Open access peer-reviewed chapter

Photodynamic Inactivation of Escherichia coli with Cationic Porphyrin Sensitizers

By Jin Matsumoto, Tomoko Matsumoto, Kazuya Yasuda and Masahide Yasuda

Submitted: July 27th 2018Reviewed: November 21st 2018Published: December 28th 2018

DOI: 10.5772/intechopen.82645

Downloaded: 233

Abstract

The activity of singlet-oxygen sensitizers for photodynamic inactivation (PDI) of microorganisms and photodynamic therapy of tumor cells has been evaluated using Escherichia coli, Saccharomyces cerevisiae, and human cancer cell lines. In this chapter, drug resistance of E. coli was examined based on the PDI activity of a variety of RPy-P-porphyrin sensitizers with different number of ionic valence and different hydrophobic characters. The PDI activities toward E. coli were evaluated using the minimum effective concentrations ([P]) of the porphyrin sensitizers. It was found that the [P] value for E. coli was larger than that for S. cerevisiae. E. coli has drug-resistance toward hydrophobic and mono-cationic porphyrins. However, E. coli has weak drug-resistance toward the porphyrins with both polycationic character and hydrophobicity. Since the outer membrane mainly consists of lipopolysaccharides and phospholipids that are negatively charged, cationic porphyrins are able to adsorb to the outer leaflet. Then the cationic porphyrins with hydrophobic character can interact with not only the outer leaflet but also inner leaflet of the outer membrane and the plasma membrane. Thus, porphyrins may be incorporated inside E. coli cells via the self-promoted uptake pathway. Moreover, polycationic porphyrins can interact with DNA and proteins by strong binding affinities.

Keywords

  • PDT sensitizer
  • singlet oxygen
  • porphyrins
  • PDI activity
  • Escherichia coli
  • Saccharomyces cerevisiae

1. Introduction

Singlet-oxygen (1O2) sensitizers for photodynamic inactivation (PDI) of microorganisms and photodynamic therapy of tumor cells have been developed using Escherichia coli, Saccharomyces cerevisiae, and human cancer cell lines (e.g., HeLa cell) as model cells [1, 2, 3, 4]. As E. coli is a Gram-negative bacterium, the cell wall consists of an inner membrane, cytoplasmic membrane, a periplasmic space with a peptidoglycan layer, and an outer membrane [5]. Since the E. coli cell wall has a low permeability, there are only a few 1O2-sensitizers that can permeate the cell wall and inactivate E. coli efficiently at low concentrations.

PDI refers to the use of a visible-light source, oxidizing agents (e.g., O2), and photosensitizers. Photosensitizers absorb light energy that causes an energy transfer to O2, which leads to the formation of reactive oxygen such as 1O2, thereby inactivating cells and bacteria. Preliminary studies on the photodynamic action for biological systems started in the 1930s by PDI of phages using methylene blue [6, 7]. PDI of bacteria has received considerable attention as a methodology leading to the medical application of infection therapy beyond antimicrobial resistance. Among the large variety of photosensitizers developed for PDI over the last 60 years, porphyrins and metalloporphyrins became attractive sensitizers owing to their strong absorption band in the visible-light region [8, 9, 10, 11].

In the case of porphyrin sensitizers, their solubilities in water are an important characteristic for handling them as aqueous solutions, since porphyrin derivatives, in general, are poorly soluble in water. The most popular method to improve the solubility in water is the introduction of ionic groups to the porphyrin ring. Especially, the introduction of an alkylpyridinium (RPy) group into porphyrins is a useful method to make porphyrins water-soluble [12, 13]. A typical RPy-bonded porphyrin is represented by meso-tetra[4-(1-methyl-pyridinium)] porphyrin (TMP). The first application of TMP to PDI was reported by Ben Amor et al. in 1998 [14]. For the last two decades, a variety of RPy-bonded porphyrins have been prepared and studied for PDI [15, 16, 17, 18, 19, 20, 21].

We have interested in axially RPy-bonded tricationic P-porphyrins and their PDI activity [22, 23, 24, 25, 26]. It is advantageous that the water solubilization is easily achieved through the modification of the axial ligands of P-porphyrins. It is expected that polycationic porphyrins have strong binding affinities to DNA [27, 28, 29, 30, 31, 32]. In this chapter, drug resistance of E. coli was discussed based on PDI activity of a variety of P- and Sb-porphyrin sensitizers with different number of ionic valence and different hydrophobic character. The typical structure of the porphyrin sensitizer is shown in Figure 1, and they are named P-type porphyrin.

Figure 1.

