JPH0156077B2 - - Google Patents

Description

DETAILED DESCRIPTION OF THE INVENTION The present invention provides a novel antitumor substance SPF-100-F.
and its manufacturing method.

Conventionally, attenuated viable bacterial cells of hemolytic streptococcus have been prepared into preparations and have already been used as anticancer agents.

In addition, after crushing the bacterial cells of Streptococcus pyogenes, the active ingredients are extracted with water or a salt solution.
Add an organic solvent to precipitate the antitumor component,
A method for recovering hemolytic streptococci (Japanese Patent Publication No. 38-1647) and a method for lysing hemolytic streptococci with a lytic enzyme, lysozyme, cellulase, or proteolytic enzyme and fractionating the active fraction as a water-soluble fraction (British Patent No. 1163865) are known. It is being

As described above, it is widely known that Streptococcus bacteria themselves or their bacterial cell components have antitumor activity, but what was previously known was that the Streptococcus bacteria themselves or their cell components have antitumor activity. It was nothing more than matter. If you try to isolate the active ingredient from the bacterial body or inside the bacterial body,
It was necessary to fractionate the entire bacterial body by lysing it or mechanically crushing it. Such treatment complicates purification and makes it extremely difficult to isolate the active ingredient. Examples of proteins that have actually been separated and measured as active ingredients include a protein with a molecular weight of 200,000 (Japanese Patent Publication No. 48-43841, Japanese Patent Publication No. 44617-1972) and a glycoprotein with a molecular weight of 150,000 (Japanese Patent Publication No. 198-22026). That's about it.

The present inventors previously conducted research to find a method for eluting antitumor components into the culture filtrate of hemolytic streptococcus, and found that by adding penicillin or its related substances during culture, the antitumor components could be eluted. They discovered that SPF-1 was eluted into the culture solution (Japanese Patent Application Laid-Open No. 60-92218) and were able to isolate the physiologically active substance SPF-1 from the culture solution. (Japanese Patent Application Laid-Open No. 60-30689) As a result of intensive research in search of a better anti-tumor active ingredient for hemolytic streptococci, the present inventors fractionated a completely new anti-tumor substance SPF-100-F from culture. did.

The antitumor substance SPF-100-F of the present invention is excreted outside the bacterial cells during culture and becomes present in the culture solution, so it is sufficient to remove the bacterial cells by filtration and purify the culture filtrate. , isolation becomes much easier.

The antitumor substance SPF-100-F of the present invention is excreted into the culture medium and has a molecular weight of 9000 to 9000.
11000.

Until now, there have been no streptococcus-related antitumor substances that have accumulated in culture fluids, and no known molecular weight of less than tens of thousands of thousands of pounds.
SPF-100-FI is recognized as a completely new substance.

In addition, the antitumor substance SPF-100-F of the present invention
is recognized as a peptide substance based on elemental analysis, color reaction, etc., but it has a unique absorption in the ultraviolet absorption spectrum and is clearly different from conventionally widely known anti-tumor active substances. It is recognized as new.

The present invention relates to an antitumor substance SPF, which is characterized by culturing an antitumor substance SPF-100-F producing bacterium belonging to the genus Streptococcus and collecting the antitumor substance SPF-100-F from the culture. -100-F
This includes the manufacturing method of

In the present invention, bacteria that produce the antitumor substance SPF-100-F belonging to the genus Streptococcus are widely used, one example of which is Streptococcus pyogenes.
ATCC 21060, Streptococcus sp. ATCC 21597, Streptococcus pyogenes
ATCC 21546, Streptococcus pyogenes
ATCC 21547 and Streptococcus pyogenes ATCC 21548.

The culture medium is meat extract medium, mother extract medium, brain heart infusion medium (BHI
Natural media such as Streptococcus spp.) are often used, but general media containing carbon sources, nitrogen sources, etc. can also be used as long as they allow Streptococcus bacteria to grow effectively.

