CN113736815A - 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 - Google Patents
一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 Download PDFInfo
- Publication number
- CN113736815A CN113736815A CN202111035771.0A CN202111035771A CN113736815A CN 113736815 A CN113736815 A CN 113736815A CN 202111035771 A CN202111035771 A CN 202111035771A CN 113736815 A CN113736815 A CN 113736815A
- Authority
- CN
- China
- Prior art keywords
- bacillus subtilis
- strain
- recombinant
- floa
- yield
- 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
Links
- 244000063299 Bacillus subtilis Species 0.000 title claims abstract description 46
- 235000014469 Bacillus subtilis Nutrition 0.000 title claims abstract description 46
- MJVAVZPDRWSRRC-UHFFFAOYSA-N Menadione Chemical compound C1=CC=C2C(=O)C(C)=CC(=O)C2=C1 MJVAVZPDRWSRRC-UHFFFAOYSA-N 0.000 title claims abstract description 18
- 210000002284 membrane microdomain Anatomy 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims abstract description 12
- 238000005728 strengthening Methods 0.000 title claims abstract description 9
- 229940041603 vitamin k 3 Drugs 0.000 title claims abstract description 9
- 235000012711 vitamin K3 Nutrition 0.000 title claims abstract description 8
- 239000011652 vitamin K3 Substances 0.000 title claims abstract description 8
- ZGEGCLOFRBLKSE-UHFFFAOYSA-N 1-Heptene Chemical compound CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 title claims description 7
- 238000000855 fermentation Methods 0.000 claims abstract description 22
- 230000004151 fermentation Effects 0.000 claims abstract description 22
- 101710167800 Capsid assembly scaffolding protein Proteins 0.000 claims abstract description 11
- 101710130420 Probable capsid assembly scaffolding protein Proteins 0.000 claims abstract description 11
- 101710204410 Scaffold protein Proteins 0.000 claims abstract description 11
- 108090000623 proteins and genes Proteins 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 6
- 239000001963 growth medium Substances 0.000 claims description 7
- 230000002708 enhancing effect Effects 0.000 claims description 4
- 239000002773 nucleotide Substances 0.000 claims description 4
- 125000003729 nucleotide group Chemical group 0.000 claims description 4
- 238000011218 seed culture Methods 0.000 claims description 3
- PFRQBZFETXBLTP-UHFFFAOYSA-N Vitamin K2 Natural products C1=CC=C2C(=O)C(CC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)CCC=C(C)C)=C(C)C(=O)C2=C1 PFRQBZFETXBLTP-UHFFFAOYSA-N 0.000 abstract description 22
- 235000009464 menaquinone-7 Nutrition 0.000 abstract description 22
- 239000011700 menaquinone-7 Substances 0.000 abstract description 22
- RAKQPZMEYJZGPI-LJWNYQGCSA-N menaquinone-7 Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 RAKQPZMEYJZGPI-LJWNYQGCSA-N 0.000 abstract description 22
- 101710171204 30S ribosomal protein S20 Proteins 0.000 abstract description 13
- 230000001965 increasing effect Effects 0.000 abstract description 8
- 210000000170 cell membrane Anatomy 0.000 abstract description 5
- 230000001976 improved effect Effects 0.000 abstract description 3
- 102000004169 proteins and genes Human genes 0.000 abstract description 3
- 238000004680 force modulation microscopy Methods 0.000 abstract 1
