Membrane-bound amylopullulanase is essential for starch metabolism of Sulfolobus acidocaldarius DSM639

被引:17
作者
Choi, Kyoung-Hwa [1 ]
Cha, Jaeho [1 ]
机构
[1] Pusan Natl Univ, Coll Nat Sci, Dept Microbiol, Busan 609735, South Korea
基金
新加坡国家研究基金会;
关键词
Amylopullulanase; Sulfolobales; Archaea; Maltose/maltodextrin operon; HYPERTHERMOPHILIC ARCHAEON; PYROCOCCUS-FURIOSUS; THERMOCOCCUS-HYDROTHERMALIS; ABC TRANSPORTERS; SOLFATARICUS; SUGAR; GENE; IDENTIFICATION; PURIFICATION; ENZYMES;
D O I
10.1007/s00792-015-0766-x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Sulfolobus acidocaldarius DSM639 produced an acid-resistant membrane-bound amylopullulanase (Apu) during growth on starch as a sole carbon and energy source. The physiological role of Apu in starch metabolism was investigated by the growth and starch degradation pattern of apu disruption mutant as well as biochemical properties of recombinant Apu. The Delta apu mutant lost the ability to grow in minimal medium in the presence of starch, and the amylolytic activity observed in the membrane fraction of the wild-type strain was not detected in the Delta apu mutant when the cells were grown in YT medium. The purified membrane-bound Apu initially hydrolyzed starch, amylopectin, and pullulan into various sizes of maltooligosaccharides, and then produced glucose, maltose, and maltotriose in the end, indicating Apu is a typical endo-acting glycoside hydrolase family 57 (GH57) amylopullulanase. The maltose and maltotriose observed in the culture medium during the exponential and stationary phase growth indicates that Apu is the essential enzyme to initially hydrolyze the starch into small maltooligosaccharides to be transported into the cell.
引用
收藏
页码:909 / 920
页数:12
相关论文
共 25 条
[1]   Prediction of signal peptides in archaea [J].
Bagos, P. G. ;
Tsirigos, K. D. ;
Plessas, S. K. ;
Liakopoulos, T. D. ;
Hamodrakas, S. J. .
PROTEIN ENGINEERING DESIGN & SELECTION, 2009, 22 (01) :27-35
[2]   Sequence fingerprints of enzyme specificities from the glycoside hydrolase family GH57 [J].
Blesak, Karol ;
Janecek, Stefan .
EXTREMOPHILES, 2012, 16 (03) :497-506
[3]  
BRADFORD MM, 1976, ANAL BIOCHEM, V72, P248, DOI 10.1016/0003-2697(76)90527-3
[4]   VERY STABLE ENZYMES FROM EXTREMELY THERMOPHILIC ARCHAEBACTERIA AND EUBACTERIA [J].
BRAGGER, JM ;
DANIEL, RM ;
COOLBEAR, T ;
MORGAN, HW .
APPLIED MICROBIOLOGY AND BIOTECHNOLOGY, 1989, 31 (5-6) :556-561
[5]   CHARACTERIZATION OF AMYLOLYTIC ENZYMES, HAVING BOTH ALPHA-1,4 AND ALPHA-1,6 HYDROLYTIC ACTIVITY, FROM THE THERMOPHILIC ARCHAEA PYROCOCCUS-FURIOSUS AND THERMOCOCCUS-LITORALIS [J].
BROWN, SH ;
KELLY, RM .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1993, 59 (08) :2614-2621
[6]   Identification and Characterization of MalA in the Maltose/Maltodextrin Operon of Sulfolobus acidocaldarius DSM639 [J].
Choi, Kyoung-Hwa ;
Hwang, Sungmin ;
Cha, Jaeho .
JOURNAL OF BACTERIOLOGY, 2013, 195 (08) :1789-1799
[7]   GLUCOSE-METABOLISM IN THE EXTREME THERMOACIDOPHILIC ARCHAEBACTERIUM SULFOLOBUS-SOLFATARICUS [J].
DEROSA, M ;
GAMBACORTA, A ;
NICOLAUS, B ;
GIARDINA, P ;
POERIO, E ;
BUONOCORE, V .
BIOCHEMICAL JOURNAL, 1984, 224 (02) :407-414
[8]   Cloning, sequencing, and expression of the gene encoding amylopullulanase from Pyrococcus furiosus and biochemical characterization of the recombinant enzyme [J].
Dong, GQ ;
Vieille, C ;
Zeikus, JG .
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, 1997, 63 (09) :3577-3584
[9]   Sugar transport in Sulfolobus solfataricus is mediated by two families of binding protein-dependent ABC transporters [J].
Elferink, MGL ;
Albers, SV ;
Konings, WN ;
Driessen, AJM .
MOLECULAR MICROBIOLOGY, 2001, 39 (06) :1494-1503
[10]   Comparative study of the extracellular proteome of Sulfolobus species reveals limited secretion [J].
Ellen, Albert F. ;
Albers, Sonja-Verena ;
Driessen, Arnold J. M. .
EXTREMOPHILES, 2010, 14 (01) :87-98