Culture at PH5.0-8.0, preferably 6.1-7.2 and 30-30
It is common to perform static culture at 40° C., preferably 35 to 37° C., in an anaerobic manner, but other modified methods such as stirring culture may also be employed.

In the present invention, adding penicillin or its related substances at an appropriate time during culture plays an important role in obtaining the antitumor substance SPF-100-F.

The timing of addition of penicillin or related substances is 37℃.
The period of time is preferably 3 to 20 hours, particularly 5 to 10 hours after the culture reaches logarithmic growth phase. Thereafter, by continuing the culture for 1 hour to 20 hours, preferably 3 to 15 hours, antitumor substances are added to the culture solution.
A large amount of SPF-100-F can be accumulated.

Penicillin or its related substances may be any known related substances that have similar effects to penicillin, but penicillin G is commonly used. The amount added is 100~ for penicillin G.
About 3000 units/ml, preferably 300 to 1500 units/ml of culture solution is sufficient.

The resulting culture solution is centrifuged to remove bacterial cells, ammonium sulfate is added to the filtrate, a fraction with a saturation level of 50 to 90% is collected, and the resulting precipitate is dissolved in a buffer solution.

A solution containing the antitumor substance SPF-100-F can be stored in a frozen state or by lyophilization. This material can be further purified by contacting it with an ion exchanger or gel filtration agent, if necessary. Ion exchange resins, ion exchange cellulose, ion exchange Cephadex (manufactured by Pharmacia), hydroxyapatite, etc. are used as ion exchangers, and as gel filtration agents, Toyo Pearl
HW50F (manufactured by Toyo Soda Co., Ltd.), Cephadex (manufactured by Pharmacia), etc. are used. In the main purification process, purification is carried out by a batch method using the above-mentioned carrier, or by a flow method after filling a column with the carrier. The antitumor substance SPF-100-FI can be obtained by subjecting the specimen obtained by the above purification method to high performance liquid chromatography using a G3000SW column (manufactured by Toyo Soda Co., Ltd.).

Antitumor substance SPF of the present invention obtained in Example 1
-100-FI is a peptide substance that becomes a pale yellow powder when freeze-dried.

Next, we will show the physicochemical properties of the antitumor substance SPF-100-F.

1 Elemental analysis C 45.22-45.46 H 6.15-6.22 N 11.23-11.48 O 36.26-34.48 Ash 1.14-2.36 2 Molecular weight When measured by gel filtration method, the molecular weight is 9000~
It is 11000.

3 Decomposition point This substance turns brown at 160℃ and turns black at 200℃ and decomposes.

4 Specific rotation [α] ²⁰ _D = -80 to -84 (C = 1.00) 5 Ultraviolet absorption spectrum The ultraviolet absorption spectrum of a 0.1% aqueous solution of this substance is shown in FIG. It has absorption at 320nm and 280nm, which is characteristic.

6 Infrared absorption spectrum It is shown in FIG.

3300cm ^-1 , 2970cm ^-1 , 1640cm ^-1 , 1530cm
^-1 , 1450cm ^-1 , 1400cm ^-1 , 1320cm ^-1 , 1260cm
Absorption is observed at ^-1 , 1090cm ^-1 and 540cm ^-1 .

7 Solubility in solvents Soluble in water, but poorly soluble or Insoluble.

8 Distinction between basic, acidic, and neutral The pH of a 0.1% aqueous solution of this substance is 6.95.

9 Color of matter It is a pale yellow powder.

10 Color reaction Ninhydrin reaction + Beurets reaction + Moritshu reaction ± orsine hydrochloric acid reaction − Anthrone reaction + cysteine sulfuric acid reaction ± Each coloring reaction of Moritzhu reaction, orsine hydrochloric acid reaction, Anthrone reaction, and cysteine sulfuric acid reaction was performed using a 0.1% aqueous solution. I went.

11 Stabilization This substance is stabilized by the addition of L-cysteine, dithiothreitol (DDT), glycerol, albumin, globulin, α- and β-cyclodextrin, (NH ₄ ) ₂ SO ₄ , salt, etc. .