- 101100013156 Bacillus subtilis (strain 168) floT gene Proteins 0.000 description 7
- 229960005091 chloramphenicol Drugs 0.000 description 7
- WIIZWVCIJKGZOK-RKDXNWHRSA-N chloramphenicol Chemical compound ClC(Cl)C(=O)N[C@H](CO)[C@H](O)C1=CC=C([N+]([O-])=O)C=C1 WIIZWVCIJKGZOK-RKDXNWHRSA-N 0.000 description 7
- 239000013612 plasmid Substances 0.000 description 6
- 101150071609 floA gene Proteins 0.000 description 5
- 238000012216 screening Methods 0.000 description 5
- 230000004927 fusion Effects 0.000 description 4
- 230000010354 integration Effects 0.000 description 4
- 239000002609 medium Substances 0.000 description 4
- 238000011144 upstream manufacturing Methods 0.000 description 4
- 238000012795 verification Methods 0.000 description 4
- YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- 230000003115 biocidal effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000012634 fragment Substances 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 239000001888 Peptone Substances 0.000 description 2
- 108010080698 Peptones Proteins 0.000 description 2
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 2
- 229930003448 Vitamin K Natural products 0.000 description 2
- 230000003321 amplification Effects 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 238000010276 construction Methods 0.000 description 2
- 238000001514 detection method Methods 0.000 description 2
- 238000004128 high performance liquid chromatography Methods 0.000 description 2
- BPHPUYQFMNQIOC-NXRLNHOXSA-N isopropyl beta-D-thiogalactopyranoside Chemical compound CC(C)S[C@@H]1O[C@H](CO)[C@H](O)[C@H](O)[C@H]1O BPHPUYQFMNQIOC-NXRLNHOXSA-N 0.000 description 2
- 229930027917 kanamycin Natural products 0.000 description 2
- 229960000318 kanamycin Drugs 0.000 description 2
- SBUJHOSQTJFQJX-NOAMYHISSA-N kanamycin Chemical compound O[C@@H]1[C@@H](O)[C@H](O)[C@@H](CN)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O[C@@H]2[C@@H]([C@@H](N)[C@H](O)[C@@H](CO)O2)O)[C@H](N)C[C@@H]1N SBUJHOSQTJFQJX-NOAMYHISSA-N 0.000 description 2
- 229930182823 kanamycin A Natural products 0.000 description 2
- 239000012528 membrane Substances 0.000 description 2
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 2
- 238000003199 nucleic acid amplification method Methods 0.000 description 2
- 235000019319 peptone Nutrition 0.000 description 2
- SHUZOJHMOBOZST-UHFFFAOYSA-N phylloquinone Natural products CC(C)CCCCC(C)CCC(C)CCCC(=CCC1=C(C)C(=O)c2ccccc2C1=O)C SHUZOJHMOBOZST-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 238000012163 sequencing technique Methods 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 235000019168 vitamin K Nutrition 0.000 description 2
- 239000011712 vitamin K Substances 0.000 description 2
- 150000003721 vitamin K derivatives Chemical class 0.000 description 2
- 229940046010 vitamin k Drugs 0.000 description 2
- HYPYXGZDOYTYDR-HAJWAVTHSA-N 2-methyl-3-[(2e,6e,10e,14e)-3,7,11,15,19-pentamethylicosa-2,6,10,14,18-pentaenyl]naphthalene-1,4-dione Chemical compound C1=CC=C2C(=O)C(C/C=C(C)/CC/C=C(C)/CC/C=C(C)/CC/C=C(C)/CCC=C(C)C)=C(C)C(=O)C2=C1 HYPYXGZDOYTYDR-HAJWAVTHSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- 244000068988 Glycine max Species 0.000 description 1
- 235000010469 Glycine max Nutrition 0.000 description 1
