JPWO2020037270A5 - - Google Patents

Download PDF

Info

Publication number
JPWO2020037270A5
JPWO2020037270A5 JP2021507742A JP2021507742A JPWO2020037270A5 JP WO2020037270 A5 JPWO2020037270 A5 JP WO2020037270A5 JP 2021507742 A JP2021507742 A JP 2021507742A JP 2021507742 A JP2021507742 A JP 2021507742A JP WO2020037270 A5 JPWO2020037270 A5 JP WO2020037270A5
Authority
JP
Japan
Prior art keywords
pectin
amidated
nucleic acid
modified
amidated pectin
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.)
Granted
Application number
JP2021507742A
Other languages
Japanese (ja)
Other versions
JP7431217B2 (en
JP2021533776A (en
Publication date
Application filed filed Critical
Priority claimed from PCT/US2019/046925 external-priority patent/WO2020037270A1/en
Publication of JP2021533776A publication Critical patent/JP2021533776A/en
Publication of JPWO2020037270A5 publication Critical patent/JPWO2020037270A5/ja
Application granted granted Critical
Publication of JP7431217B2 publication Critical patent/JP7431217B2/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Claims (21)

表面上の核酸コンタミネーションを低減する方法であって、
核酸でコンタミネーションされた表面を、修飾ペクチンを含む組成物と接触させる工程を含み、
前記修飾ペクチンは複数のアミノ基を含
前記修飾ペクチンは式
Figure 2020037270000001
その互変異性体、異性体、又は塩で表される1つ以上のモノマー単位を含む、アミド化ペクチンであり、
ここで、nは、0、1、2、又は3であり、
R 1 は、H又はC 1 -C 3 アルキルであり、
Xは、各出現において、独立してC 2 -C 4 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、
Yは、C 2 -C 3 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、及び
R 2 及びR 3 は、独立して、H又はC 1 -C 3 アルキルである、
方法。
A method of reducing nucleic acid contamination on a surface comprising:
contacting the nucleic acid-contaminated surface with a composition comprising modified pectin;
The modified pectin contains a plurality of amino groups,
Said modified pectin has the formula
Figure 2020037270000001
an amidated pectin comprising one or more monomeric units represented by its tautomers, isomers or salts;
where n is 0, 1, 2, or 3;
R 1 is H or C 1 -C 3 alkyl,
X at each occurrence is independently C2 - C4 alkylene or C4 - C6 heteroalkylene;
Y is C2 - C3 alkylene or C4 - C6 heteroalkylene , and
R2 and R3 are independently H or C1 - C3 alkyl ;
Method.
前記アミド化ペクチンの分子量が約0.5kDa~約500kDaの間である、請求項1の方法。 2. The method of claim 1 , wherein said amidated pectin has a molecular weight between about 0.5 kDa and about 500 kDa. 前記アミド化ペクチンの分子量が約100kDa~約300kDaである、請求項1の方法。 2. The method of claim 1 , wherein the amidated pectin has a molecular weight of about 100 kDa to about 300 kDa. 前記アミド化ペクチンを含む組成物が前記アミド化ペクチンの溶液である、請求項1の方法。 2. The method of claim 1 , wherein the composition comprising said amidated pectin is a solution of said amidated pectin. 