Typical structure of porphyrin sensitizer (P type).

2. Materials and methods

2.1 Axially RPy-bonded tricationic P-porphyrins: (RPy3)2P(Tpp)3+

The preparation of tricationic bis[3-(1-alkyl-4-pyridinio)propoxo]tetraphenylporphyrinatophosphorus(V) complex, (RPy3)2P(Tpp)3+ (Tpp = tetraphenylporphyrinato group), was performed as follows [22]. Dichloro(tetraphenylporphyrinato)phosphorus chloride ([Cl2P(Tpp)]Cl [33], 300 mg) was reacted with 3-(4-pyridyl)-1-propanol (5.0 mL) in MeCN (30 mL) at reflux temperature for about 24 h until the Soret band shifted from 435 to 428 nm. Bis[3-(4-pyridyl)propoxo]tetraphenylporphyrinatophosphorus(V) chloride, (Py3)2P(Tpp)+, was produced in 47% yield. The (Py3)2P(Tpp)+ (50 mg) was reacted with alkyl halides (1.0 mL) in MeCN (25 mL) at reflux temperature for about 24 h to give (RPy3)2P(Tpp)3+ [22]. The yields of (RPy3)2P(Tpp)3+ are listed in Table 1.

SensitizersnbZaMetalYield /%ε/104 M−1 cm−1cCW/mM d
SoretQ
(MePy3)2P(tpp)1+3P9526.91.383.4
(BuPy3)2P(tpp)4+3P9323.11.186.1
(PentPy3)2P(tpp)5+3P3227.21.323.8
(HexPy3)2P(tpp)6+3P4731.31.455.8
(HeptPy3)2P(tpp)7+3P3226.71.266.0
(OctPy3)2P(tpp)8+3P4818.70.973.8
(HexPy3)2Sb(tpp)6+3Sb3516.34.1811.1
(MePy3)Sb(tpp)1+2Sb4212.74.452.4
(HexPy3)Sb(tpp)6+2Sb2515.14.485.2
(MePy5)2P(tpp)1+3P7328.21.36>120
(EtPy5)2P(tpp)2+3P5829.61.40>120
(ButPy5)2P(tpp)4+3P4425.31.29112
(HexPy5)2P(tpp)6+3P4424.71.2264
(4EtPy5)2P(tpp)2+3P7212.7 e0.57 e>120
(Me)2P(PyHex)6+2P5722.61.315.0
(Me1)2P(PyHex)6+2P7814.10.8911.4
(Bu1)2P(PyMe)1+2P9418.11.0113.6
(Bu2)2P(PyMe)1+2P3221.71.2113.0
(Hex2)2P(PyMe)1+2P4528.61.638.0

Table 1.

PDI of E. coli with cationic porphyrins.

Z = charge of the complex.


n = carbon number of the alkyl chain on the Ap.


Molar absorption coefficient for the Soret and the Q bands in MeOH solution.


CW = water solubility in mM.


Broadening of UV spectra occurred.


2.2 Axially RPy-bonded polycationic Sb-porphyrins

Axially RPy-bonded polycationic Sb-porphyrins were prepared using dibromo(tetraphenylporphyrinato)antimony bromide ([Br2Sb(Tpp)]Br) as the starting material [34]. The partial methanolysis of [Br2Sb(Tpp)]Br (1.077 g) was performed in MeOH-MeCN (1:1, 160 mL) in the presence of pyridine (0.75 mL) at 80°C until the Soret band shifted from 427 to 423 nm. Bromo(methoxo)-(tetraphenylporphyrinato)antimony bromide ([MeO(Br)Sb(Tpp)]Br, 520 mg) was formed in 61% yield [35]. An MeCN (20 mL) solution of [Br2Sb(Tpp)]Br (150 mg) and [MeO(Br)Sb(Tpp)]Br (180 mg) was heated with 3-(4-pyridyl)-1-propanol (3.7 mL) at refluxing temperature for about 24 h until the Soret band shifted to 418 nm, respectively. Thus, bis[3-(4-pyridyl)propoxo]tetraphenyl-porphyrinatoantimony (V) bromide ((Py3)2Sb(Tpp)+, 83 mg) and 3-(4-pyridyl)propoxo(methoxo)tetraphenylporphyrinatoantimony (V) bromide (Py3Sb(Tpp)+, 90 mg) were obtained in 50% and 43% yields, respectively. (Py3)2Sb(Tpp)+ (50 mg) was reacted with 1-bromohexane (0.5 mL) in MeCN (13 mL) at reflux temperature for about 24 h to give bis[3-(1-hexyl-4-pyridinio)-1-propoxo]-5,10,15,20-tetraphenylporphyrinatoantimony (V) tribromide ((HexPy3)2Sb(Tpp)3+, 20 mg, 35%). The reaction of (Py3Sb(Tpp)+, 50 mg) with MeI and 1-bromohexane (0.5 mL in MeCN (13 mL) at reflux temperature for about 24 h gave α-(methoxo)-β-[3(1-methyl-4-pyridinio)-1-propoxo]-5,10,15,20-tetraphenylporphyrinatoantimony (V) dibromide (MePy3Sb(Tpp)2+, 25 mg, 42%) and α-(methoxo)-β-[3 (1-hexyl-4-pyridinio)-1-propoxo]-5,10,15,20-tetraphenyl-porphyrinatoantimony (V) dibromide (HexPy3Sb(Tpp)2+, 20 mg, 25%), respectively [24].

