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Tunicamycin

Tunicamycin is a mixture of homologous nucleoside antibiotics produced by several species of ''Streptomyces'' bacteria, including ''Streptomyces clavuligerus'' and ''Streptomyces lysosuperificus''.^[1] It functions as a potent inhibitor of the enzyme UDP-N-acetylglucosamine:dolichyl-phosphate N-acetylglucosamine-1-phosphate transferase (DPAGT1) in eukaryotes, thereby blocking the first step in N-linked protein glycosylation and inducing endoplasmic reticulum stress.^[1] In bacteria, it targets polyprenylphosphate-N-acetyl-hexosamine-1-phosphotransferases (PNPTs), disrupting cell wall biosynthesis and exhibiting activity against Gram-positive bacteria and mycobacteria.^[2] Due to its high toxicity to eukaryotic cells, tunicamycin is primarily employed as an experimental tool in research to study the unfolded protein response (UPR), cell cycle arrest in the G1 phase, and glycosylation-related pathways, rather than as a therapeutic agent.^[1] As of 2024, research has focused on tunicamycin derivatives to mitigate its eukaryotic toxicity while preserving antibacterial efficacy, such as TunR2, which features reduced double bonds and a dihydrouracil substitution, showing promise in models of Mycobacterium infections with minimal host cell impact.^[2] More recent studies as of 2025 have explored nanoencapsulation to reduce toxicity for potential oncology applications.^[3] Despite these advances and ongoing challenges with toxicity, specificity, and delivery, tunicamycin remains mainly a biochemical probe for investigating glycoprotein folding and ER homeostasis.^[4]

Discovery and Production

Discovery

Tunicamycin was first discovered in 1971 by Japanese researchers Akira Takatsuki, Kei Arima, and Gakuzo Tamura at the University of Tokyo, who isolated it from the culture filtrates of a newly identified strain, Streptomyces lysosuperificus nov. sp.^[5] The compound emerged during routine screening of microbial metabolites for novel antimicrobial agents, where it demonstrated potent inhibitory activity against animal and plant viruses, as well as antifungal effects on yeast and Gram-positive bacteria.^[5] The isolation process involved extracting the active substance from the fermentation broth using solvent partitioning, followed by purification through silicic acid column chromatography, yielding a white powder with an approximate molecular weight of 870.^[5] Early characterization revealed it as a mixture of closely related nucleoside antibiotics, distinguished by its ultraviolet absorption spectrum indicative of a uracil moiety and its solubility properties.^[5] The researchers named it "tunicamycin," derived from tunica (Latin for coat), reflecting its inhibitory action on the formation of viral envelopes and bacterial cell walls.^[5] A key milestone in the 1970s was the structural elucidation of tunicamycin, achieved in 1977 by Takatsuki and colleagues through acid hydrolysis, chromatographic separation, and spectroscopic analysis, which confirmed its unique core consisting of a uracil-linked aminodeoxypentitol sugar attached to an N-acetylglucosamine and a fatty acid chain.^[6] This work highlighted the compound's heterogeneity as a mixture of homologues differing in fatty acid length, solidifying its classification as a nucleoside antibiotic with unprecedented structural features.^[6]

Producing Organisms

Tunicamycin is primarily produced by the actinomycete bacterium Streptomyces lysosuperificus ATCC 31396, from which the antibiotic was originally isolated as a mixture of homologs.^[7] Another key primary producer is Streptomyces clavuligerus NRRL 3585, which synthesizes tunicamycin alongside other secondary metabolites like clavulanic acid.^[8] Secondary production occurs in Streptomyces chartreusis strains NRRL 3882 and NRRL 12338, which accumulate tunicamycin at higher concentrations than the primary producers under optimized conditions.^[8] Additional Streptomyces species, such as S. griseus ATCC 31591 and certain marine-derived isolates like S. bacillaris MBTG32, have also been reported to produce tunicamycin, though typically at lower levels.^[9]^[10] These organisms are cultivated through aerobic submerged fermentation in nutrient-rich media to induce tunicamycin biosynthesis. Typical media include tryptone-yeast extract-dextrose (TYD) formulations with 6 g/L glucose, 2 g/L yeast extract, 2 g/L tryptone, and 0.3 g/L MgCl₂·6H₂O, or variations with 1–6% carbohydrates (e.g., glucose or starch) and 0.2–6% nitrogen sources (e.g., yeast extract or soybean meal).^[11]^[9] Fermentation occurs at 28–30°C for 4–7 days under agitation (200–250 RPM) and aeration (0.25–1.0 vvm), with pH maintained at 6.0–8.0; production peaks intracellularly in the mycelia during the stationary phase.^[12]^[13] Industrial-scale production faces challenges such as low natural yields in wild-type strains, self-toxicity of tunicamycin to the producer, and difficulties in downstream recovery due to its association with biomass.^[14] Yield optimization techniques include medium engineering (e.g., adjusting carbon-to-nitrogen ratios with glucose and yeast extract for enhanced growth) and genetic modifications, such as heterologous expression of regulatory genes like pimM in S. clavuligerus, which can increase tunicamycin output up to fivefold.^[15]^[12] Further improvements involve strain selection via adaptive laboratory evolution to boost tolerance and productivity, though scalability remains limited by the antibiotic's instability and purification complexity.^[16]

