CN110922382A

CN110922382A - iso-Penicillium xanthone A from penicillium oxalicum and application in lymphoma

Info

Publication number: CN110922382A
Application number: CN201811474254.1A
Authority: CN
Inventors: 陈立; 李钰莹; 李欣欣; 王思远; 刘沁颖; 程苗苗; 张其清
Original assignee: Fuzhou University
Current assignee: Fuzhou University
Priority date: 2018-12-04
Filing date: 2018-12-04
Publication date: 2020-03-27

Abstract

The invention relates to iso-Penicillium xanthone A derived from Penicillium oxalicum and its application in lymphoma. The compound is characterized by comprising the following structural characteristics:

Description

iso-Penicillium xanthone A from penicillium oxalicum and application in lymphoma

Technical Field

The invention relates to iso-Penicillium xanthone A derived from penicillium oxalicum and application thereof in lymphoma, belonging to the field of biological medicine.

Background

With the development of science and technology, the medical level of our medicine has been improved, but the incidence of cancer is on the rise, which is the second leading cause of death worldwide. Malignant Lymphoma (ML) is a general term for a group of malignant tumors originating from lymphohematopoietic system, and is a blood system with the fastest increasing incidence rate, the early symptoms of which are atypical, the individual differences of the first symptoms of which are large, and the lesions can occur anywhere in the body, which is called "chameleon" in the tumor. Malignant lymphoma often occurs in young and strong years, and the cause of the disease is unknown so far.

Penicillium anthrone is an anthraquinone organic compound produced by secondary metabolism of fungi, and is first obtained from Penicillium anthrone A in 2002Penicillium thomiiTo date, over a decade has passed. The compounds are reported to date as 2, each of which is penam A, B and all of which are 2-4' linked. The compound has obvious inhibition on tumor cells, and is an ideal raw material for developing antitumor drugs or tumor cell proliferation inhibitors. But the research on the antitumor activity of their enantiomers is still blank.

The present inventors have studied and found that Penicillium oxalicum (Penicillium oxalicum) IBPT-6, (deposited at the chinese type culture collection on 25.12.2013, address: wuhan, Wuhan university, the accession number is: CCTCC NO: m2013714), and the active ingredients thereof were studied. Researches show that the penicillium anthrone compound has anti-human lymphoma activity, and no report of the proliferation inhibition activity of the compound on human lymphoma cells exists at present, so that no related medicine exists in the market.

Disclosure of Invention

The invention aims to provide iso-Penicillium xanthone A derived from penicillium oxalicum and application thereof in lymphoma. The compound has effects of inhibiting lymphoma cell proliferation, and resisting human lymphoma. The structural formula is as follows:

。

the preparation method of the compound is to culture penicillium oxalicum (A)Penicillium oxalicum) IBPT-6, obtaining fermented mycelium, and separating and purifying the compound from the mycelium. The method comprises the following specific steps:

1 fermentation production

Culturing microorganism by conventional method, collecting Penicillium oxalicum (B) ((B))Penicillium oxalicum) IBPT-6 is inoculated on a flat solid culture medium, cultured in an incubator at 28 ℃ for 2-3d, then inoculated in a fungus culture medium, statically cultured at 28 ℃ for 30 d, and filtered by a plurality of layers of gauze to obtain mycelium and fermentation liquor; the fungus culture medium comprises the following components: 10.0 g of glucose, 20.0g of maltose, 20.0g of mannitol, 10.0 g of monosodium glutamate, 3.0 g of yeast extract, 15.0 g of NaCl and KH₂PO₄0.5 g、MgSO₄·7H₂O0.3 g and ultrapure water were added to the reaction solution to a constant volume of 1L.

2 obtaining of extract

The mycelium and the fermentation broth were separated with gauze. Continuously performing ultrasonic wall breaking on the mycelia for 3 times by using an acetone solution (containing 20-30% of water), and filtering to remove residues to obtain a crude extract of the mycelia containing acetone and water. Concentrating under reduced pressure to remove acetone to obtain water solution of crude extract, extracting with ethyl acetate at volume ratio of the water solution to ethyl acetate of 1:2 for 3 times to obtain ethyl acetate crude extractive solution, concentrating, and evaporating to obtain mycelium extract 36.5 g.