2.3 Axially RPy-bonded tricationic P-porphyrins: (RPy5)2P(Tpp)3+

Bis[5-(3-alkyl-1-pyridinio)-3-oxapentyloxo]tetraphenylporphyrinato-phosphorus(V) dibromide, chloride ((RPy5)2P(Tpp)3+) was prepared from dihydroxo(tetraphenylporphyrinato)phosphorus chloride ([(HO)2P(Tpp)]Cl), which was prepared by hydrolysis of [Cl2P(Tpp)]Cl (300 mg) by refluxing in a mixed solvent of MeCN (160 mL) with pyridine (60 mL) and H2O (60 mL) [22]. Alkylation of [(HO)2P(Tpp)]Cl (80 mg) with di(2-bromoethyl) ether (1 mL) was performed in the presence of K2CO3 (19 mg) and 18-crown-6 ether (4.2 mg) in MeCN (5 mL) at 50°C to give bis(5-bromo-3-oxa-pentyloxo)tetraphenyl-porphyrinatophosphorus(V) chloride ((Br5)2P(Tpp)+). The (Br5)2P(Tpp)+ (50 mg) was reacted with 3-alkylpyridine (1.0 mL) in MeCN (10 mL) under heating at 100°C for 20–68 h for the preparations of (RPy5)2P(Tpp)3+ [22]. Similarly, bis[5-(4-ethyl-1-pyridinio)-3-oxapentyloxo]tetraphenylporphyrinatophosphorus(V) dibromide, chloride, (4EtPy5)2P(Tpp)3+ was prepared via the reaction of (Br5)2P(Tpp)+ (63 mg) with 4-ethylpyridine (1.0 mL) in dry MeCN (10 mL) at 100°C for 20 h.

2.4 RPy-bonded dicationic P-porphyrins at meso position: (R’m)2P(RPyTpp)2+

At first, 5,10,15-triphenyl-20-(4-pyridinyl)porphyrin (PyTpp) was prepared by reaction of pyrrole (1.55 mL), benzaldehyde (1.83 mL), and 4-formylpyridine (0.56 mL) in propanoic acid (100 mL) in an oil bath heated at 140°C for 1 h to give PyTpp (533 mg, 14%) [24]. PyTpp (101 mg) was reacted with phosphoryl chloride (POCl3, 2.0 mL) in pyridine (10 mL) in a pressure bottle heated at 180°C for 1 day to give dichloro[triphenyl(4-pyridinyl)porphyrinato]phosphorus chloride ([Cl2P(PyTpp)]Cl, 99.0 mg) in 81% yield. Substitution of the axial chloro ligand with a methoxo group was performed by refluxing [Cl2P(PyTpp)]Cl (82.7 mg) in MeOH (20 mL)-pyridine (0.25 mL) for 3 days until the Soret band shifted from 435 to 424 nm. Dimethoxo[5-(1-hexyl-4-pyridinio)-10,15,20-triphenyl-porphyrinato]phosphorus (V) dichloride ((Me)2P(HexPyTpp)2+) was prepared by reaction of [(MeO)2P(PyTpp)]Cl (62.0 mg) with 1-iodohexane (2 mL) in DMF (5 mL) in the presence of K2CO3 (19 mg) at 100°C for 2 h. (Me)2P(HexPyTpp)2+ was purified through anion exchange with chloride ions, as follows. An aqueous solution (10 mL) of AgBF4 (115 mg) was added to a MeCN-MeOH (1:1 v/v, 20 mL) solution of the porphyrins. After stirring for 24 h at room temperature, the solution was washed with water (100 mL) and an aqueous NaCl solution (100 mL) three times and subjected to precipitation with hexane (200 mL) [24].