Chemical Properties

Molecular Structure

Tunicamycin features a distinctive nucleoside core consisting of a uracil base N-glycosidically linked to a β-D-ribofuranose sugar at the 1' position, with the 5'-hydroxyl group of the ribose forming an α-glycosidic bond to the anomeric carbon (C1) of an N-acetyl-D-glucosamine (GlcNAc) unit. The anomeric carbon of this GlcNAc is simultaneously engaged in a β-glycosidic linkage to the anomeric carbon (C11) of the tunicamine moiety, creating a rare 1,1-disubstituted, trehalose-like glycosidic bond between the GlcNAc and tunicamine. The tunicamine unit is an unusual 11-carbon 2-amino-2,3-dideoxy-D-ribo-hexodialdose chain, characterized by an aldehyde at C1, a primary amine at C2 (N-acylated by the fatty acid), methylene at C3, hydroxyl groups at C4, C5, and C6, and the anomeric linkage at C11. This architecture positions key functional groups, including the uracil's carbonyls for hydrogen bonding, the GlcNAc's acetamido for polar interactions, and the lipophilic fatty acyl chain for membrane association.^[17] The natural isolate of tunicamycin exists as a homologous mixture, primarily variants A through E, distinguished by the length and branching of the fatty acyl chain attached via an amide bond to the 2-amino group of tunicamine. These homologues feature fatty acids ranging from C8 (straight-chain octanoyl in homolog A) to C17 (e.g., heptadecanoyl in homolog E), with predominant components B (C15, often 10-methylhexadecanoyl), C (C16, hexadecanoyl), and D (C17, anteiso-heptadecanoyl) accounting for most of the mixture. For instance, the major homolog C2 has the molecular formula C₃₉H₆₄N₄O₁₆ and a molecular weight of approximately 844.9 Da, while homolog A1 is C₃₇H₆₀N₄O₁₆ (816.9 Da).^[18] The stereochemistry of tunicamycin is precisely defined at multiple chiral centers, ensuring its biological specificity. The uridine portion exhibits standard β-D-ribofuranosyl configuration with (R) at C1', (S) at C2', (R) at C3', and (S) at C4'. The GlcNAc adopts the D-gluco configuration: (R) at C2, (S) at C3, (R) at C4, and (R) at C5, with the α-anomeric linkage to ribose and β to tunicamine. Tunicamine possesses the D-ribo-hexodialdose stereochemistry, featuring (S) at C2 (amino-bearing), (R) at C4, (S) at C5, and (R) at C6, with the β-anomeric configuration at C11 for the glycosidic bond to GlcNAc. These configurations were confirmed through degradative analysis and NMR studies in the original structural elucidation.

Physical and Chemical Characteristics

Tunicamycin is typically obtained as a white to off-white crystalline powder, facilitating its handling in laboratory settings.^[19]^[20] The compound exhibits limited solubility in water, with concentrations below 5 mg/mL even at pH 9, due to its amphiphilic nature from the lipophilic fatty acid chain. It dissolves more readily in organic solvents, achieving solubilities >10 mg/mL (up to 20 mg/mL) in DMSO, <5 mg/mL in methanol, approximately 1 mg/mL in ethanol, and over 10 mg/mL in DMF.^[19]^[21] Tunicamycin demonstrates sensitivity to acid hydrolysis and light exposure, which can degrade its structure, but it maintains stability under neutral to alkaline conditions and when stored at 2–8°C in the dark.^[22]^[21] Spectroscopic analysis reveals UV absorption maxima at 208 nm and 260 nm, primarily from the uracil moiety. The molecular weights of its homologs range from 817 Da (homolog A) to 859 Da (homolog D), reflecting variations in the fatty acid side chain length. For high-purity applications, the homologs can be effectively separated using reversed-phase high-performance liquid chromatography, enabling isolation of individual components with purities exceeding 98%.^[23]^[24]^[25]