- 239000012880 LB liquid culture medium Substances 0.000 description 1
- 208000001132 Osteoporosis Diseases 0.000 description 1
- 240000004808 Saccharomyces cerevisiae Species 0.000 description 1
- 208000034189 Sclerosis Diseases 0.000 description 1
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- 229930182558 Sterol Natural products 0.000 description 1
- 238000002835 absorbance Methods 0.000 description 1
- 230000003213 activating effect Effects 0.000 description 1
- 230000001580 bacterial effect Effects 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 230000023555 blood coagulation Effects 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 238000012258 culturing Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 230000002526 effect on cardiovascular system Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000000605 extraction Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 235000013376 functional food Nutrition 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 238000011081 inoculation Methods 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 150000002632 lipids Chemical class 0.000 description 1
- 230000002503 metabolic effect Effects 0.000 description 1
- 230000004060 metabolic process Effects 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- 238000007857 nested PCR Methods 0.000 description 1
- 238000006384 oligomerization reaction Methods 0.000 description 1
- 230000003287 optical effect Effects 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- PJNZPQUBCPKICU-UHFFFAOYSA-N phosphoric acid;potassium Chemical compound [K].OP(O)(O)=O PJNZPQUBCPKICU-UHFFFAOYSA-N 0.000 description 1
- 229920001195 polyisoprene Polymers 0.000 description 1
- 230000008092 positive effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001243 protein synthesis Methods 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000008223 sterile water Substances 0.000 description 1
- 150000003432 sterols Chemical class 0.000 description 1
- 235000003702 sterols Nutrition 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 235000019143 vitamin K2 Nutrition 0.000 description 1
- 239000011728 vitamin K2 Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Chemical compound O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 101150063388 yqfB gene Proteins 0.000 description 1
Images
Classifications
-
- 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
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/63—Introduction of foreign genetic material using vectors; Vectors; Use of hosts therefor; Regulation of expression
- C12N15/74—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora
- C12N15/75—Vectors or expression systems specially adapted for prokaryotic hosts other than E. coli, e.g. Lactobacillus, Micromonospora for Bacillus
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K14/00—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- C07K14/195—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria
- C07K14/32—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from bacteria from Bacillus (G)
-
- 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
- C12P7/00—Preparation of oxygen-containing organic compounds
- C12P7/66—Preparation of oxygen-containing organic compounds containing the quinoid structure