Next, examples of the present invention will be shown.

In addition, the antitumor substance SPF-100- in Examples
The activity unit of F was measured using the Udaka method (Journal of
Antibiotics vol 35(10), 1312-1318 (1982);
Journal of Antibiotics vol 35No.10 1319―1325
OCT 1982). For the measurement, a polymer-permeable E. coli mutant strain UR-3 is used, and a bioassay is performed using antibacterial activity against UR-3 as an indicator.

That is, a medium (M3 medium) consisting of 1.75% Bacto Antibiotic Medium 3 (manufactured by Difco) and 1.3% agar ( _M3 medium) was heat sterilized at 120°C for 15 minutes.
Dispense ml into a petri dish and let it cool to prepare a plate medium.

Meanwhile, peptone 0.5%, meat extract 0.5%,
A medium consisting of 0.3% NaCl and 0.8% agar was heated at 120℃ for 15 minutes.
Sterilize by heating for a minute. After that, keep it in a constant temperature bath at 42°C, and when the temperature of the medium reaches 42°C, add UR-3 bacteria, which had been previously cultured at 37°C for 17 hours, to the medium so that 10 ⁴ cells are present in 1 ml. by pipette 2
Collect ml and add it to the surface of _M3 medium prepared in advance and spread quickly and uniformly to solidify. Appropriately dilute the test solution containing the antitumor substance SPF-100-F, and pour 0.05 ml of the solution onto paper.
Let it soak into a disk (diameter 8 mm) (Toyo Roshi). This paper disk was placed on the plate prepared above, incubated at 37°C for 17 hours, and treated with the antitumor substance.
Measure the size of the inhibition circle created by SPF-100-F. The concentration of the antitumor substance SPF-100-F that gives an inhibition circle diameter of 10 mm is defined as 1 unit (1U).

Method for measuring antitumor activity Antitumor activity was measured by measuring the growth inhibition rate (IR%) of cultured cells L1210. L 1210
Cells were grown in RPMI 1640 medium (5mg/10% FBS).
(containing kanamycin). This culture solution
0.5 ml was poured into a Falcon 2058 tube so that the number of cells was 1×10 ⁵ cells/tube. Next, add a predetermined amount of the standard (anti-tumor substance SPF) to this culture solution.
-100-F) dissolved in the culture solution to the desired concentration was added to the culture medium, and the cells were cultured at 37°C in the presence of 5% _CO2 . 48 hours after adding the standard, staining with trypan blue was performed, and IR was determined using the following formula.
(%) was calculated.

IR (%) = (A) - Number of viable cells in each experimental group/Number of viable cells in control group x 100 Here, (A) indicates the number of viable cells in the control group.

A control was performed at the same time using 0.5 ml of culture solution that did not contain the standard.

Example 1 Table 1 Medium A Maltose 0.25% Meat extract 1.0% Polypeptone 1.0% Yeast extract 0.25% Potassium phosphate 0.1% Magnesium sulfate 0.05% Sodium chloride 0.1% PH6.7 Streptococcus pyogenes ATCC 21060 BHI
100 ml of the seed culture was inoculated into 100 ml of the medium and statically cultured at 37°C for 8 hours, then inoculated into medium A1 and precultured under the same conditions as the seed culture.

This pre-culture solution was inoculated into medium A8, and cultured at 37°C for 14.5 hours using a 10 jar fermenter.
After culturing anaerobically at 300 rpm, penicillin G is added to 1000 units/ml and the culture is continued for an additional 5 hours.
The obtained culture solution is centrifuged to remove bacterial cells.

Ammonium sulfate is added to the culture solution, and a fraction with a saturation level of 50 to 90% is collected to obtain a precipitate containing the antitumor substance SPF-100-F. The entire amount of this precipitate is dissolved in 300 ml of a buffer containing a stabilizer, and added to a DEAE-cellulose column (5.0 x 70 cm) for adsorption. to this
The active portion of UR-3 is fractionated by stepwise elution with a buffer containing 0.3M sodium chloride.