[Cl2P(PyTpp)]Cl (78–100 mg) was reacted with ethylene glycol derivatives (H(OCH2CH2)mOR’, R’ = Me, n-Bu, n-Hex, 5–7 mL) in MeCN (10 mL) in the presence of pyridine (0.75 mL) for 24 h to give bis(2-alkyloxyethoxo)-5-(4-pyridinyl)-10,15,20-triphenylporphyrinatophosphorus (V) chloride ([(R’m)2P(PyTpp)]Cl) in 66–88%. Bis(2-methoxyethoxo)-5-(1-hexyl-4-pyridinyl)-10,15,20-triphenylporphyrinatophosphorus (V) bromide, chloride ((Me1)2P(HexPyTpp)2+) was prepared by reaction of [(Me1)2P(PyTpp)]Cl (51 mg) with 1-iodohexane (2 mL) in DMF (5 mL) in the presence of K2CO3 (19 mg) in an oil bath heated at 100°C for 2 h. After anion-exchange, dichloride salt of (Me1)2P(HexPyTpp)2+ (27 mg, 78%) was obtained. Also, other meso-RPy-bonded dicationic P-porphyrins (61–90 mg) were reacted with MeI (1.2 mL) in DMF (7.5 mL) in the presence of K2CO3 (43 mg) by heating at 100°C for 24 h to give an N-methyl-substituted complex. After anion exchange, (Me1)2P(HexPyTpp)2+ (35 mg, 94%), (Bu2)2P(MePyTpp)2+ (13.7 mg, 32%), and (Hex2)2P(MePyTpp)2+ (28.0 mg, 45%) were formed [24].

2.5 Preparation of E. coli suspension

E. coli K-12 (IFO 3301) was cultured aerobically at 30°C for 8 h in a LB medium (pH 6.5) consisting of bactotryptone (10 g L−1), yeast extract (5 g L−1), and NaCl (10 g L−1). After centrifugation of the cultured broth at 12,000 rpm for 10 min, the harvested cells were washed with physiological saline (NaCl, 7 g L−1) and then suspended in physiological saline, resulting in a cell suspension of E. coli. The cell concentrations were determined using a calibration curve and turbidity quantified by the absorbance measured at 600 nm on an UV–Vis spectrometer [24].

2.6 PDI of E. coli

PDI of E. coli was performed as follows. A phosphate buffer (0.1 M, pH 7.6) was prepared by dissolving Na2HPO4 (2.469 g) and NaH2PO4 (0.312 g) in 100 mL of water. The suspension of E. coli cells (1 × 105 cells mL−1, 1.0 mL), an aqueous solution of the studied sensitizers (25–100 μM, 0.1 mL), and the phosphate buffer (0.1 M, pH 7.6, 8.9 mL) were introduced into L-type glass tubes, resulting in a buffer solution (10 mL) containing E. coli (1 × 104 cells mL−1) and the studied sensitizers (0.25–1.0 μM). Under dark conditions, the L-type glass tubes were set on a reciprocal shaker and shaken at 160 rpm at room temperature for 2 h [24]. And then the L-type glass tubes were irradiated using a fluorescent lamp (Panasonic FL-15ECW, Japan; wave length = 400–723 nm; the maximum intensity: 545 nm; 10.5 W cm−2) on a reciprocal shaker at room temperature. A portion of the reaction mixture (0.1 mL) was taken up to 2 h at 20-min intervals and plated on LB plates. The LB plates were incubated for 30 h at 30°C.

The amount of the living cells (B) was defined as the average number of E. coli colonies that appeared after an incubation period of 30 h in three replicate plates. The B values for the PDI sensitizers were recorded at each irradiation time.

2.7 Fluorescence imaging

Incorporation of porphyrin sensitizers inside cells can be examined by fluorescence microscopy images of E. coli on a confocal laser scanning microscope (CLSM) under laser excitation at 543 nm. The aqueous solution containing the porphyrin sensitizers and E. coli was incubated for 3 h at 25°C. The concentrated solution was sandwiched between a cover slip and an agar pad on a bottom cover slip to maintain its position within the same focal plane [36].

3. Results

3.1 Properties of RPy-bonded P-porphyrins

Figure 2 shows the structures of the prepared porphyrins, which were water soluble due to cationic complexes. The water solubility (CW) is listed in Table 1. In addition, Table 1 lists the absorption coefficient (ε) of Soret band around 431 nm and Q-band at 562 nm in MeOH. These porphyrins could absorb strongly visible light. Moreover, they could generate 1O2 efficiently, since the quantum yields for the formation of 1O2 were found to be 0.88 for (HexPy3)2P(Tpp)3+ and 0.87 for (Bu2)2P(MePyTpp)2+ [23].