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Genetics & Genomics (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- General Health & Medical Sciences (AREA)
- Biotechnology (AREA)
- General Engineering & Computer Science (AREA)
- Biochemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Biophysics (AREA)
- Microbiology (AREA)
- Molecular Biology (AREA)
- Biomedical Technology (AREA)
- Plant Pathology (AREA)
- Physics & Mathematics (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Gastroenterology & Hepatology (AREA)
- Medicinal Chemistry (AREA)
- Proteomics, Peptides & Aminoacids (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
Abstract
本发明公开了一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法,本发明的方法是通过强化表达产七烯甲萘醌的枯草芽孢杆菌功能膜微域中的脚手架蛋白FloA。本发明通过对已高产MK‑7的重组枯草芽孢杆菌BS20中的脚手架蛋白使用强启动子P43进行强化,增加FMMs在细胞质膜上的占比后,进一步提高了MK‑7的产量,与对照菌株BS20相比,强化FloA的重组枯草芽孢杆菌BSQ1产量最高,发酵6天后,BSQ1菌株产量达到417.08mg/L,较BS20菌株提升了16.57%。
Description
技术领域
本发明涉及一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法,属于代谢技术领域。
背景技术
维生素K作为一类重要的脂溶性维生素,是人体不可缺少的重要维生素之一,在加速凝血、预防心血管硬化和治疗骨质疏松等方面起着关键作用。维生素K以2-甲基-1,4-萘醌为骨架,根据C3位支链结构的不同,可将维生素K分成不同的亚型。其中七烯甲萘醌(Menaquinone-7,MK-7)由于具有在人体中半衰期长、亲缘性高等特点,目前在功能性食品和医药等领域备受关注。发明人课题组前期申请的中国专利目CN110157749B已在枯草芽孢杆菌中达到了较高MK-7产量,但是在研究中发现常规的代谢改造,如强化合成途径、阻断副产物的形成等,很难进一步提高MK-7的产量。
功能膜微域(Functional Membrane Microdomains,FMMs)是细菌细胞脂膜上富含固醇类似物聚异戊二烯化合物的一类结构致密性微域,并且富含特殊的脚手架蛋白。这类脚手架蛋白作为一种膜结合伴侣蛋白,仅定位在FMMs上,可以招募需要定位在FMMs上的蛋白并促进这些蛋白的相互作用以及寡聚化,在组织和形成FMMs的过程中起到重要作用。目前还没有研究表明是否能够通过对枯草芽孢杆菌中的FMMs进行强化,增加FMMs在细胞质膜中的占比,增加MK-7在细胞质膜上的存储空间以提高MK-7的产量。
发明内容
为解决上述技术问题,本发明通过对FMMs中的FloA、FloT蛋白进行强化,增加FMMs在细胞质膜上的占比后,进一步提高了MK-7的产量。
本发明的第一个目的是提供一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法,所述方法是通过强化表达产七烯甲萘醌的枯草芽孢杆菌功能膜微域中的脚手架蛋白FloA。
进一步地,所述的强化表达是通过使用强启动子进行强化表达。
进一步地,所述的强启动子为P43启动子。
本发明的第二个目的是提供一种产七烯甲萘醌的枯草芽孢杆菌重组菌,所述的枯草芽孢杆菌重组菌是通过强化表达枯草芽孢杆菌宿主功能膜微域中的脚手架蛋白FloA获得。
进一步地,所述的强化表达是通过使用强启动子P43进行强化表达。
进一步地,所述的强启动子P43的核苷酸序列如SEQ ID NO.3所示。
进一步地,所述的枯草芽孢杆菌宿主为枯草芽孢杆菌BS20。枯草芽孢杆菌BS20在专利CN110157749B中公开。
进一步地,所述的脚手架蛋白FloA的编码基因的核苷酸序列如SEQ ID NO.4所示。
本发明的第三个目的是提供所述的枯草芽孢杆菌重组菌在发酵生产七烯甲萘醌中的应用。
进一步地,所述应用具体是将重组枯草芽孢杆菌在种子培养基中活化,然后将活化后的种子转入发酵培养基,进行发酵培养,获得七烯甲萘醌。
本发明的有益效果是:
本发明通过对已高产MK-7的重组枯草芽孢杆菌BS20中的脚手架蛋白使用强启动子P43进行强化,增加FMMs在细胞质膜上的占比后,进一步提高了MK-7的产量,与对照菌株BS20相比,强化FloA的重组枯草芽孢杆菌BSQ1产量最高,发酵6天后,BSQ1菌株产量达到417.08mg/L,较BS20菌株提升了16.57%。
附图说明:
图1为发酵6天后,BS20、BSQ1、BSQ2、BSQ12菌株发酵生产MK-7的产量。
具体实施方式
下面结合具体实施例对本发明作进一步说明,以使本领域的技术人员可以更好地理解本发明并能予以实施,但所举实施例不作为对本发明的限定。
(1)培养基
种子培养基的成分包括:10g/L蛋白胨、5g/L酵母粉和10g/L氯化钠。
发酵培养基的成分包括:50g/L葡萄糖、50g/L甘油、50g/L大豆蛋白胨、0.6g/L磷酸二氢钾。
(2)MK-7萃取剂:异丙醇和正已烷混合物(1:2,V/V)
(3)HPLC检测MK-7产量:采用Agilent ZORBAX EclipseXDB-C18分离柱(5μm,250×4.6mm),检测的温度在40℃,流动相使用甲醇:二氯甲烷(9:1,v/v),流速为1mL/min,检测波长254nm,进样量10μL。
(4)菌株生长情况检测:使用紫外-可见分光光度计定时测定发酵液的吸光光度值OD600。
实施例1:重组枯草芽孢杆菌BSQ1、BSQ2的构建
分别将P43启动子通过cre/loxp系统整合在重组枯草芽孢杆菌BS20基因组上floA(yuaG)和floT(yqfB)的上游,构建重组枯草芽孢杆菌BSQ1和BSQ2,具体构建过程如下。
通过重叠延伸PCR,对以下序列进行片段扩增,P43-floA整合框所需的扩增序列为floA上游序列(长度1000bp,序列如SEQ ID NO.1)、氯霉素抗性基因zeo序列(1309bp,序列如SEQ ID NO.2)、P43启动子(0.3bp,序列如SEQ ID NO.3)和floA序列(996bp,序列如SEQID NO.4)。P43-floT整合框所需的扩增序列为floT上游序列(长度1000bp,序列如SEQ IDNO.5)、氯霉素抗性基因zeo序列(1309bp)、P43启动子(0.3bp)和floT序列(1000bp,序列如SEQ ID NO.6)。引物序列见表1,其中floA-P7C6-1R和floA-P43-1F为两个整合框的通用引物。通过融合PCR获得floAup-lox71-zeo-lox66-p43-floA和floTup-lox71-zeo-lox66-p43-floT融合表达框。
