EP4267721A1 - Souches bactériennes pour la production de biocellulose - Google Patents
Souches bactériennes pour la production de biocelluloseInfo
- Publication number
- EP4267721A1 EP4267721A1 EP21840612.2A EP21840612A EP4267721A1 EP 4267721 A1 EP4267721 A1 EP 4267721A1 EP 21840612 A EP21840612 A EP 21840612A EP 4267721 A1 EP4267721 A1 EP 4267721A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- biocellulose
- rscic
- dps
- efl
- access
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N1/00—Microorganisms; Compositions thereof; Processes of propagating, maintaining or preserving microorganisms or compositions thereof; Processes of preparing or isolating a composition containing a microorganism; Culture media therefor
- C12N1/20—Bacteria; Culture media therefor
- C12N1/205—Bacterial isolates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/10—Transferases (2.)
- C12N9/1048—Glycosyltransferases (2.4)
- C12N9/1051—Hexosyltransferases (2.4.1)
- C12N9/1059—Cellulose synthases (2.4.1.12; 2.4.1.29)
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12P—FERMENTATION OR ENZYME-USING PROCESSES TO SYNTHESISE A DESIRED CHEMICAL COMPOUND OR COMPOSITION OR TO SEPARATE OPTICAL ISOMERS FROM A RACEMIC MIXTURE
- C12P19/00—Preparation of compounds containing saccharide radicals
- C12P19/04—Polysaccharides, i.e. compounds containing more than five saccharide radicals attached to each other by glycosidic bonds
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12R—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES C12C - C12Q, RELATING TO MICROORGANISMS
- C12R2001/00—Microorganisms ; Processes using microorganisms
- C12R2001/01—Bacteria or Actinomycetales ; using bacteria or Actinomycetales
- C12R2001/07—Bacillus
Definitions
- the present application relates to the field of microbiology and in particular isolated and verified bacterial strains for biocellulose production .
- a bacterial cultivation system for the production of cellulose gel (HSBC) containing Gluconacetobacter xylinus (G. xylinus) in an interface system between an aqueous and an oily phase in the presence of glucose and mannitol at 30°C is known (Horu Hoshia, Kazuyoshi Yamazakia, Yuki Satob, Takaya Shidaa, Takao Aoyagia, Production of hollow-type spherical bacterial cellulose as a controlled release device by newly designed floating cultivation, Heliyon 4, 2018, e00873) .
- the inventors of the present invention have isolated new bacterial strains belonging to the genus Bacillus and Brevundimonas capable of producing biocellulose.
- Said strains have peculiar characteristics compared to strains known in the art. In particular, they are able to synthesise biocellulose under room temperature conditions, i.e. without energy expenditure, compared to known processes which take place at a temperature of around 30°C. In the process, no specific saline solutions are used or prepared, but plain water is used, and the culture medium is not a limiting factor and different types can be used in the bacterial culture without affecting the success of the process for biocellulose production. In contrast to what is known in the art in which the culture media are added with glucose and mannitol, the former at concentrations of at least 3%, in the culture of the present invention glucose or fructose at 1.5% is added.
- Another object of the present ibnvention is the use of Brevundimonas efl Access no. DPS RE RSCIC 24 for biocellulose production.
- Still another object of the present invention is a process for biocellulose production including the following steps: a) incubation of Brevundimonas efl Access no. DPS RE RSCIC 24 at room temperature in the presence of culture medium suitable for bacterial growth until obtaining adequate bacterial growth;
- RECTIFIED SHEET (RULE 91) ISA/EP b ) dilution of the culture obtained at the end of step a ) with water and addition of glucose or fructose in an amount ranging between 1 . 5 and 2% of the total and subsequent incubation at room temperature until production of biocellulose by the bacterial culture .
- a further obj ect of the present invention is biocellulose obtained by means of the above process .
- Figure 1 shows a representative infrared spectroscopy (FTIR) spectrum of the materials obtained in static or stirring mode with both bacteria : the spectrum indicates that the material in question is cellulose .
- FTIR infrared spectroscopy
- Figure 2 shows a reference spectrum from Yim, S . M . ; Song, J . E . , Kim, H . R . Production and characterization of bacterial cellulose fabrics by nitrogen sources of tea and carbon sources of sugar, Process Biochemistry 2017 , 59 , 26-36
- biocellulose means cellulose of natural , microbial origin characterised by fibres having variable diameter .
- culture medium suitable for bacterial growth means solid or liquid solutions containing nutrients on which bacterial colonies are possible .
- the obj ect of the present invention is Brevundimonas efl Access n .
- DPS RE RSCIC 24 The obj ect of the present invention is Brevundimonas efl Access n .
- a further obj ect of the present invention is the use of Brevundimonas efl Access n .