Figure 2.

Polycationic P- and Sb-porphyrins bonded to alkylpyridinium (RPy).

3.2 Results of PDI of E. coli

Results of PDI of E. coli are summarized in Table 2. As seen from Table 2, Meso-RPy-substituted P-porphyrins ((R’m)2P(RPyTpp)2+) have cytotoxicity, since E. coli was inactivated under dark conditions.

Sensitizers[P]/μM bAmount of bacteria ([B])/CFU mL−1a
t = 0/min c20406080100120
(MePy3)2P(tpp)2.0512 ± 22450 ± 14383 ± 13344 ± 20198 ± 13103 ± 4.527 ± 1.2
(BuPy3)2P(tpp)2.0377 ± 56216 ± 10105 ± 9.939 ± 5.318 ± 3.26.0 ± 2.72.3 ± 0.6
(PentPy3)2P(tpp)0.5105 ± 1265 ± 1236 ± 4.619 ± 3.814 ± 4.011 ± 3.17.0 ± 2.0
(HexPy3)2P(tpp)0.5243 ± 23156 ± 5.2125 ± 5.886 ± 3.177 ± 7.560 ± 1.217 ± 6.0
(HeptPy3)2P(tpp)0.4203 ± 16117 ± 9.153 ± 3.839 ± 3.115 ± 1.24.7 ± 2.13.0 ± 0
(OctPy3)2P(tpp)0.5294 ± 14215 ± 15194 ± 12136 ± 16103 ± 9.976 ± 1044 ± 8.0
(HexPy3)2Sb(tpp)1.0152 ± 7.1110 ± 4.776 ± 1749 ± 4.236 ± 1521 ± 4.545 ± 8.7
(MePy3)Sb(tpp)1.0170 ± 13167 ± 17134 ± 8.0126 ± 6.8102 ± 17108 ± 26113 ± 13
(HexPy3)Sb(tpp)1.0131 ± 28120 ± 1475 ± 1155 ± 1636 ± 1123 ± 3.513 ± 1.7
(MePy5)2P(tpp)1.029 ± 6.416 ± 4.212 ± 5.610 ± 1.013 ± 2.36.7 ± 2.16.7 ± 1.5
(EtPy5)2P(tpp)0.25167 ± 14141 ± 1859 ± 9.05.7 ± 0.61.7 ± 1.50.3 ± 0.60
(BuPy5)2P(tpp)0.25145 ± 11123 ± 7.692 ± 7.563 ± 4.633 ± 8.46.7 ± 4.94.7 ± 0.6
(HexPy5)2P(tpp)0.25213 ± 10213 ± 9.5176 ± 16166 ± 6.8140 ± 8.2132 ± 1297 ± 4.4
(4-EtPy5)2P(tpp)0.5139 ± 1485 ± 1388 ± 1662 ± 6.042 ± 8.732 ± 7.033 ± 1.5
(Me)2P(PyHex)2.090 ± 1388 ± 1749 ± 7.827 ± 6.217 ± 5.113 ± 1.515 ± 3.1
(Me1)2P(PyHex)0.589 ± 2.757 ± 2.942 ± 7.218 ± 3.516 ± 2.98.3 ± 4.05.7 ± 1.2
(Me1)2P(PyHex) d0.5109 ± 2699 ± 1359 ± 1264 ± 1065 ± 16559 ± 4241 ± 9.6
(Bu1)2P(PyMe)0.524 ± 3.620 ± 4.513 ± 3.012 ± 1.27.3 ± 2.93.7 ± 2.14.7 ± 1.2
(Bu1)2P(PyMe) d0.534 ± 5.025 ± 3.528 ± 6.131 ± 3.525 ± 1.520 ± 2.719 ± 2.1
(Bu2)2P(PyMe)2.0126 ± 1456 ± 3.821 ± 4.98.7 ± 2.13.3 ± 3.51.7 ± 0.62.3 ± 2.1
(Bu2)2P(PyMe) d2.0150 ± 13141 ± 5.5129 ± 8.3124 ± 11116 ± 1384 ± 1494 ± 12
(Hex2)2P(PyMe)1.063 ± 5.950 ± 7.556 ± 2.145 ± 8.139 ± 9.135 ± 6.133 ± 12

Table 2.

PDI of E. coli with cationic porphyrins under visible light irradiation.