表1
将获得的融合表达框片段通过化学转化的方式整合至重组枯草芽孢杆菌BS20基因组中,整合片段的添加量约为1000ng。通过添加氯霉素抗性的LB固体培养基进行筛选、挑取单菌落进行PCR验证、测序验证,确认整合成功。
对整合成功的重组枯草芽孢杆菌进行氯霉素抗性的消除,通过化学转化的方式将Cre质粒转入构建好的重组枯草芽孢杆菌中,经添加卡纳抗生素的LB固体培养基筛选后,通过IPTG诱导Cre质粒的表达,消除抗性基因。Cre质粒的消除通过挑取单菌落接种到LB液体培养基中,50℃摇床培养12h消除。通过点板无抗、添加氯霉素抗生素、添加卡纳抗生素的LB平板进行筛选,挑选成功消除氯霉素抗性和Cre质粒的单菌落,最后得到分别整合P43-floA和P43-floT的重组枯草芽孢杆菌,命名为BSQ1和BSQ2。
实施例2:重组枯草芽孢杆菌BSQ12的构建
在实施例1得到的BSQ1的基础上采用与实施例1类似的方法,将P43启动子整合在BSQ1基因组上floT的上游,构建重组枯草芽孢杆菌BSQ12。
将实施例1构建好的floTup-lox71-zeo-lox66-p43-floT融合表达框通过化学转化的方式转入BSQ1中,经氯霉素抗性平板筛选、菌落PCR验证、测序、转入Cre质粒、卡纳抗性平板筛选、IPTG诱导表达、Cre质粒消除、点板验证,最后获得整合P43-floA和P43-floT表达框的重组枯草芽孢杆菌BSQ12。
实施例3:菌株发酵生产MK-7
(1)种子液制备
将重组枯草芽孢杆菌BS20、以及实施例1、2中构建的BSQ1、BSQ2、BSQ12挑取单菌落分别接种到15mL摇菌管中,每管含有2mL液体种子培养基,在37℃、220rpm条件下摇床培养10h。BS20作为对照,每株菌三个平行。
(2)发酵培养
将步骤(1)得到的种子液按照10%的接种量接种到250mL锥形瓶中,每瓶装有发酵培养基20mL,于41℃、220rpm条件下摇床培养3d,每隔24h取样进行OD600的检测和样品的制备。具体方法如下。
每天取发酵液1.2mL。取20μL发酵液,用无菌水稀释50倍,摇晃均匀,进行OD600的检测;取500μL发酵液加入到4倍体积的MK-7萃取剂中,涡旋振荡提取10min后,滤出提取液,8000r/min离心5min。收集上清液,HPLC检测全细胞组分MK-7的含量。检测结果见图1。发酵6天后,BSQ1菌株产量达到417.08mg/L,较BS20菌株提升了16.57%;BSQ2菌株在发酵前期MK-7含量略有增加,发酵后期产量明显降低;BSQ12菌株在发酵过程中MK-7含量均低于对照,后期下降幅度增大。结果表明强化FMMs脚手架蛋白合成基因floA、floT对MK-7产量的合成是有影响的,其中floA对MK-7的合成有一定的正向效果,达到了提升MK-7产量的效果。
以上所述实施例仅是为充分说明本发明而所举的较佳的实施例,本发明的保护范围不限于此。本技术领域的技术人员在本发明基础上所作的等同替代或变换,均在本发明的保护范围之内。本发明的保护范围以权利要求书为准。
序列表
<110> 江南大学
<120> 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法
<160> 6
<170> SIPOSequenceListing 1.0
<210> 1
<211> 1000
<212> DNA
<213> (人工序列)
<400> 1
agatcacatt tatatggcgc ctggcggaaa aatgggagcc gccgcgattg ttgatggcca 60
aggcaatgcc gctgaccaaa aagctcaatc actttggctg gcagagatgg aagatgccgc 120
agtgaaaaat aaccgcgatc caaaatatgc gctcgcaatg gctgacccag atatagatgc 180
caaggaagtt ggcgcgccta agggagatct gctgacactt aacgcagaca aggcgattga 240
ggtaggctat tcagaaggca ctgctgacaa tttgtccacg ctcgtaaaga agcttgggtt 300
cgaaaaggcg cagatcagct atgcaaagga gagctttgcg gaaaagacgg caagatggct 360
gacgaatccg gtcattgtcc ctattctgct gacaatcgct tttttaggtc tgacggtaga 420
gcttttttcc ccgggtgtcg gcctccctgg aacggctgga ctcattgcgt tattgctgtt 480
cttttacggg catcttgcag ccggccttgc cgggtatgag acggttctcc tctttatagc 540
aggggtgatt ctcattctgc ttgagatttt tcttcccgga ggaatcattg gattactggg 600
cttgggagcg attattgcga gcctgttttt agccgcgggg agcttcactg tcatggcggt 660
ttctctcttg atcgcctcag ctgtttcgat tacagctttt attttactga caagggtgtt 720
gggaaagcgt atgaaattct ttaagaaatt gatattaaat gattctacaa acacggagag 780
cggctacgtt tcaaatcaaa cgcgcacgga cttaatggga aaagtgggta taacctttac 840
accgctgcgt ccttccggta ccgtgattat tgatgatgaa cgccttgacg ttgtatcgga 900
gggatcgttt acagaaaaag ataaaaaagt aaaagtgata aaagtagaag gctcacgcat 960
tgtcgtgaga gaaatttaaa tagaaacgag gagaagttat 1000
<210> 2
<211> 1309
<212> DNA
<213> (人工序列)
<400> 2
gagcggataa caatttcaca caggaaacag ctatgaccat gattacgaat tcgagctcgg 60
tacccgggga tcctctagag attgtaccgt tcgtatagca tacattatac gaagttatgc 120
catagtgact ggcgatgctg tcggaatgga cgacggcaat agttaccctt attatcaaga 180
taagaaagaa aaggattttt cgctacgctc aaatccttta aaaaaacaca aaagaccaca 240
ttttttaatg tggtctttta ttcttcaact aaagcaccca ttagttcaac aaacgaaaat 300
tggataaagt gggatatttt taaaatatat atttatgtta cagtaatatt gacttttaaa 360
aaaggattga ttctaatgaa gaaagcagac aagtaagcct cctaaattca ctttagataa 420
aaatttagga ggcatatcaa atgaacttta ataaaattga tttagacaat tggaagagaa 480
