Fts-Z Inhibition: Comparison
Please note this is a comparison between Version 2 by Catherine Yang and Version 1 by Abhishek Chauhan.

Fts-Z is being explored as potent target for inhibiting emerging microbes due to its central role in Z-ring formation and conserved nature in nearly all bacterial species and absence in higher eukaryotes. Its absence in bacteria induces filamentation and cell death occurs. Antimicrobial resistance (AMR) is a pressing issue worldwide that must be addressed swiftly. It is driven by spontaneous evolution, bacterial mutation, and the dissemination of resistant genes via horizontal gene transfer. Researchers are working on many novel targets, which can become a pathway to inhibit harmful bacteria. Filamentous Thermosensitive mutant-Z (Fts-Z) is one such bacterial target that has gained popularity amongst scientists due to its conserved nature in bacteria and absence in eukaryotes.

  • antimicrobials
  • cytokinesis
  • Fts-Z

1. Berberine and Derivatives

Berberine (IUPAC: 16,17-dimethoxy-5,7-dioxa-13-azoniapentacy-clo [,10.04,8.015,20] henicosa-1(13),2,4(8),9,14,16,18,20-octaene), a benzyl isoquinoline alkaloid (Figure 51) from the Berberis plant, show a mild antibacterial activity and Fts- Z inhibition. Sun et al. in their work, studied the active site in S. aureus for Fts-Z (PDB ID—4DXD) binding through in-silico technique and the found interdomain region participating actively in the docking comparable to that of PC190723 [61][1]. The planar structure of the compound is best suited for interaction with the C-terminus beta sheet of Fts-Z protein. Further they designed and synthesized 9-phenoxyalkyl substituted derivatives of berberine (Figure 62) and found a compound that has a high potent activity which was further verified through in-vitro antimicrobial susceptibility assay and GTPase activity assay. Dasgupta and colleagues, a few years earlier had reported the inhibitory activity of berberine through In-vitro isothermal colorimetry (ITC) and STD NMR spectroscopy [75][2]. The studies indicated the overlap of the binding site of berberine with the GTP binding pocket in the Fts-Z protein. Berberine also had low toxicity rates and some other side effects like that of bilirubin -induced brain damage causing jaundice in infants and expecting mothers [87,96,97][3][4][5].
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Figure 51. Berberine structure; Mol. Formula—C20H18NO4+; Mol. Wt.—336.4; Experimental details—berberine-dependent Fts-Z assembly observed (IC50 = 10.0 ± 2.5 µM); Fts-Z GTPase activity observed (IC50 = 16.01 ± 5.0 µM), ITC results—dissociation constant (KD = 0.023) entropy driven [61][1]. Source: PubChem-CID 2353.
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Figure 62. Berberine chloride derivative; Mol. Formula—C20H18ClNO4; Mol. Wt.—371.8; Experimental details—Inhibited MRSA ATCC 29247 (MIC = 2 µg mL−1), ATCC 700221 (MIC = 4 µg mL−1), E. coli (MIC = 32 µg mL−1), K. pneumoniae (MIC = 64 µg mL−1); showed GTPase (IC50 between 37.8 and 63.7 µM). In-silico studies done on PDB-4DXD (interacting residues were Ile197, Leu200, Val203, Leu209, Met226, Leu261, Val297 and Ile311) [61][1]. Source: PubChem-CID 12456.