PDI of E. coli was performed in a phosphate buffer solution (10 mL, pH 7.6) containing E. coli (ca. 2 × 104 cell mL−1) and porphyrin sensitizers under the irradiation of a fluorescent lamp. CFU = colony formation unit.


[P] was adjusted to attain the value of T1/2 between 20 and 120 min.


Irradiation time (t) in min.


Under dark conditions.


Based on Table 2, the survival ratios were calculated as 100B/B0 where B0 is the initial amount of bacteria. From the time-course plots of survival ratios (100B/B0), the half-life (T1/2 in min), i.e., the time required to reduce B from B0 to 0.5B0, was measured. A typical example of time-course plots is the case of PDI of E. coli by (HexPy3)2P(Tpp)3+ as shown in Figure 3. In this case, the T1/2 value of (HexPy3)2P(Tpp)3+ was determined to be 31 min. The minimum concentrations of the sensitizer [P] were adjusted such that T1/2 attained values between 20 and 120 min. Thus, the bactericidal activity (AF in μM−1 h−1) was evaluated using the following equation: AF = 60/([P] × T1/2). Table 3 summarizes [P] and AF values in the PDI of E. coli.

Figure 3.

Typical example of time-course plots of survival ratio (100B/B0) in the PDT of E. coli with (HexPy3)2P(Tpp)3+ (0.5 μM) under visible light irradiation (•) and under dark conditions (⃟). The T1/2 was determined to be 31 min from the plots.

SensitizeraZbMetalnc[P]/μM dT1/2 /min eAF /μM−1 h−1f
(MePy3)2P(tpp)+3P12.0660.5
(BuPy3)2P(tpp)+3P42.0271.1
(PentPy3)2P(tpp)+3P50.5294.1
(HexPy3)2P(tpp)+3P60.5313.8
(HeptPy3)2P(tpp)+3P70.4246.3
(OctPy3)2P(tpp)+3P80.5631.9
(HexPy3)2Sb(tpp)+3Sb61.0361.7
(MePy3)Sb(tpp)+2Sb11.01060.6
(HexPy3)Sb(tpp)+2Sb61.0680.9
(MePy5)2P(tpp)+3P11.0401.5
(EtPy5)2P(tpp)+3P20.25327.5
(ButPy5)2P(tpp)+3P40.25534.5
(HexPy5)2P(tpp)+3P60.251202.0
(4EtPy5)2P(tpp)+3P20.5502.4
(Me)2P(PyHex)+2P62.0450.7
(Me1)2P(PyHex)+2P60.5373.2
(Bu1)2P(PyMe)+2P10.5552.2
(Bu2)2P(PyMe)+2P12.0231.3
(Hex2)2P(PyMe)+2P11.01160.5

Table 3.

The [P], T1/2, and AF values in the PDI of E. coli by cationic porphyrins.

The PDI did not occur under dark conditions except for meso-RPy-substituted P-porphyrins, which were cytotoxic under dark conditions


Z = charge of the complex.


n = carbon number of the alkyl chain on the AP.


[P] = minimum concentrations of the porphyrins adjusted to attain the value of T1/2 between 20 and 120 min.


T1/2 = half-life in min.


AF = PDI activity in μM−1 h−1: AF = 60/([P] × T1/2).


3.3 PDI activity of the porphyrin sensitizers toward E. coli

As shown in Table 3, the AF values were dependent on the number of carbon atoms (n) in the alkyl group on the RPy group in (RPy3)2M(Tpp)3+ (M = P, Sb), RPy3Sb(Tpp)2+, and (RPy5)2P(Tpp)3+. Figure 4A shows the dependence of the AF values on n in the case of a series of (RPy3)2M(Tpp)3+ (M = P, Sb) and RPy3Sb(Tpp)2+. The maximum value of AF appeared at n = 7 whose [P] value was 0.40 μM. Moderately long alkyl chain made the sensitizer more active toward E. coli [24]. In the case of a series of (RPy5)2P(Tpp)3+ (Figure 4B), the maximum value of AF appeared at n = 2 whose [P] value for E. coli was 0.25 μM [25]. Therefore, the AF and [P] values of 3-ethyl analog were compared with those of 4-ethyl isomer. It was found that the AF value of 4-ethyl isomer was lower than that of 3-ethyl isomer. In the case of the 4-ethyl analog, broadening of Soret and Q bands occurred due to aggregation of porphyrin chromophores. It is suggested that aggregation caused to lower the AF value of 4-ethyl isomer (4EtPy5)2P(Tpp)3+).

Figure 4.