aagagatatt taatcattat ttgaaccaac aaacgacttt tagtataacc acagaaattg 540
atattagtgt tttataccga aacataaaac aagaaggata taaattttac cctgcattta 600
ttttcttagt gacaagggtg ataaactcaa atacagcttt tagaactggt tacaatagcg 660
acggagagtt aggttattgg gataagttag agccacttta tacaattttt gatggtgtat 720
ctaaaacatt ctctggtatt tggactcctg taaagaatga cttcaaagag ttttatgatt 780
tatacctttc tgatgtagag aaatataatg gttcggggaa attgtttccc aaaacaccta 840
tacctgaaaa tgctttttct ctttctatta ttccatggac ttcatttact gggtttaact 900
taaatatcaa taataatagt aattaccttc tacccattat tacagcagga aaattcatta 960
ataaaggtaa ttcaatatat ttaccgctat ctttacaggt acatcattct gtttgtgatg 1020
gttatcatgc aggattgttt atgaactcta ttcaggaatt gtcagatagg cctaatgact 1080
ggcttttata atatgagata atgccgactg tactttttac agtcggtttt ctaacgatac 1140
attaataggt acgaaaaagc aacttttttt gcgcttaaaa ccagtcatac caataaataa 1200
cttcgtatag catacattat acgaacggta gaatcgtcga cctgcaggca tgcaagcttg 1260
gcactggccg tcgttttaca acgtcgtgac tgggaaaacc ctggcgtta 1309
<210> 3
<211> 300
<212> DNA
<213> (人工序列)
<400> 3
tgataggtgg tatgttttcg cttgaacttt taaatacagc cattgaacat acggttgatt 60
taataactga caaacatcac cctcttgcta aagcggccaa ggacgctgcc gccggggctg 120
tttgcgtttt tgccgtgatt tcgtgtatca ttggtttact tatttttttg ccaaagctgt 180
aatggctgaa aattcttaca tttattttac atttttagaa atgggcgtga aaaaaagcgc 240
gcgattatgt aaaatataaa gtgatagcgg taccattata ggtaagagag gaatgtacac 300
<210> 4
<211> 996
<212> DNA
<213> (人工序列)
<400> 4
atggatccgt caacacttat gattctggca attgtcgcag tagcgatcat tgttttggca 60
gtatttttta catttgtgcc tgtaatgctt tggatttcag ctttggcagc cggagtgaaa 120
atcagcattt tcactctagt tgggatgagg cttcgccgcg tcattccgaa tcgggttgtt 180
aacccgctga ttaaagcgca taaagcggga cttaatgttg gaacaaacca gcttgaaagc 240
cactatctgg ctggaggtaa tgttgacaga gtcgtcaacg cgcttatcgc cgctcagcga 300
gctaacattg aactcacatt cgagcgctgt gctgccattg atcttgcagg ccgggacgtg 360
ttggaagctg ttcaaatgag cgttaatcct aaggtgattg aaacaccgtt cattgccggc 420
gtcgcaatgg acgggattga agtgaaagcg aaagcgagaa tcacagtaag agcgaatatc 480
gagcgcctcg tcgggggagc aggggaagaa accattgtag ctcgtgtagg tgagggaatc 540
gtttctacaa tcggttcatc tgataatcat aaaaaagtgc ttgaaaaccc tgacatgatt 600
tctcagacag tccttggaaa aggattggac tcaggaactg cgtttgaaat tctctcaatt 660
gatattgcag atgtagatat cggcaaaaac atcggggcaa ttttacaaac cgatcaggcc 720
gaggctgata aaaacatcgc gcaggcaaaa gcggaagaac gacgtgcgat ggctgtcgct 780
caagaacagg aaatgcgtgc ccgcgtagaa gaaatgcgcg cgaaagtagt agaagccgag 840
gcggaagtgc cgcttgcgat ggcagaagct ttgcgtgaag ggaatattgg cgtcatggat 900
tacatgaata tcaagaacat cgatgctgac acagaaatgc gtgattcatt cggcaagctg 960
acgaaagacc cttcggatga agaccgcaaa tcataa 996
<210> 5
<211> 1000
<212> DNA
<213> (人工序列)
<400> 5
ttggctgcct gaaataaaat catgcgcagg ctcaagatga ctcggggctt tccgtttatt 60
atttctgtcc tgtgctactt caagcggttt ttcttcaatt tctttaatcg gagcgtcctt 120
tacacgttcc ttcaacattt tttgtgcggt catatcgatt tttttcaaat ggtcaagaac 180
ttcccgtatg ctccattctt cagcagaagg cttttgattc agcttttcgt cagaaagtcc 240
tttcaattcg ttccacgttt ctaatctggc ttcattaaag atactcatca tatctcctcc 300
taaaatgaca ttaccatata tataagcaat tatcatttat aaagcacttc aaatgggtta 360
tttgtcttaa aattttgaaa cttttcccga ggtgtctcgt ataaatggta acggcagccg 420
ttcatcaatg cattgatgaa gaaaggatga ggaagttgga gttatttgga gtacctatac 480
aaacaatgta tctttatacg cttattattg cgggcagcct tacgctgtta ttcctgtttt 540