Furthermore, this eluate is concentrated, adsorbed onto a gel filtration agent Toyopearl HW 50F column (12.6 x 100 cm), eluted with a buffer solution, and the active portion of UR-3 is fractionated and concentrated. This concentrated solution was subjected to high performance liquid chromatography using a TSK-GEL G 3000SW (Toyo Soda Kogyo Co., Ltd. 0.75 x 60 cm) column. This elution curve is shown in FIG.

Here, the A fraction was designated as SPF-100-F, and the B fraction was designated as SPF-100-F. Fraction A was lyophilized. This freeze-dried product contains anti-tumor substance SPF.
-100-F, and 43 mg was obtained. SPF-100-F
The antitumor activity of this drug as a test drug was confirmed in an in vitro experiment as shown in Experimental Example 1.

Example 2 Streptococcus pyogenes ATCC
Example 1 using 21060 in medium A shown in Table 1.
It was cultured in the same way. In this case, penicillin G
The mixture was added at a concentration of 300 units/ml culture solution, and the culture was continued for an additional 10 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain antitumor component SPF-100-F.
Obtained 18 mg.

Example 3 Streptococcus pyogenes ATCC 21060
were cultured in the same manner as in Example 1 using medium A shown in Table 1. In this case, penicillin G was added at a concentration of 3000 units/ml culture solution, and the culture was further incubated for 3
Lasted for an hour. This culture filtrate was purified in the same manner as in Example 1 to obtain 61 mg of the antitumor component SPF-100-F.

Example 4 Streptococcus pyogenes ATCC 21060
were cultured in the same manner as in Example 1 using medium B shown in Table 2. In this case, penicillin G is 1000 units/
ml culture solution, and culture was continued for an additional 5 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain 32 mg of the antitumor component SPF-100-F.

Table 2 Medium B Maltose 0.1% Meat extract 0.5% Polypeptone 1.0% Yeast extract 0.25% Sodium chloride 0.1% PH=7.2 Example 5 Streptococcus pyogenes ATCC 21060
in the same manner as in Example 1 using medium C shown in Table 3.
Cultured at 35°C. In this case, penicillin G is 1000
The solution was added at a concentration of 1 unit/ml culture solution, and the culture was continued for an additional 5 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain 14 mg of the antitumor component SPF-100-F.
I got it.

Table 3 Medium C Maltose 0.1% Meat extract 0.5% Polypeptone 0.5% Casamino acids 0.3% Yeast extract 0.5% Acidic potassium monophosphate 0.1% Magnesium sulfate 0.05% PH=6.5 Example 6 Streptococcus pyogenes ATCC 21060
were cultured in the same manner as in Example 1 using medium D shown in Table 4. In this case, penicillin G is 1000 units/
ml culture solution, and culture was continued for an additional 5 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain 49 mg of the antitumor component SPF-100-F.

Table 4 Culture D Maltose 0.25% Casamino acids 0.3% Yeast extract 1.0% Acidic monobasic potassium phosphate 0.1% Magnesium sulfate 0.05% PH=6.9 Example 7 Streptococcus sp. ATCC 21597 was grown in medium A shown in Table 1. The cells were cultured in the same manner as in Example 1. In this case, penicillin G is 1000 units/
ml culture solution, and culture was continued for an additional 5 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain 39 mg of the antitumor substance SPF-100-F.

Example 8 Streptococcus pyogenes ATCC 21546
were cultured in the same manner as in Example 1 using medium A shown in Table 1. In this case, penicillin G is added at 1000 units/ml culture solution, and the culture is further
Lasted for an hour. This culture filtrate was purified in the same manner as in Example 1 to obtain 51 mg of the antitumor component SPF-100-F.