Relationship between the AF values and number of carbon atoms (n) in the alkyl group on the alkylpyridinium (RPy) in PDI of E. coli using (A) P-porphyrins ((RPy3)2P(Tpp)3+, ○) and Sb-porphyrins ((RPy3)2Sb(Tpp)3+ and RPy3Sb(Tpp)2+, ∆) and (B) 3-alkyl-substituted P-porphyrins ((RPy5)2P(Tpp)3+, ⃟) and their 4-ethyl-analog ((4EtPy5)2P(Tpp)3+, ◆).

Figure 5 shows the fluorescence images of E. coli in the presence of depicting the emission from (MePy3)2P(Tpp)3+ and (HexPy3)2P(Tpp)3+ inside E. coli. The images show that (HexPy3)2P(Tpp)3+ was accumulated inside E. coli, whereas (MePy3)2P(Tpp)3+ was not. (HexPy3)2P(Tpp)3+, which had a large affinity to E. coli, had the high PDI activity. The RPy group with a long alkyl chain made the sensitizer reactive toward E. coli.

Figure 5.

The incorporation of porphyrins inside bacteria through self-promoted mechanism. (i) Cationic porphyrin adsorbs to the anionic outer membrane; (ii) amphiphilic porphyrin interacts with hydrophobic parts of outer and inner membranes; (iii) porphyrin is incorporated inside the cell.

3.4 Comparison of the PDI activity in E. coli with the PDI activity in Saccharomyces cerevisiae

For comparison of the PDI activity in E. coli and other microorganisms, PDI of S. cerevisiae was performed using (RPy3)2P(Tpp)3+. It could photoinactivate S. cerevisiae in lower concentration compared with the case of E. coli [23]. For example, the [P] values of (MePy3)2P(Tpp)3+ for S. cerevisiae were 0.05 μM, while that for E. coli was 2.0 μM. Moreover, PDI of S. cerevisiae was performed using other porphyrins (Type E, Figure 6), which were monocationic and highly hydrophobic. The PDI of S. cerevisiae occurred efficiently by Type E porphyrins [37]. The [P] values for the PDI of S. cerevisiae were optimized to be 0.005 μM. Thus, S. cerevisiae has low drug resistance for hydrophobic sensitizers rather than polycationic sensitizers, since the [P] value of tricationic porphyrins was larger than that of monocationic porphyrins (Type E). On the contrary, no PDI of E. coli by Type E porphyrins occurred at all. This result shows that a more positive character is required for an efficient PDI of E. coli.

Figure 6.

Fluorescence images of E. coli obtained with a CLSM under laser-excitation at 543 nm. Fluorescence coming from inside the cells was observed with the addition of (HexPy3)2P(Tpp)3+ (D), but not observed with the addition of (MePy3)2P(Tpp)3+ (A). Transmission images of E. coli containing (HexPy3)2P(Tpp)3+ (E) and (MePy3)2P(Tpp)3+ (B). The image of C is obtained by overlapping images in A and B, and the image in F is obtained by overlapping images in D and E.

4. Discussion

The mechanism behind the PDI activity in E. coli is still not completely understood. However, it is known that the first contact of porphyrin photosensitizers occurs at the outer membrane. The outer leaflet of the outer membrane mainly consists of lipopolysaccharides and phospholipids, which are negatively charged and are stabilized with divalent cations such as Ca2+ and Mg2+ [38]. Therefore, electrostatic interaction between cationic photosensitizers and the outer leaflet instead of these divalent cations promotes destabilization of the outer membrane [39]. In the case of the cationic porphyrins with hydrophobic character, or the amphiphilic one, they can also interact with not only the outer leaflet but also the inner leaflet of the outer membrane and the plasma membrane (Figure 7). Thus, the amphiphilic porphyrins may be incorporated inside E. coli cells via the self-promoted uptake pathway [37]. The porphyrin sensitizers passed through the cell wall may reach biogenic proteins, lipids, and DNA. Under irradiation, reactive oxygen such as 1O2 was generated near to these molecules to induce cell death. Although E-type porphyrins generate 1O2 efficiently under visible light irradiation, the lifetime of 1O2 in aqueous medium is very short (~3 μs) [40]. Thus, for efficient PDI, 1O2 should be generated as close as possible to the target molecules. The P type porphyrins with amphiphilic characters, which can be incorporated inside E. coli, will be advantageous to PDI via 1O2 generation.

Figure 7.

P-porphyrins (Type E) substituted with alkylethyleneglycol ligands.

