Yeeo from Escherichia coli exports flavins

Bioengineered Bugs

Volumn 5, Issue 6, 2014, Pages 386-392

  McAnulty, Michael J ^a   Wood, Thomas K ^a,b  

^a The Pennsylvania State University   (United States)

^b PENNSYLVANIA STATE UNIVERSITY   (United States)

Author keywords

Flavin; Flavin adenine dinucleotide; Flavin mononucleotide; Transporter

Indexed keywords

BACTERIAL PROTEIN; FLAVINE ADENINE NUCLEOTIDE; FLAVINE MONONUCLEOTIDE; MULTIDRUG AND TOXIC COMPOUND EXTRUSION PROTEIN; PROTEIN YEEO; UNCLASSIFIED DRUG; ESCHERICHIA COLI PROTEIN; RIBOFLAVIN DERIVATIVE; BIOFUEL; QUERCETIN; RIBOFLAVIN;

ARTICLE; BACTERIAL GROWTH; BACTERIAL STRAIN; CELL ELONGATION; CELL FUNCTION; CYTOLYSIS; ESCHERICHIA COLI; FLUORESCENCE MICROSCOPY; GENOTYPE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; NONHUMAN; PLASMID; PROTEIN EXPRESSION; PROTEIN SECRETION; METABOLISM; TRANSPORT AT THE CELLULAR LEVEL; CONTROLLED STUDY; SECRETION (PROCESS);

ESCHERICHIA COLI;

BIOLOGICAL TRANSPORT; ESCHERICHIA COLI; ESCHERICHIA COLI PROTEINS; FLAVIN MONONUCLEOTIDE; FLAVIN-ADENINE DINUCLEOTIDE; FLAVINS;

EID: 84922059063     PISSN: 19491018     EISSN: 19491026     Source Type: Journal    
DOI: 10.4161/21655979.2014.969173     Document Type: Article

References (30)

