Abstract
A bacterium that secretes maltooligosaccharide-forming amylase in a medium containing 12.5% (vol/vol) dimethylsulfoxide (DMSO) was isolated and identified as Brachybacterium sp. strain LB25. The amylase of the strain was purified from the culture supernatant, and its molecular mass was 60 kDa. The enzyme was stable at pH 7.0–8.5 and active at pH 6.0–7.5. The optimum temperature at pH 7.0 was 35°C in the presence of 5 mM CaCl2. The enzyme hydrolyzed starch to produce maltotriose primarily. The enzyme was active in the presence of various organic solvents. Its yield and product selectivity of maltooligosaccharides in the presence of DMSO or ethanol were compared with those of the industrial maltotriose-forming amylase from Microbacterium imperiale. Both enzymes improved the production selectivity of maltotriose by the addition of DMSO or ethanol. However, the total maltooligosaccharide yield in the presence of the solvents was higher for LB25 amylase than for M. imperiale amylase.




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Ali M, Mhiri S, Mezghani M, Bejar S (2001) Purification and sequence analysis of the atypical maltohexaose-forming α-amylase of the B. stearothermophilus US100. Enzyme Microb Technol 28:537–542
Antonini E, Carrea G, Cremonesi P (1981) Enzyme catalyzed reactions in water-organic solvent two-phase system. Enzyme Microb Technol 3:291–296
Blackwood A, Bucke C (2000) Addition of polar organic solvents can improve the product selectivity of cyclodextrin glycosyltransferase solvent effects on CGTase. Enzyme Microb Technol 27:704–708
Bradford M (1976) A rapid and sensitive method for the quantitation of microgram quantities of utilizing the principle of protein-dye binding. Anal Biochem 72:248–254
Carrea G (1984) Biocatalysis in water-organic solvent two phase systems. Trends Biotechnol 2:102–106
Doukyu N, Aono R (2001) Cloning, sequence analysis and expression of a gene encoding an organic solvent- and detergent-tolerant cholesterol oxidase of Burkholdria cepacia strain ST-200. Appl Microbiol Biotechnol 57:146–152
Doukyu N, Kuwahara H, Aono R (2003) Isolation of Paenibacillus illinoisensis that produces cyclodextrin glucanotransferase resistant to organic solvents. Biosci Biotechnol Biochem 67:334–340
Fukushima T, Mizuki T, Echigo A, Inoue A, Usami R (2005) Organic solvent tolerance of halophilic α-amylase from a Haloarchaeon, Haloarcula sp. strain S-1. Extremophile 9:85–89
Heyrman J, Balcaen A, Vos P, Schumann P, Swings J (2002) Brachybacterium fresconis sp. nov. and Brachybacterium sacelli sp. nov., isolated from deteriorated parts of a medieval wall painting of the chapel of Castle Herberstein (Austria). Int J Syst Evol Microbiol 52:1641–1646
Kainuma K, Wako K, Kobayashi S, Nogami A, Suzuki S (1975) Purification and some properties from Aerobacter aerogenes. Biochim Biophys Acta 410:333–346
Kim T, Gu B, Jeong J, Byun S, Shin Y (1995) Purification and characterization of a maltotetraose-forming alkaline (alpha)-amylase from an alkalophilic bacillus strain, GM8901. Appl Environ Microbiol 61:3105–3112
Klibanov A (1997) Why are enzymes less active in organic solvents than in water? Trends Biotechnol 15:97–101
Kobayashi T, Kanai H, Hayashi T, Akiba T, Akaboshi R, Horikoshi K (1992) Haloalkaliphilic maltotriose-forming α-amylase from the Archaebacterium Natronococcus sp. strain Ah-36. J Bacteriol 174:3439–3444
Laane C, Boeren S, Vos K, Veegar C (1987) Rules for optimization of biocatalysis in solvents. Biotechnol Bioeng 30:81–87
Laemmli U (1970) Cleavage of structural proteins during assembly of the head of bacteriophage T4. Nature 224:680–685