- Another another obj ect of the present invention is a process for biocellulose production including the following steps : a ) incubation of Brevundimonas efl Access n . DPS RE RSCIC 24 at room temperature in the presence of culture medium suitable for bacterial growth until obtaining adequate bacterial growth; b ) dilution of the culture obtained at the end of step a ) with water, addition of glucose or fructose in an amount ranging between 1 . 5 and 2% of the total and subsequent incubation at room temperature until production of biocellulose by the bacterial culture .
- step a Brevundimonas ef l Access no .
- DPS RE RSCIC 24 is in combination with Bacillus ef l Access no .
- DPS RE RSCIC 23 is optionally in step a .
- a further obj ect of the present invention is biocellulose of bacterial origin obtained by a process comprising the following steps : a ) incubation of Brevundimonas ef l Access n . DPS RE RSCIC 24 at room temperature in the presence of culture medium suitable for bacterial growth until obtaining adequate bacterial growth; b ) dilution of the culture obtained at the end of step a ) with water and addition of glucose or fructose in an amount ranging between 1 . 5 and 2% of the total and subsequent incubation at room temperature until production of biocellulose by the bacterial culture .
- the obj ect of the present invention is also the use of biocellulose of bacterial origin obtained by a process comprising the following steps : a ) incubation of Brevundimonas efl Access n . DPS RE RSCIC 24 at room temperature in the presence of culture medium suitable for bacterial growth until obtaining adequate bacterial growth; b ) dilution of the culture obtained at the end of step a ) with water and addition of glucose or fructose in an amount ranging between 1 . 5 and 2% of the total and subsequent incubation at room temperature until production of biocellulose by the bacterial culture for the absorption of antibiotics and the subsequent slow release thereof into the environment .
- a further object of the present invention is the use of biocellulose of bacterial origin obtained by a process comprising the following steps : a) incubation of Brevundimonas efl Access n. DPS RE RSCIC 24 at room temperature in the presence of culture medium suitable for bacterial growth until obtaining adequate bacterial growth; b) dilution of the culture obtained at the end of step a) with water and addition of glucose or fructose in an amount ranging between 1.5 and 2% of the total and subsequent incubation at room temperature until production of biocellulose by the bacterial culture for the production of biocellulose filters.
- step a) Brevundimonas efl Access no.
- DPS RE RSCIC 24 is in combination with Bacillus efl Access no.
- DPS RE RSCIC 23 is optionally in step a) Brevundimonas efl Access no.
- the filters can be used in air conditioning or water filtration systems, for example in swimming pools and/or aquariums to block bacterial growth and maintain a healthy environment .
- the biocellulose spheres contain silver nanoparticles with antimicrobial activity.
- the bacterial culture medium can be selected from the group consisting of: Hestrin-Schramm, Yamanaka, Zhou, nutrient broth or yeast extract .
- yeast extract is yeast extract (0.5-1%) .
- the water is seawater or deionised water.
- the nutrient broth has the following composition:
- step a) and step b) the bacteria are incubated at a temperature ranging from 22 and 25 °C.
- step a) the bacteria are incubated statically or under stirring .
- the bacteria When in step a) the bacteria are incubated under stirring, they are preferably under stirring by means of a stirrer at a speed of about 150-200 rpm.
- the adequate bacterial growth is the achievement of an optical density of about 0.6 OD at 550 nanometres.
- step b) if the water is seawater in an amount equal to
- step b) if the water is deionised water it is in an amount equal to 90 % of the final volume.
- step b) glucose or fructose is present in an amount equal to 1.5%.
- the temperature is 22 °C.
- the obtained biocellulose is in the form of a sheet when in step a) the incubation is in static mode.
- the obtained biocellulose is in the form of spheres when in step a) the incubation is under stirring and preferably they have an average diameter ranging between 2 and 10 mm.
- the first strain Bacillus efl Access no. DPS RE RSCIC 23 was identified as belonging to the genus Bacillus on the basis of the 16S rDNA sequence, it is similar to Bacillus altitudinis, it is a gram-positive rod-shaped bacterium. SEQ ID . NO . 1 PRQKKA_03858 Bacillus 16S ribosomal RNA
- DPS RE RSCIC 24 was identified as belonging to the genus Brevundimonas on the basis of the 16S rDNA sequence
- DPS RE RSCIC 24 is similar to Brevundimonas vesicularis adapted to live in Martian conditions .
- sequences similar to the 16S rRNA gene there is one from the strain Brevundimonas sp . R-37024 isolated from a Lake Lundstrdm in Antarctica .
- Brevundimonas ef l possesses an enzyme involved in cellulose biosynthesis .
- the nutrient broth had the following composition:
- Yeast extract is a source of vitamins, particularly B group vitamins. Sodium chloride maintains the osmotic balance of the medium.
- the bacteria incubated at 22°C at 150-200 rpm of rotation.
