This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
Ali Z, Wang Z, Amir RM, Younas S, Wali A, Adowa N, Ayim I. Potential uses of vinegar as a medicine and related in vivo mechanisms. Int J Vitam Nutr Res. 2016 Jun;86(3–4):127–151. https://doi.org/10.1024/0300-9831/a000440AliZWangZAmirRMYounasSWaliAAdowaNAyimI. Potential uses of vinegar as a medicine and related in vivo mechanisms. . 2016Jun;86(3–4):127–151. https://doi.org/10.1024/0300-9831/a00044010.1024/0300-9831/a000440Search in Google Scholar
Anders S, Huber W. Differential expression analysis for sequence count data. Genome Biol. 2010 Oct;11(10):R106. https://doi.org/10.1186/gb-2010-11-10-r106AndersSHuberW. Differential expression analysis for sequence count data. . 2010Oct;11(10):R106. https://doi.org/10.1186/gb-2010-11-10-r10610.1186/gb-2010-11-10-r106Search in Google Scholar
Andrés-Barrao C, Saad MM, Chappuis ML, Boffa M, Perret X, Ortega Pérez R, Barja F. Proteome analysis of Acetobacter pasteurianus during acetic acid fermentation. J Proteomics. 2012 Mar; 75(6):1701–1717. https://doi.org/10.1016/j.jprot.2011.11.027Andrés-BarraoCSaadMMChappuisMLBoffaMPerretXOrtega PérezRBarjaF. Proteome analysis of Acetobacter pasteurianus during acetic acid fermentation. . 2012Mar; 75(6):1701–1717. https://doi.org/10.1016/j.jprot.2011.11.02710.1016/j.jprot.2011.11.027Search in Google Scholar
Benjak A, Uplekar S, Zhang M, Piton J, Cole ST, Sala C. Genomic and transcriptomic analysis of the streptomycin-dependent Mycobacterium tuberculosis strain 18b. BMC Genomics. 2016 Dec; 17(1):190. https://doi.org/10.1186/s12864-016-2528-2BenjakAUplekarSZhangMPitonJColeSTSalaC. Genomic and transcriptomic analysis of the streptomycin-dependent Mycobacterium tuberculosis strain 18b. . 2016Dec; 17(1):190. https://doi.org/10.1186/s12864-016-2528-210.1186/s12864-016-2528-2Search in Google Scholar
Chen Y, Bai Y, Li D, Wang C, Xu N, Hu Y. Screening and characterization of ethanol-tolerant and thermotolerant acetic acid bacteria from Chinese vinegar Pei. World J Microbiol Biotechnol. 2016 Jan;32(1):14. https://doi.org/10.1007/s11274-015-1961-8ChenYBaiYLiDWangCXuNHuY. Screening and characterization of ethanol-tolerant and thermotolerant acetic acid bacteria from Chinese vinegar Pei. . 2016Jan;32(1):14. https://doi.org/10.1007/s11274-015-1961-810.1007/s11274-015-1961-8Search in Google Scholar
Chinnawirotpisan P, Theeragool G, Limtong S, Toyama H, Adachi OO, Matsushita K. Quinoprotein alcohol dehydrogenase is involved in catabolic acetate production, while NAD-dependent alcohol dehydrogenase in ethanol assimilation in Acetobacter pasteurianus SKU1108. J Biosci Bioeng. 2003 Jan;96(6):564–571. https://doi.org/10.1016/S1389-1723(04)70150-4ChinnawirotpisanPTheeragoolGLimtongSToyamaHAdachiOOMatsushitaK. Quinoprotein alcohol dehydrogenase is involved in catabolic acetate production, while NAD-dependent alcohol dehydrogenase in ethanol assimilation in Acetobacter pasteurianus SKU1108. . 2003Jan;96(6):564–571. https://doi.org/10.1016/S1389-1723(04)70150-410.1016/S1389-1723(04)70150-4Search in Google Scholar