Biosynthesis

Gene Cluster

The tun gene cluster responsible for tunicamycin biosynthesis in Streptomyces chartreusis was first identified in 2010 through genome sequencing and mining strategies applied to strain NRRL 12338. This cluster spans approximately 12 kb and encompasses 14 genes, designated tunA through tunN, which demonstrate a high degree of translational coupling to ensure efficient co-expression. Bioinformatic annotation revealed that these genes encode enzymes tailored for nucleoside antibiotic assembly, with bioinformatic and gene disruption studies identifying tunA, tunB, tunC, tunD, tunE, and tunH as essential for tunicamycin production, while tunF, tunG, tunK, tunL, and tunN enhance efficiency and flux.^[26] Among the key genes, tunA encodes an NAD-dependent epimerase/dehydratase that processes UDP-N-acetylglucosamine into an exo-glycal intermediate critical for the modified sugar component. tunD encodes a glycosyltransferase that establishes the unique α,β-1,1-glycosidic linkage in the disaccharide core. tunM encodes a radical S-adenosylmethionine (SAM) enzyme that, in cooperation with tunB, facilitates the C-C bond formation linking the uracil nucleoside to the sugar derivative. tunB encodes a radical SAM enzyme that likely generates a reactive uridine-5'-aldehyde or radical intermediate for this coupling. The cluster exhibits evolutionary adaptations, including Type I polyketide synthase (PKS)-like modules repurposed for nucleoside rather than polyketide chain elongation, highlighting a divergence in secondary metabolite pathways among actinomycetes. Its G+C content (65%) is notably lower than the host genome average (~72%), consistent with horizontal gene transfer events. Homologous clusters occur in other Streptomyces species, underscoring a conserved genomic architecture for tunicamycin production across select actinobacterial producers.

Biosynthetic Pathway

The biosynthesis of tunicamycin is a multi-step enzymatic process that assembles the antibiotic's unique structure from simple nucleotide sugar precursors, primarily UDP-N-acetylglucosamine (UDP-GlcNAc) and uridine triphosphate (UTP). The pathway, encoded by the tun gene cluster in producing actinomycetes such as Streptomyces chartreusis, proceeds through a linear sequence of transformations that build the undecose sugar chain, link it to the uracil nucleoside, and append a variable fatty acyl group, resulting in the final product's characteristic nucleoside-linked glycolipid architecture. This assembly highlights unusual biochemical strategies, including the formation of reactive exo-glycal intermediates, which enable the construction of the strained 11-carbon tunicamine moiety.^[27]^[28]^[26] The pathway initiates with TunA, a UDP-GlcNAc 5,6-dehydratase, which catalyzes the dehydration of UDP-GlcNAc to generate the key exo-glycal intermediate UDP-6-deoxy-GlcNAc-5,6-ene, thereby establishing the unsaturated undecose chain foundation essential for subsequent carbon-carbon bond formation. This step is critical, as TunA's activity creates a reactive enol ether that serves as the building block for the sugar's unusual stereochemistry and ring structure. Following dehydration, TunF, an epimerase homologous to UDP-glucose 4-epimerases, inverts the configuration at the C5' position of the exo-glycal, converting it to UDP-6-deoxy-GalNAc-5,6-ene and ensuring the correct galactosamine-like configuration in the tunicamine unit. These early modifications set the stage for core assembly, where enzymes such as TunB and TunM facilitate the attachment of the modified sugar to a uridine-derived moiety via radical-mediated C-C bond formation; TunB likely generates a uridine-5'-aldehyde or radical from UTP (possibly via phosphatase activity of TunG), enabling the coupling.^[27]^[28]^[27] The linear pathway continues with reduction and hydrolysis steps (involving TunD, TunE, and TunH) to yield the core UDP-N-acetyltunicaminyl-uracil intermediate, where TunD adds the N-acetylglucosamine unit, releasing the free anomeric hydroxyl at C11' of the sugar. Completion occurs through fatty acid acylation, where TunL, a phosphatase, works in concert with acyl carrier protein TunK and acyltransferase TunC to activate and transfer variable fatty acyl chains (typically 8-12 carbons, derived from β-oxidation or amino acid catabolism of valine, leucine, or isoleucine) onto the 11'-hydroxyl, introducing the structural diversity observed among tunicamycin homologs. This branched acylation step, mediated by the acyl carrier protein system, allows for homolog variation by incorporating different chain lengths and branching patterns from the cellular fatty acid pool, without altering the core nucleoside-sugar scaffold. The overall process exemplifies a modular yet tightly coordinated assembly, with non-essential accessory genes like tunF, tunG, and tunL enhancing flux and efficiency rather than being strictly required for core production.^[28]^[26]^[26]

Mechanism of Action

Inhibition of N-Linked Glycosylation

Tunicamycin specifically inhibits the enzyme UDP-N-acetylglucosamine—dolichyl-phosphate N-acetylglucosaminephosphotransferase, known as DPAGT1 in eukaryotes and GlcNAc-1-P transferase in prokaryotes, which catalyzes the committed first step in N-linked glycoprotein biosynthesis.^[29] This enzyme transfers N-acetylglucosamine-1-phosphate (GlcNAc-1-P) from the donor substrate UDP-N-acetylglucosamine (UDP-GlcNAc) to dolichol phosphate (Dol-P), forming GlcNAc-pyrophosphoryl-dolichol (GlcNAc-PP-Dol), an essential lipid-linked oligosaccharide precursor.^[30] The inhibited reaction is as follows:

\text{UDP-GlcNAc} + \text{Dol-P} \rightarrow \text{GlcNAc-PP-Dol} + \text{UMP}

By blocking this transfer, tunicamycin prevents the assembly of the full oligosaccharide precursor on the endoplasmic reticulum membrane, halting N-linked glycosylation.^[29] The binding mechanism of tunicamycin involves structural mimicry of the natural substrate UDP-GlcNAc, allowing it to act as a competitive inhibitor with high affinity (K_d ≈ 5.6 nM).^[29] Its uracil moiety mimics the uracil base of UDP, while the N-acetylglucosamine (GlcNAc) portion closely resembles the GlcNAc sugar of UDP-GlcNAc, enabling both components to occupy the enzyme's active site and form stabilizing interactions such as π-π stacking with residues like Phe249 and hydrogen bonds with Asp252 and Asn119.^[30] Additionally, tunicamycin's lipid chain partially mimics the dolichol phosphate acceptor, further competing at the active site and preventing the nucleophilic attack necessary for GlcNAc-1-P transfer.^[29] Crystal structures of DPAGT1 in complex with tunicamycin confirm this mimicry, revealing an enclosed binding pocket that traps the inhibitor and blocks substrate access.^[30] This inhibition is highly specific to N-linked glycosylation pathways, as tunicamycin targets the GlcNAc-1-P transferase family without affecting O-linked glycosylation, which relies on different enzymatic mechanisms.^[29] In eukaryotes, the selectivity for DPAGT1 underlies tunicamycin's utility in studying N-glycan-dependent processes, though it can also inhibit prokaryotic homologs like MraY involved in cell wall synthesis.^[30]

Downstream Cellular Effects

Tunicamycin's blockade of N-linked glycosylation causes the accumulation of unfolded or misfolded proteins within the endoplasmic reticulum (ER), as nascent polypeptides fail to receive proper glycan modifications essential for folding and quality control. This buildup activates the unfolded protein response (UPR), a conserved signaling cascade mediated by sensors such as PERK, IRE1, and ATF6, which initially aims to attenuate translation, enhance chaperone expression, and degrade aberrant proteins to restore ER homeostasis.^[31]^[32] However, persistent ER stress from tunicamycin overwhelms these adaptive mechanisms, leading to maladaptive outcomes including inflammation and cellular dysfunction across various cell types.^[33] The UPR triggered by tunicamycin also induces cell cycle arrest in the G1 phase, allowing cells time to repair damage before DNA replication. This halt stems from deficiencies in N-glycosylated proteins critical for G1/S transition, such as integrins involved in cell adhesion and signaling, and growth factor receptors that drive proliferation. In human and other mammalian cells, PERK-mediated phosphorylation of eIF2α contributes to this arrest by selectively repressing translation of cyclin D and other pro-progression factors.^[34]^[35]^[32] In mammalian cells, unresolved ER stress from tunicamycin escalates to apoptosis through the PERK-eIF2α-ATF4-CHOP pathway, where the transcription factor CHOP (also known as GADD153) upregulates pro-death genes like DR5 and BIM while downregulating anti-apoptotic Bcl-2 family members. This culminates in mitochondrial outer membrane permeabilization and caspase activation, with caspase-9 and caspase-3 executing the apoptotic program. Studies in diverse models, including neurons and cancer cells, confirm CHOP's pivotal role, as its knockdown attenuates tunicamycin-induced death.^[36]^[37]^[38] Beyond eukaryotic cells, tunicamycin exerts antibacterial effects primarily against Gram-positive bacteria by inhibiting MraY, a key enzyme in peptidoglycan biosynthesis that transfers phospho-MurNAc-pentapeptide to undecaprenyl phosphate to form lipid I. This disruption impairs cell wall cross-linking and integrity, leading to osmotic lysis and growth inhibition, as observed in species like Staphylococcus aureus and Bacillus subtilis. Tunicamycin shows greater activity against Gram-positive bacteria than Gram-negatives due to poor penetration of the outer membrane in the latter, which acts as a permeability barrier.^[39]^[40]

Biological Activities and Applications

Antibiotic Properties

Tunicamycin demonstrates potent antibiotic activity against Gram-positive bacteria, including species such as Bacillus subtilis and Staphylococcus aureus, as well as against fungi like Candida albicans and yeasts. It also exhibits strong activity against mycobacteria, such as Mycobacterium marinum, with a minimum inhibitory concentration (MIC) of 0.025 μg/mL.^[41]^[42]^[43]^[2] This narrow-spectrum profile arises from its targeted inhibition of key glycosylation steps in microbial cell wall biosynthesis, disrupting the formation of essential lipid-linked intermediates required for peptidoglycan and other surface structures.^[39]^[42] In contrast, tunicamycin exhibits no antibacterial activity against Gram-negative bacteria, such as Pseudomonas aeruginosa or Escherichia coli, primarily due to the impermeability of their outer membrane, which prevents the antibiotic from reaching its intracellular target.^[41]^[44] For sensitive Gram-positive strains and fungi, minimum inhibitory concentrations (MICs) generally fall within the range of 0.1–10 μg/mL, with examples including 0.1–3.13 μg/mL against various Bacillus strains and 2–32 μg/mL against C. albicans.^[45]^[42]^[43] Historically, despite its promising in vitro antimicrobial effects, tunicamycin was evaluated as a narrow-spectrum antibiotic but not advanced for clinical development owing to its high toxicity toward eukaryotic cells, which share similar glycosylation pathways.^[46]^[39] This limitation has confined its utility to laboratory research rather than therapeutic applications against microbial infections.^[46]