2. Sanguinarine

Sanguinarine (IUPAC: 24-methyl-5,7,18,20-tetraoxa-24-azoniahexacy-clo [,10.04,8.014,22.017,21] tetracosa-1(24),2,4(8),9,11,13,15,17(21),22-nonaene) is a benzophenanthridine alkaloid from rhizome of Sanguinaria canadensis is found to inhibit cytokinesis in bacteria. It inhibits the E. coli Fts-Z assembly by perturbing the Z ring and was also found to inhibit B. subtilis cell growth without affecting nucleoid segregation at an IC50 of 3µM. This interaction was investigated through in-vitro size exclusion chromatography and fluoroscent probing. Mutational studies were also conducted by the group (Figure 73A) [90][6]. A representative compound 21 had 2 fold higher GTPase activity as compared to sanguinarine for which a patent was also filed [98][7]. Liu and coworkers designed and synthesized sequence of novel 5-methyl-2-phenylphenanthridium (Figure 73B) derivatives by simplifying the skeleton of sanguinarine. These had an exceptionally elevated anti-bacterial activity against an array of 10 antibiotic sensitive and resistant strains. MIC values for S. aureus ATCC25923, S. epidermisS. pyogenes PS and PRB. subtilis ATCC9372, B. pumilus ATCC63202 were ranged from 0.06 to 8 and 0.25–16 µg mL−1 respectively and for E. coli ATCC 25922 and P. aeruginosa ATCC27853 it was more than 64 µg mL−1 [89][8].
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Figure 73. (A) Sanguinarine; Mol. Formula—C20H14NO4+; Mol. Wt.—332.3; Experimental details—Dissociation constant (KD) = 18–20 µM; IC50 = 3 ± 1 µM for B. subtilis 168, 14 ± 2.3 µM for E. coli BL21 [89][8]. (B) 5-methyl-2-phenylphenanthridium derivative of Sanguinarine [97][5]. Source: PubChem-CID 5154; PMID-29657101.

3. Cinnamaldehyde and Derivatives

Cinnamaldehyde (IUPAC: (E)-3-phenylprop-2-enal), (Figure 84) a plant derived product from spices (stem bark of Cinnamomum cassia) has shown an array of potential medicinal properties. It has been reported to possess inhibitory activity against yeasts, filamentous molds and many bacteria through various pathways including inhibition of cell wall biosynthesis, changing of membrane structure and integrity and inhibiting GTPase activity [63][9]. Domadia and coworkers reported in-vitro, in-silico and in-vivo activity of cinnamaldehyde to perturb Z ring morphology and GTP hydrolysis with an affinity of 1.0 ± 0.2 µ/M [76][10]. Molecular modeling results were in concordance with STD-NMR results showing binding at the T7 loop in the C-terminal region. The results of MSA (multiple sequence alignment) also showed some of the residues- R202, V208, N263, G295, N263 to be highly conserved among Fts-Z. Xin and coworkers worked on derivatives of cinnamaldehyde where they found that substitution in the benzene ring at ortho or para position of cinnamaldehyde, by small groups increased the activity of compounds so synthesized against different microbes. They further stated that 2-methyl benzimidazoyl moiety was had a better efficiency against all strains, they tested and gave three compounds (marked as 3, 8, 10 in [94][11]) which had MIC of 4 µg mL−1 in two compounds and 10 µg mL−1 against S. aureus (ATCC 25923). Two compounds (marked as 4, 10 in [64][12]) gave MIC (4 µg mL−1)values 32 times better than the reference drugs used.
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Figure 84. Cinnamaldehyde structure. Mol. Formula—C9H8O; Mol. Wt.—132.16; Experimental details—inhibits E. coli (MIC = 1000 mgL−1), B. subtilis (MIC = 500 mgL−1), MSRA (MIC = 250 mgL−1), GTPase inhibition (IC50 = 5.81 ± 2.2 µM). In-silico docking (PDB ID—1FSZ), interacting residue were V208, R202, N263, G295, S297 [89][8]. Source PubChem: CID 637511.
In 2015, another group of researchers took this study one step further by synthesizing cinnamaldehyde derivatives and reported comparable activity of them wherein some possessed cell division inhibition properties in S. aureus between 0.25–4 µg mL−1. They found good activity when 2-methylbenzimidazolyl substitution was at the first position and 2,4-dichlorophenyl was at the third position. Polymerization inhibition and GTPase activity of S. aureus Fts-Z were shown in dose-dependent manner through biological assays of compounds [94][11].