Clauss-Lendzian E, Vaishampayan A, de Jong A, Landau U, Meyer C, Kok J, Grohmann E. Stress response of a clinical Enterococcus faecalis isolate subjected to a novel antimicrobial surface coating. Microbiol Res. 2018 Mar;207:53–64. https://doi.org/10.1016/j.micres.2017.11.006Clauss-LendzianEVaishampayanAde JongALandauUMeyerCKokJGrohmannE. Stress response of a clinical Enterococcus faecalis isolate subjected to a novel antimicrobial surface coating. . 2018Mar;207:53–64. https://doi.org/10.1016/j.micres.2017.11.00610.1016/j.micres.2017.11.006Search in Google Scholar
Confer AW, Ayalew S. The OmpA family of proteins: roles in bacterial pathogenesis and immunity. Vet Microbiol. 2013 May;163 (3–4):207–222. https://doi.org/10.1016/j.vetmic.2012.08.019ConferAWAyalewS. The OmpA family of proteins: roles in bacterial pathogenesis and immunity. . 2013May;163 (3–4):207–222. https://doi.org/10.1016/j.vetmic.2012.08.01910.1016/j.vetmic.2012.08.019Search in Google Scholar
Filiatrault MJ. Progress in prokaryotic transcriptomics. Curr Opin Microbiol. 2011 Oct;14(5):579–586. https://doi.org/10.1016/j.mib.2011.07.023FiliatraultMJ. Progress in prokaryotic transcriptomics. . 2011Oct;14(5):579–586. https://doi.org/10.1016/j.mib.2011.07.02310.1016/j.mib.2011.07.023Search in Google Scholar
Fukaya M, Takemura H, Tayama K, Okumura H, Kawamura Y, Horinouchi S, Beppu T. The aarC gene responsible for acetic acid assimilation confers acetic acid resistance on Acetobacter aceti. J Ferment Bioeng. 1993 Jan;76(4):270–275. https://doi.org/10.1016/0922-338X(93)90192-BFukayaMTakemuraHTayamaKOkumuraHKawamuraYHorinouchiSBeppuT. The aarC gene responsible for acetic acid assimilation confers acetic acid resistance on Acetobacter aceti. . 1993Jan;76(4):270–275. https://doi.org/10.1016/0922-338X(93)90192-B10.1016/0922-338X(93)90192-BSearch in Google Scholar
Ganguly B, Tewari K, Singh R. Homology modeling, functional annotation and comparative genomics of outer membrane protein H of Pasteurella multocida. J Theor Biol. 2015 Dec;386:18–24. https://doi.org/10.1016/j.jtbi.2015.08.028GangulyBTewariKSinghR. Homology modeling, functional annotation and comparative genomics of outer membrane protein H of Pasteurella multocida. . 2015Dec;386:18–24. https://doi.org/10.1016/j.jtbi.2015.08.02810.1016/j.jtbi.2015.08.02826362105Search in Google Scholar
Gil F, Hernández-Lucas I, Polanco R, Pacheco N, Collao B, Villarreal JM, Nardocci G, Calva E, Saavedra CP. SoxS regulates the expression of the Salmonella enterica serovar Typhimurium ompW gene. Microbiology. 2009 Aug 01;155(8):2490–2497. https://doi.org/10.1099/mic.0.027433-0GilFHernández-LucasIPolancoRPachecoNCollaoBVillarrealJMNardocciGCalvaESaavedraCP. SoxS regulates the expression of the Salmonella enterica serovar Typhimurium ompW gene. . 2009Aug01;155(8):2490–2497. https://doi.org/10.1099/mic.0.027433-010.1099/mic.0.027433-019460824Search in Google Scholar
Gomes RJ, Borges MF, Rosa MF, Castro-Gómez RJH, Spinosa WA. Acetic acid bacteria in the food industry: systematics, characteristics and applications. Food Technol Biotechnol. 2018;56(2):139–151. https://doi.org/10.17113/ftb.56.02.18.5593GomesRJBorgesMFRosaMFCastro-GómezRJHSpinosaWA. Acetic acid bacteria in the food industry: systematics, characteristics and applications. . 2018;56(2):139–151. https://doi.org/10.17113/ftb.56.02.18.559310.17113/ftb.56.02.18.5593611799030228790Search in Google Scholar