Example 9 Streptococcus pyogenes ATCC 21547
were cultured in the same manner as in Example 1 using medium A shown in Table 1. In this case, penicillin G is added at 1000 units/ml culture solution, and the culture is further
Lasted for an hour. This culture filtrate was purified in the same manner as in Example 1 to obtain 38 mg of the antitumor component SPF-100-F.

Example 10 Streptococcus pyogenes ATCC 21548
were cultured in the same manner as in Example 1 using medium A shown in Table 1. In this case, penicillin G is added at 1000 units/ml culture solution, and the culture is further
Lasted for an hour. This culture filtrate was purified in the same manner as in Example 1 to obtain 47 mg of the antitumor component SPF-100-F.

Example 11 Streptococcus pyogenes ATCC 21060
were cultured in the same manner as in Example 1 using medium A shown in Table 1. In this case, cephalosporin C is
The mixture was added at a concentration of 6000 μg/ml culture solution, and the culture was continued for an additional 5 hours. This culture filtrate was purified in the same manner as in Example 1 to obtain antitumor component SPF-100-F.
13 mg was obtained.

Experimental Example 1 Antitumor component SPF-100 obtained in Example 1
The in vitro antitumor activity test of F was conducted using the method for measuring antitumor activity described in the text, and the results are shown in Table 5.

Table-5 Results of antitumor activity of SPF-100-F SPF-100-F (mg/ml) IR% 0.125 100.0 0.05 45.2 0.025 36.6 0.013 24.2

[Brief explanation of drawings]

Figure 1 shows the ultraviolet absorption spectrum of the antitumor substance SPF-100-F, and Figure 2 also shows the infrared absorption spectrum. FIG. 3 is a diagram showing the elution curve of the active fraction in Example 1 in high performance liquid chromatography using a TSK-GEL G 3000 SW column.

Claims (1)

[Claims] 1. An antitumor substance having the following physicochemical properties:
SPF-100-FI. 1 Elemental analysis C 45.22-45.46% H 6.15-6.22% N 11.23-11.48% O 36.26-34.48% Ash 1.14-2.36% 2 Molecular weight When measured by gel filtration method, the molecular weight is approximately 9000-
It is 11000. 3. Decomposition point This substance turns brown at 160℃ and turns black at 200℃ and decomposes. 4 Specific rotation [α] ²⁰ _D = -80° to -84° (C = 1.00) 5 Ultraviolet absorption spectrum In the ultraviolet absorption spectrum of a 0.1% aqueous solution of this substance, absorption is observed at 320 nm and 280 nm. 6 Infrared absorption spectrum Absorption is observed at 3300cm ^-1 , 2970cm ^-1 , 1640cm ^-1 , 1530cm ^-1 , 1450cm ^-1 , 1400cm ^-1 , 1320cm ^-1 , 1260cm ^-1 , 1090cm ^-1 and 540cm ^-1 . 7 Solubility in solvents Soluble in water, but poorly soluble or Insoluble. 8. Distinction between basic, acidic, and neutral The pH of a 0.1% aqueous solution of this substance is 6.95. 9. Color of substance: Pale yellow powder. 10 Color reaction Ninhydrin reaction + Beurets reaction + Mauritsch reaction ± orsine hydrochloric acid reaction − Anthrone reaction + cysteine sulfate reaction ± 11 Stabilization This substance contains L-cysteine, dithiothreitol (DTT), glycerol, albumin, globulin, α- and It is stabilized by the addition of β-cyclodextrin (NH ₄ ) ₂ SO ₄ , salt, etc. 2 Antitumor substance belonging to the genus Streptococcus
A method for producing an antitumor substance SPF-100-F, which comprises culturing SPF-100-F producing bacteria and collecting the antitumor substance SPF-100-F from the culture. 3 Antitumor substance belonging to the Streptococcus genus
SPF, an antitumor substance according to claim 2, characterized in that when culturing the SPF-100-F producing bacteria, penicillin or a related substance is added at an appropriate time during the culture. -100-F
manufacturing method.