Lane D, Pace B, Olsen G, Stahl D, Sogin M, Pace N (1985) Rapid determination of 16S ribosomal RNA sequences for phylogenetic analysis. Proc Natl Acad Sci USA 82:6955–6959
Lee Y, Kim H (1991) Enhancement of enzymatic production of cyclodextrins by organic solvents. Enzyme Microb Technol 13:499–503
Messaoud E, Ali M, Elleuch N, Masmoudi N, Bejar S (2004) Purification and properties of a maltoheptaose- and maltohexaose-forming amylase produced by Bacillus subtilis US116. Enzyme Microb Technol 34:662–666
Miller GL (1959) Use of dinitro salicylic acid reagent for determination of reducing sugar. Anal Chem 31:426–428
Morgan F, Priest F (1981) Characterization of a thermostable α-amylase from Bacillus licheniformis NCIB 6346. J Appl Bacteriol 50:107–114
Nagarajan D, Rajagopalan G, Krishnan C (2006) Purification and characterization of a maltooligosaccharide-forming alpha-amylase from a new Bacillus subtilis KCC103. Appl Microbiol Biotechnol 73:591–597
Ogino H, Miyamoto K, Ishikawa H (1994) Organic-solvent-tolerant bacterium which secretes organic- solvent-stable lipolytic enzyme. Appl Environ Microbiol 64:1929–1932
Ogino H, Yasui K, Shinotani T, Ishihara T, Ishikawa H (1995) Organic solvent-tolerant bacterium which secretes an organic solvent-stable proteolytic enzyme. Appl Environ Microbiol 61:4258–4262
Park K (1992) Development of new carbohydrate materials. Food Sci Ind 25:73–82
Robyt J, Ackerman R (1971) Isolation, purification, and characterization of a maltotetraose-producing amylase from Pseudomonas stutzeri. Arch Biochem Biophys 145:105–114
Satoh E, Uchimura T, Kudo T, Komagata K (1997) Purification, characterization, and nucleotide sequence of an intracellular maltotriose-producing α-amylase from Streptococcus bovis 148. Appl Environ Microbiol 63:4941–4944
Takasaki Y (1985) An amylase producing maltotriose from Bacillus subtilis. Agric Biol Chem 49:1091–1097
Takasaki Y, Kitajima M, Tsuruta T, Nonoguchi M, Hayashi S, Imada K (1991a) Maltotriose-producing amylase from Microbacterium imperiale. Agric Biol Chem 55:687–692
Takasaki Y, Shinohara H, Tsuruhisa M, Hayashi S, Imada K (1991b) Maltotetraose-producing amylase from Bacillus sp. MG-4. Agric Biol Chem 55:1715–1720
Tonkova A (1998) Bacterial cyclodextrin glucanotransferase. Enzyme Microb Technol 22:678–686
Wako K, Takahashi S, Hashimoto S, Kanaeda J (1978) Studies on maltotriose- and maltose-forming amylases from Streptomyces. J Jpn Soc Starch Sci 25:155–161
Yang C, Liu W (2004) Purification and properties of a maltotriose-producing α-amylase from Thermobifida fusca. Enzyme Microb Technol 35:254–260
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This work was supported in part by the Industrial Technology Research Grant Program in 2005 from New Energy and Industrial Technology Development Organization (NEDO) of Japan, the INOUE ENRYO Memorial Foundation for the Promotion of Sciences, and the Grant for the High Tech Research Center Program organized by Ministry of Education, Culture, Sports, Science and Technology of Japan since 2006.
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Doukyu, N., Yamagishi, W., Kuwahara, H. et al. Purification and characterization of a maltooligosaccharide-forming amylase that improves product selectivity in water-miscible organic solvents, from dimethylsulfoxide-tolerant Brachybacterium sp. strain LB25. Extremophiles 11, 781–788 (2007). https://doi.org/10.1007/s00792-007-0096-8
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DOI: https://doi.org/10.1007/s00792-007-0096-8