Goto H, Masuko M, Ohnishi M, Tsukamoto Y. [Comparative analysis of phospholipids for two Acetobacters producing acetic acid at high and moderate concentrations] (in Japanese). J Jpn Oil Chem Soc. 2000;49:349–355, 390. https://doi.org/10.5650/jos1996.49.349GotoHMasukoMOhnishiMTsukamotoY. [Comparative analysis of phospholipids for two Acetobacters producing acetic acid at high and moderate concentrations] (in Japanese). . 2000;49:349–355, 390. https://doi.org/10.5650/jos1996.49.34910.5650/jos1996.49.349Search in Google Scholar
Gullo M, Verzelloni E, Canonico M. Aerobic submerged fermentation by acetic acid bacteria for vinegar production: process and biotechnological aspects. Process Biochem. 2014 Oct;49(10):1571–1579. https://doi.org/10.1016/j.procbio.2014.07.003GulloMVerzelloniECanonicoM. Aerobic submerged fermentation by acetic acid bacteria for vinegar production: process and biotechnological aspects. . 2014Oct;49(10):1571–1579. https://doi.org/10.1016/j.procbio.2014.07.00310.1016/j.procbio.2014.07.003Search in Google Scholar
Hemmingsen SM, Woolford C, van der Vies SM, Tilly K, Dennis DT, Georgopoulos CP, Hendrix RW, Ellis RJ. Homologous plant and bacterial proteins chaperone oligomeric protein assembly. Nature. 1988 May;333(6171):330–334. https://doi.org/10.1038/333330a0HemmingsenSMWoolfordCvan der ViesSMTillyKDennisDTGeorgopoulosCPHendrixRWEllisRJ. Homologous plant and bacterial proteins chaperone oligomeric protein assembly. . 1988May;333(6171):330–334. https://doi.org/10.1038/333330a010.1038/333330a02897629Search in Google Scholar
Higashide T, Okumura H, Kawamura Y, Teranishi K, Hisamatsu M, Yamada T. [Membrane components and cell form of Acetobactor polyoxogenes (vinegar producing strain) under high acidic conditions] (in Japanese). Nippon Shokuhin Kagaku Kogaku Kaishi. 1996;43(2):117–123. https://doi.org/10.3136/nskkk.43.117HigashideTOkumuraHKawamuraYTeranishiKHisamatsuMYamadaT. [Membrane components and cell form of Acetobactor polyoxogenes (vinegar producing strain) under high acidic conditions] (in Japanese). . 1996;43(2):117–123. https://doi.org/10.3136/nskkk.43.11710.3136/nskkk.43.117Search in Google Scholar
Hong H, Patel DR, Tamm LK, van den Berg B. The outer membrane protein OmpW forms an eight-stranded β-barrel with a hydrophobic channel. J Biol Chem. 2006 Mar;281(11):7568–7577. https://doi.org/10.1074/jbc.M512365200HongHPatelDRTammLKvan den BergB. The outer membrane protein OmpW forms an eight-stranded β-barrel with a hydrophobic channel. . 2006Mar;281(11):7568–7577. https://doi.org/10.1074/jbc.M51236520010.1074/jbc.M51236520016414958Search in Google Scholar