5. Conclusion

PDI of E. coli K-12 (IFO 3301) was examined using 19 kinds of cationic porphyrin sensitizers. In conclusion, (1) E. coli has high drug-resistance toward the hydrophobic and monocationic porphyrins such as Type E. (2) However, E. coli has low drug-resistance toward polycationic porphyrins such as Type P. (3) Especially, E. coli has low drug-resistance toward polycationic porphyrins with moderately long alkyl chain, for example, (HeptPy3)2P(Tpp)3+ and (EtPy5)2P(Tpp)3+. Alkyl chains might result in moderate hydrophobicity to take advantage of interaction between hydrophobic parts of cell membranes. (4) Polycationic porphyrins can interact with the anionic outer membrane at the first step and DNA and proteins inside the cells with strong binding affinities.

Acknowledgments

We thank Mr. Tomohiko Shinbara, Mr. Hiroki Kanemaru, Mr. Yusaku Suemoto, Mr. Kyosuke Takemori, Mr. Masato Shigehara, Mr. Kou Suzuki, Ms. Akari Miyamoto, and Hidekazu Uezono for their efforts on PDI of E. coli at University of Miyazaki.

Conflict of interest

The authors declare that they have no competing interests.

AFPDI activity (in μM−1 h−1): AF = 60/([P] × T1/2)
Bmount of bacteria
B0initial amount of bacteria
CFUcolony formation unit
CWwater solubility
εmolar absorption coefficient
LBLuria-Bertani medium
mnumber of ethylene glycol unit
ncarbon number of the alkyl chain on the Ap
[P]minimum effective concentrations of sensitizer
PDIphotodynamic inactivation
RPyN-alkylpyridinium group
tirradiation time
T1/2half-life time required to reduce B from B0 to 0.5B0
Zvalence number of the porphyrin complex
(Br5)2P(Tpp)+bis(5-bromo-3-oxapentyloxo)tetraphenylporphyrinato-phosphorus chloride
(Py3)2P(Tpp)+bis[3-(4-pyridyl)propoxo]tetraphenylporphyrinato-phosphorus chloride
(Py3)2Sb(Tpp)+bis[3-(4-pyridyl)propoxo]tetraphenylporphyrinato-antimony bromide
Py3Sb(Tpp)+3-(4-Pyridyl)propoxo(methoxo)tetraphenylporphyrinatoantimony bromide
PyTpptriphenyl(4-pyridinyl)porphyrin
(RPy3)2P(Tpp)3+bis[3-(1-alkyl-4-pyridinio)propoxo]tetraphenylpor-phyrinatophosphorus chloride, dihalide
(RPy3)2Sb(Tpp)3+bis[3-(1-alkyl-4-pyridinio)propoxo]tetraphenylpor-phyrinatoantimony tribromide
(RPy5)2P(Tpp)3+bis[5-(3-alkyl-1-pyridinio)-3-oxapentyloxo]tetraphenyl-porphyrinatophosphorus dibromide, chloride
RPy3Sb(Tpp)2+α-(methoxo)-β-[3-(1-hexyl-4-pyridinio)-1-propoxo]-5,10,15,20-tetraphenylporphyrinatoantimony (V) dibromide
(R’m)2P(RPyTpp)2+bis(2-alkyloxyethoxo)-5-(1-alkyl-4-pyridinio)-10,15,20-triphenylporphyrinatophosphorus (V) dichloride
TMPmeso-tetra[4-(1-methylpyridinium)]porphyrin

How to cite and reference

Link to this chapter Copy to clipboard

Cite this chapter Copy to clipboard

Jin Matsumoto, Tomoko Matsumoto, Kazuya Yasuda and Masahide Yasuda (December 28th 2018). Photodynamic Inactivation of <em>Escherichia coli</em> with Cationic Porphyrin Sensitizers, The Universe of Escherichia coli, Marjanca Starčič Erjavec, IntechOpen, DOI: 10.5772/intechopen.82645. Available from:

chapter statistics

233total chapter downloads

More statistics for editors and authors

Login to your personal dashboard for more detailed statistics on your publications.

Access personal reporting

Related Content

This Book

Next chapter

Introductory Chapter: The Versatile Escherichia coli

By Marjanca Starčič Erjavec

Related Book

First chapter

Lactic Acid Bacteria as Starter-Cultures for Cheese Processing: Past, Present and Future Developments

By J. Marcelino Kongo

We are IntechOpen, the world's leading publisher of Open Access books. Built by scientists, for scientists. Our readership spans scientists, professors, researchers, librarians, and students, as well as business professionals. We share our knowledge and peer-reveiwed research papers with libraries, scientific and engineering societies, and also work with corporate R&D departments and government entities.

More About Us