Research and Therapeutic Uses

Tunicamycin is widely employed in cell culture studies to induce endoplasmic reticulum (ER) stress, enabling researchers to investigate the unfolded protein response (UPR) and its implications in protein folding disorders.^[47] By inhibiting N-linked glycosylation, it triggers the accumulation of misfolded proteins in the ER, mimicking pathological conditions associated with neurodegenerative diseases such as Alzheimer's.^[48] For instance, in neuronal models, tunicamycin treatment has been used to replicate ER stress-mediated spatial memory deficits and amyloid-beta aggregation, providing insights into UPR activation pathways like PERK and IRE1.^[49] In cancer research, tunicamycin sensitizes multidrug-resistant cells to chemotherapy by exacerbating glycosylation defects and intensifying ER stress. Specifically, in gastric cancer models, it overcomes resistance to agents like cisplatin by upregulating UPR markers such as CHOP and GRP78, leading to enhanced apoptosis in resistant cell lines like SGC7901/ADR.^[50] This approach highlights its utility in studying how glycosylation inhibition disrupts tumor cell survival mechanisms without directly serving as an antibiotic. Recent advancements include the development of tunicamycin derivatives with reduced toxicity for therapeutic applications. The derivative TunR2, modified to minimize eukaryotic cell interference while retaining antibacterial potency, demonstrated efficacy in a 2024 zebrafish model of Mycobacterium marinum infection, a surrogate for tuberculosis, by clearing bacterial loads at doses that spared host viability. As of 2025, synthetic tunicamycin derivatives have been evaluated for activity against Mycobacterium avium complex, showing MICs in the range of 16–32 μg/mL against strains like M. avium subsp. paratuberculosis, with low cytotoxicity in bovine cells. Additionally, tunicamycin exhibits synergistic effects with β-lactam antibiotics possessing five-membered ring structures, enhancing activity against Gram-positive bacteria such as Staphylococcus aureus.^[51]^[52]^[53] Common experimental protocols involve dosing cells with 1–5 μg/mL tunicamycin for 24–48 hours to reliably induce ER stress in vitro, as this range activates UPR without excessive cytotoxicity in various mammalian cell lines.^[54]

Toxicity and Safety

Toxicity Mechanisms

Tunicamycin exerts its toxicity primarily through inhibition of N-linked glycosylation, resulting in the accumulation of unfolded or misfolded proteins within the endoplasmic reticulum (ER). This triggers ER stress overload, activating the unfolded protein response (UPR) as a cellular adaptive mechanism to restore homeostasis. However, prolonged exposure leads to chronic UPR activation, where the adaptive phase transitions to a pro-apoptotic state, characterized by upregulation of transcription factors like CHOP (C/EBP homologous protein), promoting cell death pathways.^[55]^[33] The chronic ER stress induced by tunicamycin disrupts calcium homeostasis, causing depletion of ER calcium stores and increased transfer of calcium to mitochondria via ER-mitochondria contact sites. This calcium dysregulation overloads mitochondrial calcium handling, leading to mitochondrial dysfunction, including impaired bioenergetics, reactive oxygen species production, and activation of mitophagy or apoptosis. These interconnected effects amplify cellular damage, contributing to the compound's overall toxicity profile.^[56]^[57] In mammals, tunicamycin's toxicity manifests as organ-specific effects, particularly hepatotoxicity and nephrotoxicity, due to impaired glycoprotein synthesis and function in metabolically active liver and kidney cells. In the liver, this results in steatosis, apoptosis, and lipid accumulation, while in the kidneys, it causes acute injury through similar ER stress-mediated pathways. The median lethal dose (LD50) in mice via intraperitoneal administration is approximately 2 mg/kg, with fatality at higher doses attributed to widespread systemic blockade of glycosylation and resultant multi-organ failure.^[55]^[58] Tunicamycin has no approved clinical use in humans due to its severe toxicity.^[55]

Safety Considerations

Tunicamycin is classified under the Globally Harmonized System (GHS) as an acute toxicity category 2 substance for oral exposure, with the hazard statement H300 indicating it is fatal if swallowed.^[59] It is also recognized as an irritant to skin and eyes, potentially causing redness, pain, or blurred vision upon contact.^[59]^[60] In laboratory settings, safe handling requires the use of personal protective equipment (PPE), including chemical-resistant gloves (such as nitrile rubber), safety glasses or goggles, and protective clothing to prevent skin and eye exposure.^[61]^[59] Operations should be performed in a well-ventilated fume hood to minimize inhalation of dust or aerosols, with strict protocols to avoid ingestion, such as prohibiting eating, drinking, or smoking in the work area and washing hands thoroughly after handling.^[61]^[59] If dust is generated, respiratory protection with a P3 filter is advised.^[61] For storage, tunicamycin should be kept at -20°C in tightly sealed, desiccated containers protected from light and moisture to preserve stability, offering a shelf life of 2–3 years under these conditions.^[62]^[63]^[64] Tunicamycin is designated exclusively as a research chemical and is not approved for therapeutic or commercial applications, with suppliers providing it under research use exemptions such as TSCA (40 CFR 720.36).^[61]^[60] Due to its antibiotic properties, its distribution and use are subject to general regulatory oversight on antimicrobials in various countries to address concerns over potential contributions to resistance development.^[61]