Kondo K, Beppu T, Horinouchi S. Cloning, sequencing, and characterization of the gene encoding the smallest subunit of the three-component membrane-bound alcohol dehydrogenase from Acetobacter pasteurianus. J Bacteriol. 1995 Sep;177(17):5048–5055. https://doi.org/10.1128/jb.177.17.5048-5055.1995KondoKBeppuTHorinouchiS. Cloning, sequencing, and characterization of the gene encoding the smallest subunit of the three-component membrane-bound alcohol dehydrogenase from Acetobacter pasteurianus. . 1995Sep;177(17):5048–5055. https://doi.org/10.1128/jb.177.17.5048-5055.199510.1128/jb.177.17.5048-5055.19951772837665483Search in Google Scholar
Matsushita K, Toyama H, Adachi O. Chapter 4: Respiratory chains in acetic acid bacteria: membranebound periplasmic sugar and alcohol respirations. In: Zannoni D, editor. Respiration in Archaea and Bacteria. Advances in photosynthesis and respiration, vol. 16. Dordrecht (The Netherlands): Springer; 2004. p. 81–99. https://doi.org/10.1007/978-1-4020-3163-2_4MatsushitaKToyamaHAdachiO. Chapter 4: Respiratory chains in acetic acid bacteria: membranebound periplasmic sugar and alcohol respirations. In: ZannoniD, editor. . Dordrecht (The Netherlands): Springer; 2004. p. 81–99. https://doi.org/10.1007/978-1-4020-3163-2_410.1007/978-1-4020-3163-2_4Search in Google Scholar
Mullins EA, Francois JA, Kappock TJ. A specialized citric acid cycle requiring succinyl-coenzyme A (CoA):acetate CoA-transferase (AarC) confers acetic acid resistance on the acidophile Acetobacter aceti. J Bacteriol. 2008 Jul 15;190(14):4933–4940. https://doi.org/10.1128/JB.00405-08MullinsEAFrancoisJAKappockTJ. A specialized citric acid cycle requiring succinyl-coenzyme A (CoA):acetate CoA-transferase (AarC) confers acetic acid resistance on the acidophile Acetobacter aceti. . 2008Jul15;190(14):4933–4940. https://doi.org/10.1128/JB.00405-0810.1128/JB.00405-08Search in Google Scholar
Nakano S, Fukaya M, Horinouchi S. Enhanced expression of aconitase raises acetic acid resistance in Acetobacter aceti. FEMS Microbiol Lett. 2004 Jun;235(2):315–322. https://doi.org/10.1111/j.1574-6968.2004.tb09605.xNakanoSFukayaMHorinouchiS. Enhanced expression of aconitase raises acetic acid resistance in Acetobacter aceti. . 2004Jun;235(2):315–322. https://doi.org/10.1111/j.1574-6968.2004.tb09605.x10.1111/j.1574-6968.2004.tb09605.xSearch in Google Scholar
Nguyen VD, Wolf C, Mäder U, Lalk M, Langer P, Lindequist U, Hecker M, Antelmann H. Transcriptome and proteome analyses in response to 2-methylhydroquinone and 6-brom-2-vinyl-chroman-4-on reveal different degradation systems involved in the catabolism of aromatic compounds in Bacillus subtilis. Proteomics. 2007 May;7(9):1391–1408. https://doi.org/10.1002/pmic.200700008NguyenVDWolfCMäderULalkMLangerPLindequistUHeckerMAntelmannH. Transcriptome and proteome analyses in response to 2-methylhydroquinone and 6-brom-2-vinyl-chroman-4-on reveal different degradation systems involved in the catabolism of aromatic compounds in Bacillus subtilis. . 2007May;7(9):1391–1408. https://doi.org/10.1002/pmic.20070000810.1002/pmic.200700008Search in Google Scholar
Okamoto-Kainuma A, Ishikawa M, Nakamura H, Fukazawa S, Tanaka N, Yamagami K, Koizumi Y. Characterization of rpoH in Acetobacter pasteurianus NBRC3283. J Biosci Bioeng. 2011 Apr;111(4):429–432. https://doi.org/10.1016/j.jbiosc.2010.12.016Okamoto-KainumaAIshikawaMNakamuraHFukazawaSTanakaNYamagamiKKoizumiY. Characterization of rpoH in Acetobacter pasteurianus NBRC3283. . 2011Apr;111(4):429–432. https://doi.org/10.1016/j.jbiosc.2010.12.01610.1016/j.jbiosc.2010.12.016Search in Google Scholar