tcggagatgt attttcaggg ctgtcagaag gcattccgtt tcttaatccg acattagtgc 600
tctcattttt tacatgtttt tcagcgggcg gatatatagg tgaacttgta ttgcctctgt 660
caagcttgct gattgcgctt ttatcttgca tcctttcgat catgctggtg gtattgcttc 720
acatctttgt actggtgcca ttatcatctg cagaagaatc attggcatat agagaagatg 780
atctcagagg aagactcggt aaagtgatta cagctgtgcc ggttgacggg tttggtgaag 840
tggtcataga agggataggc gggaccattt caaagtcagc ggtcagtttt gataatcagc 900
agatcagtta cgggacaacg gtgttagtcg tagatattaa caacggagtt ctttcggtta 960
ctccgcatga acccatttaa cataaaagga ggaatttgat 1000
<210> 6
<211> 1000
<212> DNA
<213> (人工序列)
<400> 6
atgacaatgc cgattataat gatcatcgga gttgtattct ttttattaat tgcactaata 60
gctgtgttta ttacgaagta tcgtacagca gggcctgatg aagcgttaat tgtaacaggg 120
agctatctgg gtaataaaaa tgttcatgtc gatgaaggcg gcaaccgtat taaaatcgtc 180
cgcggcggag gaacctttgt ccttcccgtc ttccagcagg cagagccgct aagcctatta 240
tcaagcaaac tcgatgtttc gacacctgaa gtctatacag aacaaggagt gccagtaatg 300
gccgatggaa ctgcgattat taaaatcggc ggttctatag gagaaatcgc tacagcggcc 360
gaacaatttt tagggaaatc aaaagacgac cgtgagcagg aagcgcggga ggttttagaa 420
ggccaccttc gttccattct cggctcaatg acagtagaag aaatctataa aaacagagaa 480
aaattctctc aagaggtgca gcgtgtcgct tcacaggatc tcgcgaaaat gggacttgta 540
atcgtctcgt ttaccattaa agatgttcgt gataaaaacg gttatcttga atcattaggg 600
aaaccgagaa ttgcccaagt aaaacgcgat gctgatatcg caacagcaga ggctgataaa 660
gaaacccgaa ttaagcgggc agaagccgat aaagacgcaa aaaaatcaga acttgaacgg 720
gcgacggaaa tcgctgaagc tgaaaaaatc aatcagctca aaatggctga attccgcaga 780
gaacaagata cggcaaaagc gaatgccgac caagcatatg atttagagac tgcccgagcg 840
cgccagcaag tcacagagca ggaaatgcag gttaaaatta tcgaacgcca aaaacaaata 900
gaactagaag aaaaagaaat tcttcgccgt gaacgtcaat acgactcaga ggtaaagaaa 960
aaagccgatg cagaccgtta ttctgttgag cagtccgcag 1000
Claims (10)
1.一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法,其特征在于,所述方法是通过强化表达产七烯甲萘醌的枯草芽孢杆菌功能膜微域中的脚手架蛋白FloA。
2.根据权利要求1所述的方法,其特征在于,所述的强化表达是通过使用强启动子进行强化表达。
3.根据权利要求1所述的方法,其特征在于,所述的强启动子为P43启动子。
4.一种产七烯甲萘醌的枯草芽孢杆菌重组菌,其特征在于,所述的枯草芽孢杆菌重组菌是通过强化表达枯草芽孢杆菌宿主功能膜微域中的脚手架蛋白FloA获得。
5.根据权利要求4所述的枯草芽孢杆菌重组菌,其特征在于,所述的强化表达是通过使用强启动子P43进行强化表达。
6.根据权利要求5所述的枯草芽孢杆菌重组菌,其特征在于,所述的强启动子P43的核苷酸序列如SEQ ID NO.3所示。
7.根据权利要求4所述的枯草芽孢杆菌重组菌,其特征在于,所述的枯草芽孢杆菌宿主为枯草芽孢杆菌BS20。
8.根据权利要求4所述的枯草芽孢杆菌重组菌,其特征在于,所述的脚手架蛋白FloA的编码基因的核苷酸序列如SEQ ID NO.4所示。
9.权利要求4~8任一项所述的枯草芽孢杆菌重组菌在发酵生产七烯甲萘醌中的应用。
10.根据权利要求9所述的应用,其特征在于,所述应用具体是将重组枯草芽孢杆菌在种子培养基中活化,然后将活化后的种子转入发酵培养基,进行发酵培养,获得七烯甲萘醌。
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111035771.0A CN113736815B (zh) | 2021-09-06 | 2021-09-06 | 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN202111035771.0A CN113736815B (zh) | 2021-09-06 | 2021-09-06 | 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN113736815A true CN113736815A (zh) | 2021-12-03 |
CN113736815B CN113736815B (zh) | 2022-05-24 |
Family
ID=78735809
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN202111035771.0A Active CN113736815B (zh) | 2021-09-06 | 2021-09-06 | 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN113736815B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115125181A (zh) * | 2022-06-24 | 2022-09-30 | 天津大学青岛海洋技术研究院 | 枯草芽孢杆菌中甲基萘醌-7储存空间的构建方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180076414A (ko) * | 2016-12-27 | 2018-07-06 | 민병규 | 메나퀴논-7 생성능이 향상된 신균주 바실러스 서브틸리스 bsm-k02 및 이를 이용한 메나퀴논-7의 대량 생산 방법 |