References

[1]
Tunicamycin: Uses, Interactions, Mechanism of Action - DrugBank
Apr 5, 2017 · Tunicamycin blocks N-linked glycosylation (N-glycans) resulting in cell cycle arrest at the G1 phase in human cells. It is used as an ...
[2]
The tunicamycin derivative TunR2 exhibits potent antibiotic ... - NIH
Jan 18, 2024 · Tunicamycins (TUN) are well-defined, Streptomyces-derived natural products that inhibit protein N-glycosylation in eukaryotes, ...Missing: sources | Show results with:sources
[3]
Analysis of the Tunicamycin Biosynthetic Gene Cluster of ...
The tunicamycin biosynthetic gene cluster of Streptomyces chartreusis consists of 14 genes (tunA to tunN) with a high degree of apparent translational ...
[4]
Biosynthesis of the Tunicamycins: A Review - Nature
Aug 1, 2007 · Tunicamycins are nucleotide sugar analogs produced by several Streptomyces species. In eukaryotes, tunicamycins inhibit ...
[5]
Tunicamycin specifically aggravates ER stress and overcomes ...
Nov 9, 2018 · Tunicamycin specifically aggravates ER stress and overcomes chemoresistance in multidrug-resistant gastric cancer cells by inhibiting N-glycosylation.
[6]
TUNICAMYCIN, A NEW ANTIBIOTIC. I - J-Stage
Tunicamycin is a new antiviral antibiotic produced by Streptomyces lysosuperificus, nov. sp. The active substance in culture broth is purified by solvent ...
[7]
The Structure of Tunicamycin - J-Stage
1) A. Takatsuki, K. Arima and G. Tamura, J. Antibiot., 24, 215 (1971). · 2) T. Ito, Y. Kodama, K. Kawamura, K. Suzuki, A. Takatsuki and G. Tamura, Agric. Biol.Missing: 1970s | Show results with:1970s
[8]
Tunicamycins from Marine-Derived Streptomyces bacillaris Inhibit ...
Jun 26, 2024 · Tunicamycins are a class of nucleoside sugar analog compounds that are characterized by the uracil moiety followed by an eleven-carbon dialdose ...
[9]
Genome Sequences of Three Tunicamycin-Producing Streptomyces ...
Tunicamycins are also produced by two strains of Streptomyces chartreusis (NRRL 3882 and NRRL 12338), Streptomyces clavuligerus NRRL 3585, Clavibacter toxicus ...Missing: organisms | Show results with:organisms
[10]
US4330624A - Process for producing Tunicamycin - Google Patents
The antibiotic Tunicamycin is produced by fermenting a Tunicamycin-producing strain of Streptomyces (Streptomyces griseus ATCC 31591) under controlled ...
[11]
Biosynthesis of Tunicamycin and Metabolic Origin of the 11-Carbon ...
Tunicamycin is a reversible inhibitor of polyprenol-phosphate: N-acetylhexosamine-1-phosphate translocases and is produced by several Streptomycesspecies.
[12]
U.S. Patent for Process for preparing tunicamycin Patent (Patent ...
Tunicamycin is produced by the cultivation of Streptomyces chartreusis Calhoun and Johnson, 1956, NRRL 12338. Methods of recovering tunicamycin and for ...
[13]
The secreted metabolome of Streptomyces chartreusis and ... - PNAS
Feb 20, 2018 · We characterized the secreted metabolome of the tunicamycin producer Streptomyces chartreusis NRRL 3882. The genome harbors 128 predicted biosynthetic gene ...
[14]
Activation of Secondary Metabolite Gene Clusters in Streptomyces ...
clavuligerus::pimM, and determined to be the result of a fivefold increase in the production of the tunicamycin complex. Introduction. PimM is a PAS-LuxR type ...
[15]
Exploiting Adaptive Laboratory Evolution of Streptomyces ...
We present a method here that, in contrast, exploits the power of adaptation among antibiotic producers to accelerate the discovery of antibiotics.
[16]
Tunicamycin – A powerfull mixture of homologous nucleoside ...
Feb 16, 2025 · Tunicamycin is a strong antibiotic that induces the unfolded protein response (UPR). This response activates during accumulation of unfolded or ...Missing: sources | Show results with:sources
[17]
Tunicamycin (3516) by Tocris, Part of Bio-Techne
Rating 5.0 (4) Tunicamycin contains four main components as follows: Homolog A, n=8, C37H60N4O16, molecular weight = 816.90. Homolog B, n=9, C38H62N4O16, molecular weight = ...Missing: structure | Show results with:structure
[18]
Tunicamycin from Streptomyces sp.; 11089-65-9 Sigma-Aldrich
### Summary of Tunicamycin Physical and Chemical Characteristics (T7765)
[19]
11089-65-9・Tunicamycin・202-08241・208 ... - FUJIFILM Wako