Okamoto-Kainuma A, Yan W, Kadono S, Tayama K, Koizumi Y, Yanagida F. Cloning and characterization of groESL operon in Acetobacter aceti. J Biosci Bioeng. 2002;94(2):140–147. https://doi.org/10.1016/S1389-1723(02)80134-7Okamoto-KainumaAYanWKadonoSTayamaKKoizumiYYanagidaF. Cloning and characterization of groESL operon in Acetobacter aceti. . 2002;94(2):140–147. https://doi.org/10.1016/S1389-1723(02)80134-710.1016/S1389-1723(02)80134-7Search in Google Scholar
Qi Z, Yang H, Xia X, Quan W, Wang W, Yu X. Achieving high strength vinegar fermentation via regulating cellular growth status and aeration strategy. Process Biochem. 2014 Jul;49(7):1063–1070. https://doi.org/10.1016/j.procbio.2014.03.018QiZYangHXiaXQuanWWangWYuX. Achieving high strength vinegar fermentation via regulating cellular growth status and aeration strategy. . 2014Jul;49(7):1063–1070. https://doi.org/10.1016/j.procbio.2014.03.01810.1016/j.procbio.2014.03.018Search in Google Scholar
Qiu X, Zhang Y, Hong H. Classification of acetic acid bacteria and their acid resistant mechanism. AMB Express. 2021 Dec;11(1):29. https://doi.org/10.1186/s13568-021-01189-6QiuXZhangYHongH. Classification of acetic acid bacteria and their acid resistant mechanism. . 2021Dec;11(1):29. https://doi.org/10.1186/s13568-021-01189-610.1186/s13568-021-01189-6788978233595734Search in Google Scholar
Ryngajłło M, Jacek P, Cielecka I, Kalinowska H, Bielecki S. Effect of ethanol supplementation on the transcriptional landscape of bionanocellulose producer Komagataeibacter xylinus E25. Appl Microbiol Biotechnol. 2019 Aug;103(16):6673–6688. https://doi.org/10.1007/s00253-019-09904-xRyngajłłoMJacekPCieleckaIKalinowskaHBieleckiS. Effect of ethanol supplementation on the transcriptional landscape of bionanocellulose producer Komagataeibacter xylinus E25. . 2019Aug;103(16):6673–6688. https://doi.org/10.1007/s00253-019-09904-x10.1007/s00253-019-09904-x666768231168651Search in Google Scholar
Sakurai K, Arai H, Ishii M, Igarashi Y. Transcriptome response to different carbon sources in Acetobacter aceti. Microbiology. 2011 Mar 01;157(3):899–910. https://doi.org/10.1099/mic.0.045906-0SakuraiKAraiHIshiiMIgarashiY. Transcriptome response to different carbon sources in Acetobacter aceti. . 2011Mar01;157(3):899–910. https://doi.org/10.1099/mic.0.045906-010.1099/mic.0.045906-021081762Search in Google Scholar
Samad A, Azlan A, Ismail A. Therapeutic effects of vinegar: a review. Curr Opin Food Sci. 2016 Apr;8:56–61. https://doi.org/10.1016/j.cofs.2016.03.001SamadAAzlanAIsmailA. Therapeutic effects of vinegar: a review. . 2016Apr;8:56–61. https://doi.org/10.1016/j.cofs.2016.03.00110.1016/j.cofs.2016.03.001Search in Google Scholar
Tesfaye W, Morales ML, García-Parrilla MC, Troncoso AM. Wine vinegar: technology, authenticity and quality evaluation. Trends Food Sci Technol. 2002 Jan;13(1):12–21. https://doi.org/10.1016/S0924-2244(02)00023-7TesfayeWMoralesMLGarcía-ParrillaMCTroncosoAM. Wine vinegar: technology, authenticity and quality evaluation. . 2002Jan;13(1):12–21. https://doi.org/10.1016/S0924-2244(02)00023-710.1016/S0924-2244(02)00023-7Search in Google Scholar