4. Chrysophaentins

Chrysophaentins are group of anti-infectives obtained from marine sources, chrysophyte alga, Chryosphaeum taylori, including 8 phytochemicals (A-H), showed the inhibitory activity for MRSA, VREF (vancomycin-resistant E. faecium) and S. aureus [93][13]. Of these, Chrysophaentin A (IUPAC: (9E,25E)-4,10,20,26-tetrachloro-2,18-dioxapentacy-clo [2,7.119,23.012,17]tetratriaconta-1(30),3,5,7(34),9,12(17),13,15,19,21,23(33),25,28,31-tetradecaene-6,14,16,22,30,31-hexol), (Figure 95) showed the most potent antibacterial activity and also inhibited GTPase activity in E. coli which was attributed to the presence of hydroxyl group. Also, Chrysophaentins A had 12-fold higher MIC50 as compared to Chrysophaentins D, due to the presence of chlorine at chains A and C. Another compound hemi-Chrysophaentins(Figure 106) was synthesized and reported to have a reaction system of Chrysophaentins A [67][14].
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Figure 95. Chrysophaentin A Structure. Mol. Formula—C32H24Cl4O8; Mol. Wt.—678.3; Experimental details—GTPase activity (IC50 = 6.7 ± 1.7 µg mL−1); MIC50 = 1.8 ± 0.6 µg mL−1, 1.5 ± 0.7 µg mL−1, and 1.3 ± 0.4 µg mL−1 against SA, MRSA, and multi drug resistant SA (MDR-SA), respectively; and 3.8 ± 1.9 µg mL−1 and 2.9 ± 0.8 µg mL−1 toward E. faecium and VREF; In-silico docking on homology modelled E.coli, placed compound in GTP binding site (residues Gly20, Asn24, Asn 43, Ala 70, Thr 108, Arg 142 formed H-bond) [93][13]. Source: PubChem-CID 46872004.
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Figure 106. Hemichrysophaentin Structure; Mol. Formula—C18H18Cl2O4; Mol. Wt.—369.2 [93][13]. Source: PubChem-60164930.

5. Coumarins

Coumarins (IUPAC: chromen-2-one), (Figure 117) are 1,2-benzopyrone derivatives were derived from different plants with a proven Fts-Z inhibition activity. They have a 2H-chromen-2-one composed of lactone and aromatic ring, along with 2 oxygen atoms forming bonds with enzyme residues and thus are responsible for pharmacological properties. The aromatic ring also plays role in destabilizing enzymes by forming hydrophobic bonds [69][15]. Ammoresinol, anthogenol, ostruthin, novobiocin, chartreusin and coumermycin are some of the coumarins which also show anti-bacterial activity against many Gram-negative and Gram-positive bacteria [99][16]. A study suggested that coumarins had potent activity against M. tuberculosis (H37Rv) by inhibiting GTPase activity and polymerization of Fts-Z. Other coumarins namely, Scopoletin (having IC50 of 41 μM for Fts-Z polymerization and 23 μM for GTPase activity) and Daphnetin (IC50 of 73 μM for Fts-Z polymerization and 57 μM for GTPase activity) have proven activity. In-silico studies performed on coumarins and Fts-Z indicate that it binds in the T7 loop of Fts-Z [100,101,102,103,104,105,106][17][18][19][20][21][22][23].
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Figure 117. Coumarin Structure. Mol. Formula—C9H6O2; Mol. Wt.—146.14; GTPase activity (IC50 = 212 ± 4.12 µM); Fts-Z polymerization (IC50 = 200 ± 4.2 µM) [58][24]. Source: PubChem-323.

4.6. Curcumin

Curcumin (IUPAC: 1,7-bis(4-hydroxy-3-methoxyphenyl)-1,6-heptadiene-3,5-dione/diferuloyl methane), (Figure 128) is a chromophore in rhizomes of the plant Curcuma longa (turmeric). It is a polyphenolic compound, possessing a wide spectrum of biological activities and is traditionally used in as a household remedy for curing various diseases, as spice and as a food preservative in South East Asian countries including India [88][25]. The presence of two ortho methoxylated phenols having conjugate linking with beta-di-ketone function makes it an appealing target for the drug industry. Rai and coworkers, revealed the inhibitory action of curcumin to polymerize Fts-Z in B. subtilis wherein Z-ring formation was perturbed and GTPase activity was enhanced [107][26]. Roy and colleagues found putative curcumin binding sites in E. coli Fts-Z and B. subtilis Fts-Z forming bonds in the GTP binding pocket through the computational docking technique [108][27]. Some of the research groups are working on the nano-formulation of curcumin to increase its stability in in-vitro and in-vivo setups. The major drawback of curcumin is its poor aqueous solubility and bioavailability [92][28].
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Figure 128. Curcumin Structure; Mol. Formula—C21H20O6; Mol. Wt.—368.4; Experimental details—inhibited B. subtilis 168 (IC50 = 17 ± 3 µM), E. coli K12 MG1655 (IC50 = 58 ± 5 µM); dissociation constant (KD) = 7.3 ± 1.8 µM [108][27]. Source: PubChem-CID 969516.