前記アミド化ペクチンが約0.01%~約5%の濃度で溶液中に存在する、請求項4の方法。 5. The method of claim 4 , wherein said amidated pectin is present in solution at a concentration of about 0.01% to about 5%. 前記アミド化ペクチンが約0.1%~約0.5%の濃度で溶液中に存在する、請求項4の方法。 5. The method of claim 4 , wherein said amidated pectin is present in solution at a concentration of about 0.1% to about 0.5%. 前記アミド化ペクチンが約1ug/mL~約1000ug/mLの濃度で溶液中に存在する、請求項4の方法。 5. The method of claim 4 , wherein said amidated pectin is present in solution at a concentration of about 1 ug/mL to about 1000 ug/mL. 前記アミド化ペクチンがアミド化シトラスペクチン又はアミド化リンゴペクチンである、請求項1の方法。 2. The method of claim 1 , wherein said amidated pectin is amidated citrus pectin or amidated apple pectin. 前記組成物がスワブ、ワイプ、クロス、フィルター、又はスポンジ上に存在する、請求項1の方法。 2. The method of Claim 1 , wherein the composition is present on a swab, wipe, cloth, filter, or sponge. 前記表面が器具の表面又は実験台の表面である、請求項1の方法。 2. The method of claim 1 , wherein the surface is an instrument surface or a laboratory bench surface. 溶液中の核酸コンタミネーションを低減する方法であって、
核酸でコンタミネーションされた溶液を、固体支持体に共有結合した修飾ペクチンを含む固体支持体と接触させる工程を含み、
前記修飾ペクチンは複数のアミノ基を含
前記修飾ペクチンは式
Figure 2020037270000002
その互変異性体、異性体、又は塩で表される1つ以上のモノマー単位を含む、アミド化ペクチンであり、
ここで、nは、0、1、2、又は3であり、
R 1 は、H又はC 1 -C 3 アルキルであり、
Xは、各出現において、独立して、C 2 -C 4 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、
Yは、C 2 -C 3 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、及び
R 2 及びR 3 は、独立して、H又はC 1 -C 3 アルキルである、
方法。
A method of reducing nucleic acid contamination in a solution, comprising:
contacting the nucleic acid-contaminated solution with a solid support comprising modified pectin covalently attached to the solid support;
The modified pectin contains a plurality of amino groups,
Said modified pectin has the formula
Figure 2020037270000002
an amidated pectin comprising one or more monomeric units represented by its tautomers, isomers or salts;
where n is 0, 1, 2, or 3;
R 1 is H or C 1 -C 3 alkyl,
X, at each occurrence, is independently C2 - C4 alkylene or C4 - C6 heteroalkylene;
Y is C2 - C3 alkylene or C4 - C6 heteroalkylene , and
R2 and R3 are independently H or C1 - C3 alkyl ;
Method.
前記固体支持体が磁性ビーズ、ガラスビーズ、ポリスチレンビーズ、ポリスチレンフィルター、又はガラスフィルターである、請求項11の方法。 12. The method of claim 11 , wherein said solid support is magnetic beads, glass beads, polystyrene beads, polystyrene filters, or glass filters. 前記固体支持体がスワブ、ワイプ、クロス、フィルター、又はスポンジである、請求項11の方法。 12. The method of Claim 11 , wherein said solid support is a swab, wipe, cloth, filter, or sponge. 空気中のエアロゾル化核酸コンタミネーションを低減する方法であって、
エアロゾル化核酸でコンタミネーションされた空気を、修飾ペクチンを含む組成物と接触させる工程を含み、
前記修飾ペクチンが複数のアミノ基を含
前記修飾ペクチンは式
Figure 2020037270000003
その互変異性体、異性体、又は塩で表される1つ以上のモノマー単位を含む、アミド化ペクチンであり、