Tjaden B. De novo assembly of bacterial transcriptomes from RNA-seq data. Genome Biol. 2015 Dec;16(1):1. https://doi.org/10.1186/s13059-014-0572-2TjadenB. De novo assembly of bacterial transcriptomes from RNA-seq data. . 2015Dec;16(1):1. https://doi.org/10.1186/s13059-014-0572-210.1186/s13059-014-0572-2431679925583448Search in Google Scholar
Toyama H, Mathews FS, Adachi O, Matsushita K. Quinohemoprotein alcohol dehydrogenases: structure, function, and physiology. Arch Biochem Biophys. 2004 Aug;428(1):10–21. https://doi.org/10.1016/j.abb.2004.03.037ToyamaHMathewsFSAdachiOMatsushitaK. Quinohemoprotein alcohol dehydrogenases: structure, function, and physiology. . 2004Aug;428(1):10–21. https://doi.org/10.1016/j.abb.2004.03.03710.1016/j.abb.2004.03.03715234265Search in Google Scholar
Trapnell C, Williams BA, Pertea G, Mortazavi A, Kwan G, van Baren MJ, Salzberg SL, Wold BJ, Pachter L. Transcript assembly and abundance estimation from RNA-Seq reveals thousands of new transcripts and switching among isoforms. Nat Biotechnol. 2010;28(5):511–515. https://doi.org/10.1038/nbt.1621TrapnellCWilliamsBAPerteaGMortazaviAKwanGvan BarenMJSalzbergSLWoldBJPachterL. Transcript assembly and abundance estimation from RNA-Seq reveals thousands of new transcripts and switching among isoforms. . 2010;28(5):511–515. https://doi.org/10.1038/nbt.162110.1038/nbt.1621314604320436464Search in Google Scholar
Trček J, Mira NP, Jarboe LR. Adaptation and tolerance of bacteria against acetic acid. Appl Microbiol Biotechnol. 2015 Aug;99(15):6215–6229. https://doi.org/10.1007/s00253-015-6762-3TrčekJMiraNPJarboeLR. Adaptation and tolerance of bacteria against acetic acid. . 2015Aug;99(15):6215–6229. https://doi.org/10.1007/s00253-015-6762-310.1007/s00253-015-6762-326142387Search in Google Scholar
Trcek J, Toyama H, Czuba J, Misiewicz A, Matsushita K. Correlation between acetic acid resistance and characteristics of PQQ-dependent ADH in acetic acid bacteria. Appl Microbiol Biotechnol. 2006 Apr;70(3):366–373. https://doi.org/10.1007/s00253-005-0073-zTrcekJToyamaHCzubaJMisiewiczAMatsushitaK. Correlation between acetic acid resistance and characteristics of PQQ-dependent ADH in acetic acid bacteria. . 2006Apr;70(3):366–373. https://doi.org/10.1007/s00253-005-0073-z10.1007/s00253-005-0073-z16133326Search in Google Scholar
Wang B, Shao Y, Chen F. Overview on mechanisms of acetic acid resistance in acetic acid bacteria. World J Microbiol Biotechnol. 2015 Feb;31(2):255–263. https://doi.org/10.1007/s11274-015-1799-0WangBShaoYChenF. Overview on mechanisms of acetic acid resistance in acetic acid bacteria. . 2015Feb;31(2):255–263. https://doi.org/10.1007/s11274-015-1799-010.1007/s11274-015-1799-025575804Search in Google Scholar
Wu X, Yao H, Cao L, Zheng Z, Chen X, Zhang M, Wei Z, Cheng J, Jiang S, Pan L, et al. Improving acetic acid production by Over-Expressing PQQ-ADH in Acetobacter pasteurianus. Front Microbiol. 2017 Sep 06;8:1713. https://doi.org/10.3389/fmicb.2017.01713WuXYaoHCaoLZhengZChenXZhangMWeiZChengJJiangSPanL. Improving acetic acid production by Over-Expressing PQQ-ADH in Acetobacter pasteurianus. . 2017Sep06;8:1713. https://doi.org/10.3389/fmicb.2017.0171310.3389/fmicb.2017.01713559221428932219Search in Google Scholar