7. Dichamanetin and Derivatives

Dichamanetin (Figure 139A) is a natural polyphenolic compound obtained/isolated from Uvariachamae and 2‴-hydroxy-5″-benxzylisouvarinol-B (Figure 139B) is another natural polyphenolic compound from Xylopia afticana found by two independent researchers [109][29]. Dichamanetin and derivatives are structurally similar to Zantrins Z1, and have anti-bacterial activity against many Gram-positive microbes (S. aureusB. subtilisM. smegmatis and E. coli) comparable to Zantrin. Urgaonkar and colleagues examined the impact of dichamanetin on E. coli Fts-Z GTPase activity and found that the inhibition IC50 values were 12.5 µM and 8.3 µM, respectively [109][29].
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Figure 139. (A) Dichamanetin Structure; Mol. Formula—C29H24O6; Mol. Wt.—468.5; Experimental details—GTPase inhibition in E.coli (IC50 = 12.5 ± 0.5 µM) [109][29]. (B) 2‴-hydroxy-5″-benxzylisouvarinol-B [109][29]. Source: PubChem-CID 181193.

8. Doxorubicin

Doxorubicin, (IUPAC: (7S,9S)-7-[(2R,4S,5S,6S)-4-amino-5-hydroxy-6-methyloxan-2-yl]oxy-6,9,11-trihydroxy-9-(2-hydroxyacetyl)-4-methoxy-8,10-dihydro-7H-tetracene-5,12-dione) (Figure 140) an anthracycline antibiotic derived from the actinobacterium Streptomyces peucetius, has been found as a powerful Fts-Z inhibitor that inhibits E. coli growth by disrupting Fts-Z functions [110][30]. It was identified as a small molecule targeting Fts-Z and suppressing bacterial division utilizing an independent computational, biochemical, and microbiological method from a drug library authorized by the US FDA. The fluorescence-binding experiment indicated that it interacts significantly with Fts-Z without changing membrane structure or nucleoid segregation in microbes. The effects were visible on both GTPase activity and Fts-Z assembly.
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Figure 140. Structure of Doxorubicin; Mol. Formula—C27H29NO11; Mol. Wt.—543.5; Experimental details—Antibacterial activity against E. coli BL21, B. subtilis (MIC—20 µM, 10 µM respectively); Dissociation constant (KD 120 ± 61 nM) [110][30]. Source: PubChem-CID 31703.

9. Phenylpropanoids

Phenylpropanoids are phytochemicals produced primarily due to stress including wounding, UV irradiation, pollutants, infections, and several other environmental factors to protect them against pathogens and predators. This defensive characteristic can be attributed to their free radical hunting and antioxidant properties [111][31]. Studies clearly indicate the use of these phytochemicals for the production of anti-bacterial agents [111][31]. Hemaiswarya and coworkers studied the effect of 8 phenylpropanoids (chlorogenic acid, caffeic acid, 2,4,5-trimethoxycinnamic acid, cinnamic acid and p-coumaric acid) (Figure 151A–E), against E. coli Fts-Z through both in-silico and in-vitro techniques [111][31]. Among them chlorogenic acid which is an ester of quinic aid and caffeic acid was found to have the highest IC50 value of 69.55 ± 3.6 µM, caffeic acid, cinnamic acid, p-coumaric acid followed with 105.96 ± 6.3 µM, 238.91 ± 7.1 µM, 189.53 ± 3.7 µM, respectively. 2,4,5-trimethoxy cinnamic acid, 3,4-dimethoxy cinnamic acid and eugenol were the least potent (IC50 < 250 µM.). Light scattering experiments and circular dichroism studies supported the results. The in-silico studies indicated that the binding of phenylpropanoids happens not less than a residue in the T7 loop which is considered to be most important in the Fts-Z structure. Some other compounds which have inhibitory effects against Fts-Z were phenyl acrylamide [111[31][32],112], vanillin derivative 3a and 4u which have been tested against S. aureus, S. pyogenes and M. tuberculosis [112,113,114][32][33][34]
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Figure 115. Phenylpropanoids group inhibiting Fts-Z: (A) Chlorogenic acid; (B) p-Coumaric acid; (C) Caffeic acid; (D) 2,4,5-Trimethoxycinnamic acid.; (E) Cinnamic acid. Source: PubChem.