- the culture is diluted with seawater H 2 0 (50 % of the final volume) or deionised water (90 % of the final volume) . and added with 1.5-2% glucose, and further incubated statically (without stirring) or with stirring at 22°C.
- biocellulose sheet is produced (static mode)
- biocellulose spheres are produced (stirring mode) by Bacillus efl Access no. DPS RE RSCIC 23 in nutrient broth diluted with 50% seawater and added with 1.5-2%.
- biocellulose sheet is produced (static mode)
- biocellulose spheres are produced (stirring mode) by Brevundimonas efl Access no.
- DPS RE RSCIC 24 of 25/11/2020 both cultivated in nutrient broth and in yeast extract occurs .
- biocellulose spheres The ability of the biocellulose spheres to absorb external substances as previously produced was further tested .
- Methylene blue is partially released into the culture medium: after 18 hours , about l/20th of the initial amount absorbed is released .
- Table 2 reports the production methods ( rotation speed, medium volume , flask size ) , yield and average size of the biocellulose spheres synthesised by Bacillus ef l and Brevundimonas efl after 5 days of culture .
- the biocellulose in the form of spheres was also soaked in a solution containing silver nanoparticles ( 20 mg/ml ) having antimicrobial activity, as described in the application incorporated herein for Italian patent reference no . 102019000014121 by the same inventors , 24 hours and subj ected to UV ray sterilisation for 10 minutes . Then the biocellulose spheres were placed in a plate with Muller hinton agar where a strain of Candida albicans was inoculated . The growth inhibitory effect of Candida was visible with a halo of about 4-5 mm even after 72 hours at 22 ° C .
Landscapes
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Zoology (AREA)
- Wood Science & Technology (AREA)
- Genetics & Genomics (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Microbiology (AREA)
- Biochemistry (AREA)
- General Health & Medical Sciences (AREA)
- Biomedical Technology (AREA)
- Medicinal Chemistry (AREA)
- Virology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Molecular Biology (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IT102020000031769A IT202000031769A1 (it) | 2020-12-22 | 2020-12-22 | Ceppi batterici per la produzione di biocellulosa |
| PCT/EP2021/086800 WO2022136277A1 (fr) | 2020-12-22 | 2021-12-20 | Souches bactériennes pour la production de biocellulose |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| EP4267721A1 true EP4267721A1 (fr) | 2023-11-01 |
Family
ID=74875088
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP21824606.4A Pending EP4267720A1 (fr) | 2020-12-22 | 2021-12-20 | Souches bactériennes pour la production de biocellulose |
| EP21840612.2A Pending EP4267721A1 (fr) | 2020-12-22 | 2021-12-20 | Souches bactériennes pour la production de biocellulose |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP21824606.4A Pending EP4267720A1 (fr) | 2020-12-22 | 2021-12-20 | Souches bactériennes pour la production de biocellulose |
Country Status (4)
| Country | Link |
|---|---|
| EP (2) | EP4267720A1 (fr) |
| KR (2) | KR20230124918A (fr) |
| IT (1) | IT202000031769A1 (fr) |
| WO (2) | WO2022136277A1 (fr) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| IT202100017333A1 (it) * | 2021-07-01 | 2023-01-01 | Irides S R L | Produzione di biomateriali da prodotti di scarto alimentari da parte di ceppi batterici antartici |
| CN118207137A (zh) * | 2024-04-17 | 2024-06-18 | 江西农业大学 | 一种高效纤维素降解菌剂及其制备方法和应用 |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR691410A (fr) | 1930-03-03 | 1930-10-21 | Jeu de direction indéréglable pour cycles, motocycles, etc. | |
| IT201900014121A1 (it) | 2019-08-06 | 2021-02-06 | Univ Degli Studi Di Camerino | Marinomonas ef1 e rhodococcus ef1 per la produzione di metaboliti secondari |
-
2020
- 2020-12-22 IT IT102020000031769A patent/IT202000031769A1/it unknown
-
2021
- 2021-12-20 WO PCT/EP2021/086800 patent/WO2022136277A1/fr not_active Ceased
- 2021-12-20 KR KR1020237021057A patent/KR20230124918A/ko active Pending
- 2021-12-20 WO PCT/EP2021/086747 patent/WO2022136246A1/fr not_active Ceased
- 2021-12-20 EP EP21824606.4A patent/EP4267720A1/fr active Pending
- 2021-12-20 EP EP21840612.2A patent/EP4267721A1/fr active Pending
- 2021-12-20 KR KR1020237021058A patent/KR20230124919A/ko active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| IT202000031769A1 (it) | 2022-06-22 |
| KR20230124919A (ko) | 2023-08-28 |
| KR20230124918A (ko) | 2023-08-28 |
| WO2022136277A1 (fr) | 2022-06-30 |
| EP4267720A1 (fr) | 2023-11-01 |
| WO2022136246A1 (fr) | 2022-06-30 |
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