3 separation and purification of Compound

The mycelium extract is mixed with 100-plus 200-mesh silica gel, and the mixture is mixed with petroleum ether: dichloromethane: methanol is used as gradient eluent, and decompression silica gel chromatographic column chromatography is carried out. The components A-E are separated by simple thin-layer chromatography analysis, combination and separation. Component C (12)7 g) with dichloromethane: methanol =1:2 as gradient eluent, performing gel column chromatography (Sephadex LH-20), and mixing to obtain four subfractions C after thin layer chromatography₁-C₄. Subfraction C₃(4.9 g) by semi-preparative liquid chromatography (type 1010 ODS-A, 10X 250 mm, 5 μm): the isolation flow was 5 mL/min and the mobile phase was 55% acetonitrile with 0.1% TFA to give the indicated compound (510mg, t)_R22.8 min)。

Said penicillium oxalicum (A), (B)Penicillium oxalicum) IBPT-6, which has been deposited at the China center for type culture Collection on 25.12.2013, address: wuhan, Wuhan university, the accession number is: CCTCC NO: m2013714.

The invention also comprises the application of the compound in preparing medicaments for inhibiting human lymphoma cell proliferation and the application of the compound in preparing medicaments for resisting human lymphoma.

The invention has the following remarkable advantages: researches show that the penicillium anthrone compound has remarkable activity of inhibiting human lymphoma cell proliferation, and no report of the compound on the activity of inhibiting human lymphoma cell proliferation exists at present, so that no medicine related to the activity is found in the market.

Drawings

FIG. 1 major COSY, HMBC and NOE signals of Iso-Penicillixanthone A.

Detailed Description

The chemical structures of the compounds referred to in the examples below:

EXAMPLE 1 fermentative production and isolation purification of the Compound

1 fermentation production

Fermentation culture of producing bacteria: taking Penicillium oxalicum (B) according to a conventional method for culturing microorganismsPenicillium oxalicum) IBPT-6 (deposited in the China center for type culture Collection on 25.12.2013, address: wuhan, Wuhan university, the accession number is: CCTCC NO: m2013714) in proper amount, inoculating on a flat solid culture mediumCulturing at 28 deg.C for 2-3 d.

Taking flat plate to culture 2-3d penicillium oxalicum (Penicillium oxalicum) An appropriate amount of IBPT-6 was inoculated into a container containing 400 mL of culture broth [ composition of culture broth (g/L): 10.0 parts of glucose, 20.0 parts of maltose, 20.0 parts of mannitol, 10.0 parts of monosodium glutamate, 3.0 parts of yeast extract, 15.0 parts of NaCl and KH₂PO₄0.5、MgSO₄·7H₂O0.3, and the volume of ultrapure water is up to 1L]And performing static culture at 28 ℃ for 30 days to obtain mycelium and fermentation liquor.

2 obtaining of extract

The mycelium and the fermentation broth were separated with gauze. Continuously performing ultrasonic wall breaking on the mycelia for 3 times by using an acetone solution (containing 20-30% of water), and filtering to remove residues to obtain a crude extract of the mycelia containing acetone and water. Concentrating under reduced pressure to remove acetone to obtain water solution of crude extract, extracting with ethyl acetate at volume ratio of 1:2 for 3 times to obtain ethyl acetate crude extractive solution, and concentrating under reduced pressure to near dry to obtain mycelium extract 36.5 g.

3 separation and purification of Compound

The mycelium extract is mixed with 100-plus 200-mesh silica gel, and the mixture is mixed with petroleum ether: dichloromethane: methanol is used as gradient eluent, and decompression silica gel chromatographic column chromatography is carried out. By simple thin layer chromatography, combining, and separating into components A-E. Component C (12.7 g) was purified in dichloromethane: methanol =1:2 as gradient eluent, performing gel column chromatography (Sephadex LH-20), and mixing to obtain four subfractions C after thin layer chromatography₁-C₄. Subfraction C₃(4.9 g) by semi-preparative liquid chromatography (type 1010 ODS-A, 10X 250 mm, 5 μm): the isolation flow was 5 mL/min and the mobile phase was 55% acetonitrile with 0.1% TFA to give the indicated compound (510mg, t)_R22.8 min)。

Compound (I) is yellow powder at room temperature, [ α ]]²⁰ _D+ 105.6° (c 1, pyridine); [α]²⁰ _D+ 3.1°(c 1, Me₂CO) high resolution electrospray mass spectrometry HRESI-MS at m/z: 661.1550 shows molecular ion peak [ M + Na]⁺（calcd for C₃₂H₃₀NaO₁₄661.1533); molecular weight at 638, estimated from spectral informationSub-formula is C₃₂H₃₀O₁₄。¹H and¹³the C-NMR data are shown in Table 1, and the main COSY, HMBC and NOE signals are shown in FIG. 1.