1. Stahmann KP, Revuelta JL, Seulberger H. Three biotechnical processes using Ashbya gossypii, Candida famata, or Bacillus subtilis compete with chemical riboflavin production. Appl Microbiol Biotechnol 2000; 53:509-16. PMID:10855708 http://dx.doi.org/10.1007/s002530051649
2. Grobin A, Hird G, Lambert B, Onai K, Pullen S, inventors; Eisai Co. Ltd., assignee. Pharmaceutical composition comprising 50 monophosphate ester of riboflavin and solubilized riboflavin. United States patent US 20030162751 A1. 2001 Aug 28.
3. Grimmer J, Kiefer H, inventors; BASF Aktiengesellschaft, assignee. Preparation of riboflavin 50-phosphate (fmn) and its sodium salt in a lactone. United States patent US 5095115 A. 1992 March 10.
4. Krauss U, Svensson V, Wirtz A, Knieps-Grunhagen E, Jaeger K-E. Cofactor trapping, a new method to produce flavin mononucleotide. Appl Environ Microbiol 2011; 77:1097-100. PMID:21131527 http://dx.doi.org/10.1128/AEM.01541-10
5. von Canstein H, Ogawa J, Shimizu S, Lloyd JR. Secretion of flavins by Shewanella species and their role in extracellular electron transfer. Appl Environ Microbiol 2008; 74:615-23. PMID:18065612 http://dx.doi.org/10.1128/AEM.01387-07
6. Velasquez-Orta SB, Head IM, Curtis TP, Scott K, Lloyd JR, von Canstein H. The effect of flavin electron shuttles in microbial fuel cells current production. Appl Microbiol Biotechnol 2010; 85:1373-81. PMID:19697021 http://dx.doi.org/10.1007/s00253-009-2172-8
7. Masuda M, Freguia S, Wang Y-F, Tsujimura S, Kano K. Flavins contained in yeast extract are exploited for anodic electron transfer by Lactococcus lactis. Bioelectrochemistry 2010; 78:173-5. PMID:19717350 http://dx.doi.org/10.1016/j.bioelechem.2009.08.004
8. Khan MT, Browne WR, van Dijl JM, Harmsen HJM. How can Faecalibacterium prausnitzii employ riboflavin for extracellular electron transfer? Antioxid Redox Sign 2012; 17:1433-40 http://dx.doi.org/10.1089/ars.2012.4701
9. Mironov VN, Kraev AS, Chikindas ML, Chernov BK, Stepanov AI, Skryabin KG. Functional organization of the riboflavin biosynthesis operon from Bacillus subtilis SHgw. Mol Gen Genet 1994; 242:201-8. PMID: 8159171 http://dx.doi.org/10.1007/BF00391014
10. Perkins JB, Sloma A, Hermann T, Theriault K, Zachgo E, Erdenberger T, Hannett N, Chatterjee NP, Williams V, Rufo GA, et al. Genetic engineering of Bacillus subtilis for the commercial production of riboflavin. J Ind Microbiol Biotechnol 1999; 22:8-18 http://dx.doi.org/10.1038/sj.jim.2900587
11. Humbelin M, Griesser V, Keller T, Schurter W, Haiker M, Hohmann H-P, Ritz H, Richter G, Bacher A, van Loon APGM. GTP cyclohydrolase II and 3,4-dihydroxy-2-butanone 4-phosphate synthase are rate-limiting enzymes in riboflavin synthesis of an industrial Bacillus subtilis strain used for riboflavin production. J Ind Microbiol Biotechnol 1999; 22:1-7 http://dx.doi.org/10.1038/sj.jim.2900590
12. Yatsyshyn VY, Ishchuk OP, Voronovsky AY, Fedorovych DV, Sibirny AA. Production of flavin mononucleotide by metabolically engineered yeast Candida famata. Metab Eng 2009; 11:163-7. PMID:19558965 http://dx.doi.org/10.1016/j.ymben.2009.01.004
13. Hemberger S, Pedrolli DB, Stolz J, Vogl C, Lehmann M, Mack M. RibM from Streptomyces davawensis is a riboflavin/roseoflavin transporter and may be useful for the optimization of riboflavin production strains. BMC Biotechnol 2011; 11:119. PMID:22136195
14. Rabinovich PM, Beburov M Iu, Linevich ZK, Bandrin SV, Stepanov AI. Expression of Bacillus subtilis riboflavin operon in Escherichia coli cells in the form of hybrid plasmids pPR1 and pPR2. Dokl Akad Nauk SSSR 1978; 238:1459-61. PMID:415855
15. Kotloski NJ, Gralnick JA. Flavin electron shuttles dominate extracellular electron transfer by Shewanella oneidensis. MBio 2013; 4:pii: e00553-12. PMID:23322638 http://dx.doi.org/10.1128/mBio.00553-12
16. Abbas CA, Sibirny AA. Genetic control of biosynthesis and transport of riboflavin and flavin nucleotides and construction of robust biotechnological producers. Microbiol Mol Biol Rev 2011; 75:321-60. PMID: 21646432 http://dx.doi.org/10.1128/MMBR.00030-10
17. Worst DJ, Gerrits MM, Vandenbroucke-Grauls CM JE, Kusters JG. Helicobacter pylori ribBA-mediated riboflavin production is involved in iron acquisition. J Bacteriol 1998; 180:1473-9. PMID:9515916
18. Moriyama Y, Hiasa M, Matsumoto T, Omote H. Multidrug and toxic compound extrusion (MATE)-type proteins as anchor transporters for the excretion of metabolic waste products and xenobiotics. Xenobiotica 2008; 38:1107-18. PMID:18668441 http://dx.doi.org/10.1080/00498250701883753
19. Hayashi M, Tabata K, Yagasaki M, Yonetani Y. Effect of multidrug-efflux transporter genes on dipeptide resistance and overproduction in Escherichia coli. FEMSMicrobiol Lett 2010; 304:12-9. PMID:20067529 http://dx.doi.org/10.1111/j.1574-6968.2009.01879.x
20. Nichols RJ, Sen S, Choo YJ, Beltrao P, Zietek M, Chaba R, Lee S, Kazmierczak KM, Lee KJ, Wong A, et al. Phenotypic landscape of a bacterial cell. Cell 2011; 144:143-56. PMID:21185072 http://dx.doi.org/10.1016/j.cell.2010.11.052
21. Wilson AC, Pardee AB. Regulation of flavin synthesis by Escherichia coli. J Gen Microbiol 1962; 28:283-303. PMID:14007303 http://dx.doi.org/10.1099/00221287-28-2-283
22. Covington ED, Gelbmann CB, Kotloski NJ, Gralnick JA. An essential role for UshA in processing of extracellular flavin electron shuttles by Shewanella oneidensis. Mol Microbiol 2010; 78:519-32. PMID:20807196 http://dx.doi.org/10.1111/j.1365-2958.2010.07353.x
23. Baba T, Ara T, Hasegawa M, Takai Y, Okumura Y, Baba M, Datsenko KA, Tomita M, Wanner BL, Mori H. Construction of Escherichia coli K-12 in-frame, single-gene knockout mutants: the Keio collection. Mol Syst Biol 2006; 2:2006-0008. PMID:16738554 http://dx.doi.org/10.1038/msb4100050
24. Kitagawa M, Ara T, Arifuzzaman M, Ioka-Nakamichi T, Inamoto E, Toyonaga H, Mori H. Complete set of ORF clones of Escherichia coli ASKA library (a complete set of E. coli K-12 ORF archive): unique resources for biological research. DNA Res 2005; 12:291-9. PMID:16769691 http://dx.doi.org/10.1093/dnares/dsi012
25. Sambrook JFE, Maniatis T. Molecular Cloning: a Laboratory Manual. Cold Spring Harbor, N.Y.: Cold Spring Harbor Laboratory Press, 1989.
26. Rodriguez RL, Tait RC. Recombinant DNA techniques: an introduction. Menlo Park, Calif.: The Benjamin /Cummings Publishing Company, Inc., 1983.
27. Vardar G, Wood TK. Protein engineering of toluene-oxylene monooxygenase from Pseudomonas stutzeri OX1 for synthesizing 4-methylresorcinol, methylhydroquinone, and pyrogallol. Appl Environ Microbiol 2004; 70:3253-62. PMID:15184119 http://dx.doi.org/10.1128/AEM.70.6.3253-3262.2004
28. Volkmer B, Heinemann M. Condition-dependent cell volume and concentration of Escherichia coli to facilitate data conversion for systems biology modeling. PloS One 2011; 6:e23126. PMID:21829590 http://dx.doi.org/10.1371/journal.pone.0023126
29. Pallotta ML. Evidence for the presence of a FAD pyrophosphatase and a FMN phosphohydrolase in yeast mitochondria: a possible role in flavin homeostasis. Yeast 2011; 28:693-705. PMID:21915900 http://dx.doi.org/10.1002/yea.1897
30. Soo VWC, Hanson-Manful P, Patrick WM. Artificial gene amplification reveals an abundance of promiscuous resistance determinants in Escherichia coli. ProcNatl Acad Sci U S A 2011; 108:1484-9. PMID:21173244 http://dx.doi.org/10.1073/pnas.1012108108