Xia K, Zang N, Zhang J, Zhang H, Li Y, Liu Y, Feng W, Liang X. New insights into the mechanisms of acetic acid resistance in Acetobacter pasteurianus using iTRAQ-dependent quantitative proteomic analysis. Int J Food Microbiol. 2016 Dec;238:241–251. https://doi.org/10.1016/j.ijfoodmicro.2016.09.016XiaKZangNZhangJZhangHLiYLiuYFengWLiangX. New insights into the mechanisms of acetic acid resistance in Acetobacter pasteurianus using iTRAQ-dependent quantitative proteomic analysis. . 2016Dec;238:241–251. https://doi.org/10.1016/j.ijfoodmicro.2016.09.01610.1016/j.ijfoodmicro.2016.09.01627681379Search in Google Scholar
Yamada Y, Yukphan P, Vu HTL, Muramatsu Y, Ochaikul D, Nakagawa Y. Subdivision of the genus Gluconacetobacter Yamada, Hoshino and Ishikawa 1998: the proposal of Komagatabacter gen. nov., for strains accommodated to the Gluconacetobacter xylinus group in the α-Proteobacteria. Ann Microbiol. 2012 Jun;62(2):849–859. https://doi.org/10.1007/s13213-011-0288-4YamadaYYukphanPVuHTLMuramatsuYOchaikulDNakagawaY. Subdivision of the genus Gluconacetobacter Yamada, Hoshino and Ishikawa 1998: the proposal of Komagatabacter gen. nov., for strains accommodated to the Gluconacetobacter xylinus group in the α-Proteobacteria. . 2012Jun;62(2):849–859. https://doi.org/10.1007/s13213-011-0288-410.1007/s13213-011-0288-4Search in Google Scholar
Yang H, Yu Y, Fu C, Chen F. Bacterial acid resistance toward organic weak acid revealed by RNA-Seq transcriptomic analysis in Acetobacter pasteurianus. Front Microbiol. 2019 Aug 6;10:1616. https://doi.org/10.3389/fmicb.2019.01616YangHYuYFuCChenF. Bacterial acid resistance toward organic weak acid revealed by RNA-Seq transcriptomic analysis in Acetobacter pasteurianus. . 2019Aug6;10:1616. https://doi.org/10.3389/fmicb.2019.0161610.3389/fmicb.2019.01616669105131447789Search in Google Scholar
Young MD, Wakefield MJ, Smyth GK, Oshlack A. Gene ontology analysis for RNA-seq: accounting for selection bias. Genome Biol. 2010;11(2):R14. https://doi.org/10.1186/gb-2010-11-2-r14YoungMDWakefieldMJSmythGKOshlackA. Gene ontology analysis for RNA-seq: accounting for selection bias. . 2010;11(2):R14. https://doi.org/10.1186/gb-2010-11-2-r1410.1186/gb-2010-11-2-r14287287420132535Search in Google Scholar
Zhai L, Xue Y, Song Y, Xian M, Yin L, Zhong N, Xia G, Ma Y. Overexpression of AaPal, a peptidoglycan-associated lipoprotein from Alkalomonas amylolytica, improves salt and alkaline tolerance of Escherichia coli and Arabidopsis thaliana. Biotechnol Lett. 2014 Mar;36(3):601–607. https://doi.org/10.1007/s10529-013-1398-9ZhaiLXueYSongYXianMYinLZhongNXiaGMaY. Overexpression of AaPal, a peptidoglycan-associated lipoprotein from Alkalomonas amylolytica, improves salt and alkaline tolerance of Escherichia coli and Arabidopsis thaliana. . 2014Mar;36(3):601–607. https://doi.org/10.1007/s10529-013-1398-910.1007/s10529-013-1398-924249101Search in Google Scholar