Of the compounds of Table 1¹H and¹³C-NMR data (500 MHz)¹H and 126 MHz¹³C, in DMSO-d ₆）

Example 2 in vitro testing of antitumor Activity

1 Experimental sample and experimental method

Preparing a solution of a sample to be detected: the test sample was the purified compound isolated and purified in example 1. Precisely weighing a proper amount of sample, preparing a 100 mM mother solution by DMSO, filtering and sterilizing by a filter membrane, and storing at-20 ℃ for later use. The proportion of DMSO is controlled below 1 per mill.

Taking out frozen cell strain from liquid nitrogen, rapidly melting in 37 deg.C water bath, centrifuging at 1200 rpm for 5 min, discarding frozen solution, adding 1 mL culture medium, pumping into culture flask, adding 5 mL fresh DMEM or RPMI 1640 culture medium, gently shaking to uniformly suspend cells in culture medium, standing at 37 deg.C and 5% CO₂Cultured in an incubator. When the cell density reaches about 90%, passage is carried out, old culture medium is removed, PBS is washed for 2 times, 300 mu L of pancreatin is added (the pancreatin can cover the bottom of the bottle), the cell is digested in an incubator at 37 ℃ until the cell becomes round and is about to fall off, the culture medium containing 10% fetal calf serum is added to stop the digestion, the cell is divided into 2-3 new culture bottles after being blown and evenly mixed, and the culture medium is supplemented to ensure that the cell continues to grow in the incubator.

Cell proliferation inhibitory Activity test method (WST-1 method)

The activity evaluation of the anti-tumor cells adopts a WST-1 kit detection method, and the cell concentration is adjusted to be 3 multiplied by 10 after the tumor cells in the logarithmic growth phase are digested⁴a/mL single cell suspension, 100 μ L of the cell suspension was mixed and inoculated into a 96-well plate, 5 replicate wells per concentration. Then placing at 37 ℃ and 5% CO₂The culture was carried out overnight in an incubator. Removing supernatantSolution, drug diluted to different concentrations with medium was added to the corresponding 96-well plate, and control group was added with medium containing the same amount of DMSO. After culturing for 72 h, adding 10 mu L of WST-1 solution into each well, incubating for 2 h at 37 ℃, gently shaking and uniformly mixing, and measuring the light absorption value at 450 nm by using a microplate reader. The mean OD value for 5 wells was calculated and calculated according to the formula: cell proliferation inhibition rate = (OD control group-OD blank group)/(OD experimental group-OD blank group) × 100% the proliferation inhibition rate of each concentration of drug on tumor cells was calculated, and half inhibition rate IC was calculated using Graphpad prism5.0 software₅₀。

2 results of the experiment

The results of the cell proliferation inhibitory activity test are shown in Table 2.

TABLE 2 inhibitory Activity of Compounds on human lymphoma cell proliferation

3 conclusion

The compound has good anti-tumor activity on human lymphoma cells. Can be used for preparing lymphoma cell proliferation inhibiting medicine or antitumor medicine for lymphoma research.

Claims

1. Compound (I)

Characterized in that the compound is prepared by the following method: fermented Penicillium oxalicum (Penicillium oxalicum) IBPT-6, obtaining a fermentation product, and then separating and purifying the fermentation product to obtain the compound; wherein said Penicillium oxalicum (A), (B)Penicillium oxalicum) IBPT-6, which has been deposited at the China center for type culture Collection on 25.12.2013, address: wuhan, Wuhan university, the accession number is: CCTCC NO: and M2013714.

2. Use of a compound according to claim 1 for the preparation of a medicament for inhibiting the proliferation of lymphoma cells.

3. Use of a compound according to claim 1 for the preparation of an anti-lymphoma medicament.