Tunicamycin ; Distributor: 208-08243 ; Barcode No: 4987481339828 ; Appearance, White - pale brown, powder ; Melting Point, 239 degrees C ; Specific Rotation, +52 ° ( ...<|separator|>
[20]
TUNICAMYCIN | 11089-65-9 - ChemicalBook
TUNICAMYCIN Properties ; 2-8°C · Soluble in methanol, ethanol, DMSO, or DMF · White to off-white solid · White · Streptomyces sp.
[21]
https://www.chemicalbook.com/ChemicalProductProperty_EN_CB4211576.htm
[22]
[PDF] PRODUCT INFORMATION - Caymanchem
UV/Vis.: λmax: 208, 260 nm. Supplied as: A crystalline solid. Storage: -20 ... The solubility of tunicamycin in these solvents is approximately. 20 mg/ml ...
[23]
Tunicamycin | Other Transferases | Tocris Bioscience
Rating 4.8 (4) · $45 deliveryBiological Activity for Tunicamycin Tunicamycin contains four main components as follows: Homolog A, n=8, C37H60N4O16, molecular weight = 816.90. Homolog B, n= ...Missing: physical properties stability UV
[24]
Separation of tunicamycin homologues by reversed-phase high ...
Separation of tunicamycin homologues by reversed-phase high-performance liquid chromatography.Missing: HPLC | Show results with:HPLC
[25]
https://pubmed.ncbi.nlm.nih.gov/7440684/
[26]
https://doi.org/10.1128/AAC.00130-18
[27]
https://doi.org/10.1038/nchem.1351
[28]
GlcNAc-1-P-transferase-tunicamycin complex structure reveals ...
Here we present crystal structures of human GPT in complex with tunicamycin. Our structural and functional analyses reveal the difference between GPT and MraY.Missing: trehalose | Show results with:trehalose
[29]
Structures of DPAGT1 Explain Glycosylation Disease Mechanisms ...
Nov 1, 2018 · The effects of addition of the substrates Dol-P and UDP-GlcNAc, and the inhibitor tunicamycin on thermostability of DPAGT1 were also tested (n=9) ...
[30]
Tunicamycin induced endoplasmic reticulum stress promotes ... - NIH
Our data demonstrate that tunicamycin induced ER stress promotes prostate cancer cell death by activating mTORC1 through eNOS-RagC pathway.Missing: hydrolysis | Show results with:hydrolysis
[31]
PERK and GCN2 Contribute to eIF2α Phosphorylation and Cell ...
Sep 21, 2005 · Arrest in G1 phase in response to ER stress is thought to provide the cell an opportunity to restore cellular homeostasis before committing to ...
[32]
Endoplasmic reticulum stress: molecular mechanism and ... - Nature
Sep 15, 2023 · Under prolonged ER stress, three branches of UPR are activated, which leads to cell death via a complex consisting of pro-caspase-8 and fas- ...
[33]
Analysis of the Protein Glycosylation Defect of a ... - PubMed - NIH
A temperature-sensitive mutant with a defect in glycoprotein synthesis and a cell cycle (G1)-specific arrest at the nonpermissive temperature (Tenner et al., J.Missing: deficiencies | Show results with:deficiencies
[34]
N-glycans in cell survival and death: Cross-talk between ... - NIH
Tunicamycin treatment arrests capillary endothelial cells in G1 and induces programmed cell death. ... Glycosylation: interplay between dolichol cycle and cell ...
[35]
Tunicamycin Enhances Tumor Necrosis Factor–Related Apoptosis ...
Jul 15, 2005 · Of note, tunicamycin-mediated induction of CHOP and DR5 protein expression was not observed in normal human peripheral blood mononuclear cells.
[36]
Gene expression during ER stress–induced apoptosis in neurons
Aug 11, 2003 · Tunicamycin treatment also led to activation of caspase-9, the apical caspase in the mitochondrial apoptosis pathway (Fig. 6 C). Subsequently, ...
[37]
Neuronal Apoptosis Induced by Endoplasmic Reticulum Stress Is ...
Dec 15, 2010 · Together, our results indicate that ER stress induces neuronal apoptosis through a p53-independent pathway involving ATF4- and CHOP-mediated ...<|separator|>
[38]
Exploring the Active Site of the Antibacterial Target MraY by ...
Nov 9, 2020 · In this work, we have used tunicamycin and modified versions of tunicamycin as tool compounds to explore the active site of MraY and to gain further insight ...<|separator|>
[39]
Structural basis for selective inhibition of antibacterial target MraY, a ...
Through inhibition of MraY, tunicamycin can block cell wall synthesis in Gram-positive bacteria 28, 35, but is not active against Gram-negative bacteria ...
[40]
TUNiCAMYCIN, A NEW ANTIBIOTIC. I ISOLATION AND ... - J-Stage