CN108998402A (zh) * | 2018-08-28 | 2018-12-14 | 江南大学 | 一种重组枯草芽孢杆菌及其构建方法与应用 |
CN110229841A (zh) * | 2019-06-04 | 2019-09-13 | 江南大学 | 一种增加基因menA拷贝数提高MK-7的产量的方法 |
CN110295135A (zh) * | 2019-07-23 | 2019-10-01 | 江南大学 | 一种改造枯草芽孢杆菌FMMs的方法及其应用 |
-
2021
- 2021-09-06 CN CN202111035771.0A patent/CN113736815B/zh active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20180076414A (ko) * | 2016-12-27 | 2018-07-06 | 민병규 | 메나퀴논-7 생성능이 향상된 신균주 바실러스 서브틸리스 bsm-k02 및 이를 이용한 메나퀴논-7의 대량 생산 방법 |
CN108998402A (zh) * | 2018-08-28 | 2018-12-14 | 江南大学 | 一种重组枯草芽孢杆菌及其构建方法与应用 |
US20200071778A1 (en) * | 2018-08-28 | 2020-03-05 | Jiangnan University | Recombinant bacillus subtilis and use thereof |
CN110229841A (zh) * | 2019-06-04 | 2019-09-13 | 江南大学 | 一种增加基因menA拷贝数提高MK-7的产量的方法 |
CN110295135A (zh) * | 2019-07-23 | 2019-10-01 | 江南大学 | 一种改造枯草芽孢杆菌FMMs的方法及其应用 |
Non-Patent Citations (1)
Title |
---|
JOHANNES SCHNEIDER 等: "Spatio-temporal Remodeling of Functional Membrane Microdomains Organizes the Signaling Networks of a Bacterium", 《PLOS》 * |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115125181A (zh) * | 2022-06-24 | 2022-09-30 | 天津大学青岛海洋技术研究院 | 枯草芽孢杆菌中甲基萘醌-7储存空间的构建方法 |
Also Published As
Publication number | Publication date |
---|---|
CN113736815B (zh) | 2022-05-24 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN110229772B (zh) | 一种提高七稀甲萘醌产量的重组枯草芽孢杆菌及其应用 | |
CN110229841B (zh) | 一种增加基因menA拷贝数提高MK-7的产量的方法 | |
CN111117942B (zh) | 一种产林可霉素的基因工程菌及其构建方法和应用 | |
JP7489134B2 (ja) | D-プシコース3-エピメラーゼ産生菌株及びその使用 | |
CN109777788B (zh) | 一种亮氨酸脱氢酶突变体及其应用 | |
CN114317384B (zh) | 生产2’-岩藻糖基乳糖的重组枯草芽孢杆菌及其构建方法和应用 | |
CN117737149A (zh) | 一种酶催化高效合成高纯度s-玻色因的方法 | |
CN113736815A (zh) | 一种通过强化枯草芽孢杆菌功能膜微域提高七烯甲萘醌产量的方法 | |
CN114672525B (zh) | N-乙酰基-5-甲氧基色胺的生物合成方法及其应用 | |
CN104862326B (zh) | 一种绿僵菌氧甲基转移酶及其应用 | |
CN118813432B (zh) | 用于发酵法生产d-阿洛酮糖的重组菌及其制备方法 | |
CN110029069A (zh) | 一株浅黄霉素基因簇敲除的须糖多孢菌工程菌株及其应用 | |
CN116478894B (zh) | 一种提高唾液酸乳糖产量的基因工程菌及其生产方法 | |
CN112410353A (zh) | 一种fkbS基因、含其的基因工程菌及其制备方法和用途 | |
WO2020075787A1 (ja) | トリコデルマ・リーセイ変異株およびタンパク質の製造方法 | |
CN107287172B (zh) | 一种利用大肠杆菌发酵生产胸苷磷酸化酶的方法 | |
US8137946B2 (en) | Recombinant GRAS strains expressing thermophilic arabinose isomerase as an active form and method of preparing food grade tagatose by using the same | |
US10351857B2 (en) | Marine bacterial gene LfliZ and use | |
CN117586991B (zh) | β-N-乙酰氨基己糖苷酶FlaNag2353及其应用 | |
KR20200093274A (ko) | 최소 유전체를 갖는 신규 미생물 및 이의 제조 방법 | |
CN117603930B (zh) | 一种表达突变型西罗血红素合酶的重组菌 | |
CN119552890B (zh) | 用于提高三角褐指藻中岩藻黄素含量的热激转录因子49557基因及其应用 | |
CN115725535B (zh) | 一种n-脱氧核糖转移酶及其在脱氧核苷制备中的应用 | |
CN118406626B (zh) | 一种小白链霉菌基因工程菌及其应用 | |
CN119709677B (zh) | 一种糖基转移酶及其在制备金线莲苷中的应用 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
EE01 | Entry into force of recordation of patent licensing contract |
Application publication date: 20211203 Assignee: NANTONG LICHENG BIOLOGICAL ENGINEERING Co.,Ltd. Assignor: Jiangnan University Contract record no.: X2025980006526 Denomination of invention: A method for enhancing the production of heptaene naphthoquinone by strengthening the functional membrane microdomain of Bacillus subtilis Granted publication date: 20220524 License type: Common License Record date: 20250401 |
|
EE01 | Entry into force of recordation of patent licensing contract |