ここで、nは、0、1、2、又は3であり、
R 1 は、H又はC 1 -C 3 アルキルであり、
Xは、各出現において、独立して、C 2 -C 4 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、
Yは、C 2 -C 3 アルキレン又はC 4 -C 6 ヘテロアルキレンであり、及び
R 2 及びR 3 は、独立して、H又はC 1 -C 3 アルキルである、
方法。
A method of reducing aerosolized nucleic acid contamination in the air comprising:
contacting air contaminated with aerosolized nucleic acid with a composition comprising modified pectin;
The modified pectin contains a plurality of amino groups,
Said modified pectin has the formula
Figure 2020037270000003
an amidated pectin comprising one or more monomeric units represented by its tautomers, isomers or salts;
where n is 0, 1, 2, or 3;
R 1 is H or C 1 -C 3 alkyl,
X, at each occurrence, is independently C2 - C4 alkylene or C4 - C6 heteroalkylene;
Y is C2 - C3 alkylene or C4 - C6 heteroalkylene , and
R2 and R3 are independently H or C1 - C3 alkyl ;
Method.
エアロゾル化核酸でコンタミネーションされた空気を接触させる工程が、アミド化ペクチンを含む溶液に空気を通す工程を含む、請求項14の方法。 15. The method of claim 14 , wherein contacting air contaminated with aerosolized nucleic acid comprises passing air through a solution comprising amidated pectin. エアロゾル化核酸でコンタミネーションされた空気を接触させる工程が、アミド化ペクチンを含むフィルターに空気を通す工程を含む、請求項14の方法。 15. The method of claim 14 , wherein contacting air contaminated with aerosolized nucleic acid comprises passing the air through a filter containing amidated pectin. 前記アミド化ペクチンが前記フィルターに共有結合している、請求項16の方法。 17. The method of claim 16 , wherein said amidated pectin is covalently attached to said filter. エアロゾル化核酸でコンタミネーションされた空気を接触させる工程が、表面に共有結合したアミド化ペクチンを含む表面の上に空気を通す工程を含む、請求項14の方法。 15. The method of claim 14, wherein contacting air contaminated with aerosolized nucleic acid comprises passing air over a surface comprising amidated pectin covalently bound to the surface. 前記核酸が核酸増幅反応の産物である、請求項1~18のいずれか1項の方法。 19. The method of any one of claims 1-18 , wherein said nucleic acid is the product of a nucleic acid amplification reaction. 前記増幅反応がポリメラーゼ連鎖反応である、請求項19の方法。 20. The method of claim 19 , wherein said amplification reaction is the polymerase chain reaction. 前記修飾ペクチンが、式
Figure 2020037270000004
又はそれらの異性体、塩、又は互変異性体で表される1つ以上のモノマー単位を含むアミド化ペクチンである、請求項1~20のいずれか1項の方法。
wherein the modified pectin has the formula
Figure 2020037270000004
or an amidated pectin comprising one or more monomeric units represented by their isomers, salts or tautomers.
JP2021507742A 2018-08-17 2019-08-16 Nucleic acid decontamination method Active JP7431217B2 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862765014P 2018-08-17 2018-08-17
US62/765,014 2018-08-17
PCT/US2019/046925 WO2020037270A1 (en) 2018-08-17 2019-08-16 Nucleic acid decontamination methods

