) cite journal |author=Kopp F, Marahiel MA |title=Macrocyclization strategies in polyketide and nonribosomal peptide biosynthesis |journal=Nat Prod Rep |volume=24 |issue=4 |pages=735–49 |year=2007 |month=August |pmid=17653357 |doi=10.1039/b613652b |url=] . Its biosynthesis is accomplished through enzymatic assembly consisting of 3 peptide synthetase proteins, TycA, TycB, and TycC, which contain 10 modules. It is important to note that the tyrocidine analogues (A-D) are not produced by different enzymes, but rather by an enzyme system which is capable of incorporating different amino acids of structural similarity at specified sites. The amino acid sequence is determined by the organization of the enzyme and not by any RNA template [cite journal |author=Roskoski R, Gevers W, Kleinkauf H, Lipmann F |title=Tyrocidine biosynthesis by three complementary fractions from Bacillus brevis (ATCC 8185) |journal=Biochemistry |volume=9 |issue=25 |pages=4839–45 |year=1970 |month=December |pmid=4320358 |doi= |url=] . The tyrocine synthetases TycA, TycB, and TycC are encoded on the tyrocine operon. This consists of the three genes encoding for the three synthetases as well as three additional open reading frames (ORFs). These ORFs, labeled as TycD, TycE, and TycF are downstream of the three synthetase genes (see figure 2). TycD &TycE have the highest similarity to members of the ATP-binding cassette (ABC) transporter family which aid in the transport of substrates across a membrane. It has been suggested that the tandem transporters play a role in conferring resistance in the producer cell through tyrocidine secretion. TycF has been identified as a thioesterase (TE) and is similar to other TEs in bacterial operons used for encoding peptide synthetases. However, the precise function of these TEs remains unknown . The size of the peptide synthetases corresponds to the amount of activation they carry out. TycA is the smallest and activates a single amino acid from one module, TycB is intermediate in size and activates 3 amino acids with 3 modules, and TycC is the largest and activates 6 amino acids with 6 modules (See figure 3) .Each module performs all the catalytic reactions necessary to incorporate a single amino acid onto the peptide chain. This is accomplished through the subdomains for adenylation (A), peptityl carrier protein (PCP), condensation (C), and depending on the amino acid position, an epimerization (E). The adenylation subdomain is used in activating the specific amino acid. Each module uses one molecule of the selected substrate amino acid with one molecule of ATP to give an aminoacyl adenylate enzyme complex and pyrophosphate. The activated amino acid can then be transferred to the enzyme bound 4'-phosphopantetheine of the carrier protein with the expulsion of AMP from the system. The carrier protein uses the 4’-phosphopantetheine prosthetic group for loading of the growing peptide and their monomer precursors cite journal |author=Kohli RM, Walsh CT, Burkart MD |title=Biomimetic synthesis and optimization of cyclic peptide antibiotics |journal=Nature |volume=418 |issue=6898 |pages=658–61 |year=2002 |month=August |pmid=12167866 |doi=10.1038/nature00907 |url=] . Elongation of the peptide chain is achieved through condensation of the upstream PCP onto an adjacent downstream PCP-bound monomer. In certain domains you will find modification subdomains, such as the E subdomain seen in domains 1 and 4 in tyrocidine, which will generate the D-configured amino acid. On the final module is the TE domain used as a catalyst for cyclization or product release. The release of the product from the carrier protein is achieved through acylation of the active site serine of TE in which the decapeptide is transferred from the thiol ether to the serine residue. Deacylation can then occur through intramolecular cyclization or through hydrolysis to give the cyclic or linear product respectively (See figure 4). In the case of tyrocidine, ring closure has been shown to be highly favorable due to 4 H-bonds helping the decapeptide backbone to adopt a stable conformation (See figure 5) . This intramolecular cyclization occurs in a head-to-tail fashion involving the N-terminus of the D-Phe1 and the C-terminus of the L-Leu10 (See figure 4) [cite journal |author=Trauger JW, Kohli RM, Mootz HD, Marahiel MA, Walsh CT |title=Peptide cyclization catalysed by the thioesterase domain of tyrocidine synthetase |journal=Nature |volume=407 |issue=6801 |pages=215–8 |year=2000 |month=September |pmid=11001063 |doi=10.1038/35025116 |url=] .

Chemoenzymatic Strategies

There is no chemical solution for macrocyclization of a peptide chain. Isolated tyrocidine (Tyc) TE domains can be used to cyclize chemically derived peptidyl-thioester substrates, providing a powerful route to new cyclic compounds. In order for this macrocyclization to occur the peptides must be C-terminally activated with an N-acethylcysteamine (SNAC) leaving group . An “alanine-scan” through the 10 positions of tyrocidine shows that only the D-Phe and L-Orn are required for sufficient cyclization. Tyc TE can also be used biomimetically in which it mimics the environment created by the TE domain with the substrate’s PCP through use of a synthetic tether linked to a polyethylene glycol (PEG) amide resin . Use of this resin bound to a desired substrate with isolated TE can allow for catalytic release of the resin as well as macrocyclization of the substrate (See figure 6 ). Use of solid phase peptide synthesis (SPPS) can be utilized in the incorporation of a diverse array of monomers into the peptide chain. Later studies used the high tolerance of Tyc TE in order to modify the peptide backbone post-synthetically. This also allowed for glycosylation of the tyrosine or serine residues to be incorporated . Use of these methods has led to many promising new therapeutic agents.


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  • tyrocidine — [tī΄rō sīd′ n, tī΄rəsī′dēn΄] n. [ TYRO(SINE) + CID(E) + INE3] an antibacterial substance obtained from a soil bacillus (Bacillus brevis) …   English World dictionary

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  • tyrocidine — also tyrocidin noun Etymology: tyrothricin + gramicidin Date: 1940 a basic polypeptide antibiotic produced by a soil bacillus (Bacillus brevis) …   New Collegiate Dictionary

  • tyrocidine — noun a polypeptide antibiotic produced by bacteria in the soil …   Wiktionary

  • tyrocidine — ty·ro·ci·dine also ty·ro·ci·din .tī rə sīd ən n a basic polypeptide antibiotic produced by a soil bacterium of the genus Bacillus (B. brevis) and constituting the major component of tyrothricin * * * ty·ro·ci·dine (ti″ro siґdin) a… …   Medical dictionary

  • tyrocidine — n. antibiotic medication extracted from tyrothricin (Pharmacology) …   English contemporary dictionary

  • tyrocidine — ty·ro·ci·dine …   English syllables

  • tyrocidine — noun a basic polypeptide antibiotic derived from a soil bacterium; a major component of tyrothricin • Syn: ↑tyrocidin • Hypernyms: ↑antibiotic, ↑antibiotic drug • Substance Holonyms: ↑tyrothricin …   Useful english dictionary

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