10. Plumbagin

Plumbagin (IUPAC: 5-hydroxy-2-methylnaphthalene-1,4-dione), (Figure 162) is a phytochemical from the roots of the Plumbago zeylanica plant [90][6]. It is a secondary naphthoquinone derivative known to exhibit a variety of biological activities such as cell proliferation in mammals [115][35], fungus [116][36] and bacterial cells [117][37]. The antimicrobial properties do not affect E.coliS. typhimurium [118][38]. Acharya and coworkers, through their ex-vivo experiment demonstrated the binding of plumbagin with cellular microtubules in the colchicine cavity, cell viability experiments gave the IC50 value of 14.6 µm [119][39]. The structural similarity of Fts-Z with that of tubulin has caused many scientists to work on this and plumbagin was found to inhibit Fts-Z in B. subtilis 168 in a dose dependent manner. Further in-silico studies showed the possible binding site located at residues D199 and V307 [120][40].
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Figure 162. Plumbagin Structure. Mol. Formula—C11H8O3; Mol. Wt.—188.18; Dissociation constant (KD) 20.7 ± 5.6 µM [115][35]. Source: PubChem-10205.

11. Totarol

Totarol, a diterpene phenolic phytocompound, (IUPAC: (4bS,8aS)-4b,8,8-trimethyl-1-propan-2-yl-5,6,7,8a,9,10-hexahydrophenanthren-2-ol) (Figure 173), is obtained from a conifer (Podocarpus totara) and showed activity against M. tuberculosis and B. subtilis [121,122][41][42]. Although totarol was shown to have high anti-bacterial action against a variety of Gram-positive bacteria, it had no effect on Gram-negative bacteria and no antifungal properties as well. The experiments done indicated that totarol did not disrupt the B. subtilis membrane or nucleoid segregation, it only affected the functioning of the Z-ring.
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Figure 173. Totarol structure, Mol. Formula—C20H30O; Mol. Wt.—286.5; Experimental Details—MIC against B. subtilis = 2 µM, S. aureus = 5.4 µM, M. tuberculosis = 16 µg mL−1; Dissociation constant KD = 11 ± 2.3 µM [121][41]. Source: PubChem-CID 92783.

12. Viriditoxin

Viriditoxin (IUPAC: methyl 2-[(3S)-6-[(3S)-9,10-dihydroxy-7-methoxy-3-(2-methoxy-2-oxoethyl)-1-oxo-3,4-dihydrobenzo[g]isochromen-6-yl]-9,10-dihydroxy-7-methoxy-1-oxo-3,4-dihydrobenzo[g]isochromen-3-yl]acetate), (Figure 184) a cytotoxic compound obtained from fungus Aspergillus sp. (MF6890) was found to inhibit the bacterial Fts-Z polymerization by Wang and co-workers in 2003 [14][43]. The IC50 values for E. coli GTPase activity were 7.0 µg mL−1, for polymerization were 8.2 µg mL−1 and found to elongate B. subtilis cells. Another group of researchers isolated this compound from the fungus Paecilomyces variotii derived from jellyfish and found that viriditoxin stabilized microtubule polymers in SK-OV-3 cells and exhibited antimitotic and antimetastatic potential.
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Figure 184. Viriditoxin Structure. Mol. Formula—C34H30O14; Mol. Wt.—662.6; inhibited Fts-Z polymerization (IC50 = 8.2 μgmL−1), GTPase inhibition (IC50 = 7.0 μgmL−1) [14][43]. Source: PubChem-53343291.
Viriditoxin is also effective against a wide range of drug-resistant Gram-positive infections, including S. aureus (MIC 4–8 µg mL−1), and E. faecium (MIC 2–16 µg mL−1). Inducing Fts-Z expression in bacterial cells may increase the MIC value, suggesting that viriditoxin targets Fts-Z in these bacterial strains. Viriditoxin can induce B. subtilis cells to elongate, according to morphological research [94][11].


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