Tunicamycin was active against Gram- positive bacteria, yeasts and fungi. Bacillus species were the most sensitive to the antibiotic among all examined.
[41]
Tunicamycin Mediated Inhibition of Wall Teichoic Acid Affects ...
Tunicamycin inhibits wall teichoic acid (WTA), an important cell wall molecule in Gram-positive bacteria that plays a major role in physiology and pathogenesis.
[42]
Antimicrobial tunicamycin derivatives from the deep ... - ResearchGate
albicans CMCC (F) 98001 with MIC values ranging from 2 to 32 μg/mL. This is the first report that tunicamycins exhibit antimicrobial activities against B.
[43]
Tunicamycins from Marine-Derived Streptomyces bacillaris Inhibit ...
Jun 26, 2024 · However, these compounds showed weak or no activities against Gram-negative bacteria. Based on the reported data, compounds 1–4 were further ...
[44]
MraY: An Emerging Therapeutic Target in Bacterial Peptidoglycan ...
Oct 10, 2025 · ... MIC values of 0.1-3.13 μg/mL against various strains of P. ... Tunicamycin showed potency against Gram-positive bacteria, mostly Bacillus ...
[45]
Tunicamycin - an overview | ScienceDirect Topics
Tunicamycin, a naturally occurring antibiotic, is a well-established ER stress inducer acting via inhibition of protein N-linked glycosylation.
[46]
Tunicamycin-induced Unfolded Protein Response in the Developing ...
Tunicamycin inhibits protein glycosylation and is a commonly used ER stress inducer. In this study, we injected tunicamycin subcutaneously on the back of mouse ...
[47]
Model Identifies Genetic Predisposition of Alzheimer's Disease as ...
To mimic additional environmental stress, cells were treated with 1 µg/mL of tunicamycin (Tm), a well-characterized ER stress inducer that inhibits protein ...<|separator|>
[48]
Endoplasmic reticulum stress induces spatial memory deficits by ...
Here, we injected tunicamycin (TM), a recognized ER stress inducer, into the brain ventricle of Sprague‐Dawley (SD) rats to induce the unfolded protein ...
[49]
Tunicamycin specifically aggravates ER stress and overcomes ...
Nov 9, 2018 · Tunicamycin specifically aggravates ER stress and overcomes chemoresistance in multidrug-resistant gastric cancer cells by inhibiting N- ...Missing: defects | Show results with:defects
[50]
The tunicamycin derivative TunR2 exhibits potent antibiotic ...
The tunicamycin derivative TunR2 exhibits potent antibiotic properties with low toxicity in an in vivo Mycobacterium marinum-zebrafish TB infection model. J ...Missing: paper | Show results with:paper
[51]
Tunicamycin-induced ER stress in breast cancer cells neither ...
There was ~33% reduction in cell proliferation in 24 h at tunicamycin concentration of 1.0 μg/mL (Figure 2). ... tunicamycin (1 μg/mL) for 48 h. Top: GRP78 ...
[52]
Role of endoplasmic reticulum stress in drug‐induced toxicity
Feb 4, 2016 · We also included data on tunicamycin (an antibiotic not used in human medicine because of its toxicity) and thapsigargin (a toxic compound ...
[53]
mTORC1 inhibitor rapamycin and ER stressor tunicamycin induce ...
Nov 3, 2016 · In a previous study with HeLa cells, we showed that ER-to-mitochondria Ca2+ transfer increases during the early phase of ER stress induced by ...
[54]
Tunicamycin-Induced Endoplasmic Reticulum Stress Damages ...
Aug 9, 2022 · ER stress occurs in many pathological conditions including aging [28,29,30], diabetic disease [24], doxorubicin cardiotoxicity [31], and heart ...Missing: UPR dysregulation
[55]
Tunicamycin enhances the antitumor activity of trastuzumab on ...
Nov 17, 2015 · Tunicamycin, an inhibitor of N-glycosylation, synergistically enhanced the antitumor activity of trastuzumab against HER2-overexpressing breast cancer cells.<|control11|><|separator|>
[56]
None
**Summary of Tunicamycin Safety Data Sheet (Tocris Bioscience SDS)**
[57]
None
**Summary of Tunicamycin Safety Data Sheet (MP Biomedicals SDS)**
[58]
None
**Summary of Sigma-Aldrich SDS for Tunicamycin (T7765)**
[59]
https://documents.tocris.com/pdfs/tocris_msds/3516_sds.pdf
[60]
Tunicamycin | ER stress inducer - Focus Biomolecules
The structure shown is for tunicamycin B (the C15 homolog). Tunicamycin is a potent inhibitor of GlcNAc phosphotransferase which thereby inhibits glycoprotein ...Missing: stereochemistry | Show results with:stereochemistry
[61]
https://www.sigmaaldrich.com/US/en/sds/sigma/t7765