Publications (3)

Publication Number Publication Date
JP2021533776A JP2021533776A (en) 2021-12-09
JPWO2020037270A5 true JPWO2020037270A5 (en) 2022-08-23
JP7431217B2 JP7431217B2 (en) 2024-02-14

Family

ID=67909453

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2021507742A Active JP7431217B2 (en) 2018-08-17 2019-08-16 Nucleic acid decontamination method

Country Status (8)

Country Link
US (1) US11819584B2 (en)
EP (1) EP3836975A1 (en)
JP (1) JP7431217B2 (en)
KR (1) KR20210045453A (en)
CN (1) CN113056291B (en)
AU (1) AU2019320827A1 (en)
CA (1) CA3109795A1 (en)
WO (1) WO2020037270A1 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114672482B (en) * 2022-05-31 2022-08-30 上海百力格生物技术有限公司 Method for preparing nucleic acid probe

Family Cites Families (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IT1264321B (en) * 1992-01-13 1996-09-23 Mini Ricerca Scient Tecnolog ESTERS OF PECTIC AND PECTINIC ACIDS, PREPARATION PROCEDURE AND THEIR PHARMACEUTICAL AND BIOSANITARY APPLICATIONS
PL314522A1 (en) * 1993-11-23 1996-09-16 Ciba Corning Diagnostics Corp Application of antisense oligomers in a contamination controlling process during nucleic acids amplification reactions
WO2002090386A2 (en) * 2001-05-04 2002-11-14 Ato B.V. Regulatory protein involved in pectin modification
DK176653B1 (en) * 2002-07-02 2009-02-02 Cp Kelco Aps Process for the preparation of low esterification amidated pectin, amidated pectin obtainable by the process and use thereof
MXPA05010681A (en) * 2003-04-04 2005-12-15 Diversa Corp Pectate lyases, nucleic acids encoding them and methods for making and using them.
CN1798570A (en) * 2003-04-07 2006-07-05 坎巴斯有限公司 Anti-fungal compounds and methods of use
US7125842B2 (en) * 2003-04-07 2006-10-24 Canbas Co. Ltd. Anti-fungal compounds and methods of use
WO2005056782A2 (en) * 2003-12-03 2005-06-23 Genencor International, Inc. Perhydrolase
US20050163825A1 (en) * 2004-01-27 2005-07-28 Naidu A. S. Lactoferrin-treated filament materials
ES2353527T3 (en) * 2004-12-09 2011-03-02 The Dial Corporation COMPOSITIONS THAT HAVE A HIGH ANTIVIRAL AND ANTIBACTERIAL EFFECT.
US8580192B2 (en) * 2006-10-31 2013-11-12 Ethicon, Inc. Sterilization of polymeric materials
DE102008063003A1 (en) 2008-12-23 2010-06-24 Qiagen Gmbh Nucleic acid purification method
AU2015201538A1 (en) * 2009-03-04 2015-04-16 Trustees Of Tufts College Silk fibroin systems for antibiotic delivery
US8039613B2 (en) * 2009-08-28 2011-10-18 Promega Corporation Methods of purifying a nucleic acid and formulation and kit for use in performing such methods
US8716176B2 (en) * 2011-09-19 2014-05-06 Cp Kelco Aps Low soluble solids acid gels and methods for making same
CN105683394A (en) * 2013-09-30 2016-06-15 南方花园橙业公司 A method for assessing juice/cider quality and/or safety
JP2015119656A (en) 2013-12-24 2015-07-02 東洋紡株式会社 Nucleic acid amplification technique
EP3227419B1 (en) * 2014-12-05 2019-08-14 Dalli-Werke GmbH & Co. KG. Pectin comprising effervescent compositions
CN108219026A (en) * 2016-12-14 2018-06-29 杭州垚信生物科技有限公司 A kind of preparation method of high gelling beet pectin
CN107141369B (en) 2017-05-25 2019-10-18 华南理工大学 A kind of preparation method of modified pectin

Similar Documents

Publication Publication Date Title
KR102292139B1 (en) Ion complex material having function of inhibiting adhesion of biological matter and production method for same
EP3013146B1 (en) Wipe with a guanidinyl-containing polymer
US10450333B2 (en) Guanidine-functionalized particles and methods of making and using
US9556340B2 (en) Polyoxazoline copolymers
EP1702990A1 (en) Composition and method for array hybridization
Monserud et al. Effects of molecular size and surface hydrophobicity on oligonucleotide interfacial dynamics
JP4969760B2 (en) polymer
Eginton et al. The influence of substratum properties on the attachment of bacterial cells
CN101568557A (en) Surface-bound fluorinated esters for amine capture
RU2014124190A (en) LONG RIGID SPACERS TO IMPROVE BINDING KINETICS IN IMMUNO ANALYSIS
EP1715039A1 (en) Method of isolating a nucleic acid using a bifunctional material containing an amino group and a carboxyl group
Öberg et al. Synthesis, biological evaluation, and structure–activity relationships of 2-[2-(benzoylamino) benzoylamino] benzoic acid analogues as inhibitors of adenovirus replication
JP2020500948A5 (en)
US7671154B2 (en) Crosslinked polymers with amine binding groups
KR20080047431A (en) Crosslinked polymers with amine binding groups
JPWO2020037270A5 (en)
CN105566587B (en) A kind of preparation method and applications of polyvinyl alcohol diazonium polymer
EP3719113A1 (en) Cell culture container capable of long-term culture, and method for manufacturing same
US20070190537A1 (en) Solid phase synthesis
WO2021167037A1 (en) Adhesion inhibitor for biomaterials
US9310358B2 (en) Sugar chain array
Silva et al. Lysozyme binding to poly (4-vinyl-N-alkylpyridinium bromide)
KR100981289B1 (en) Peptide nucleic acid oligomers comprising universal bases, preparation methods thereof, and kits, devices and methods for the analysis, detection or modulation of nucleic acids using the same
WO2015133461A1 (en) Ion complex material having function for preventing adherence to biological material
WO2020166605A1 (en) Method for producing polymer compatible with biomaterials