Functional myo-inositol catabolic genes of Bacillus subtilis natto are involved in depletion of pinitol in natto (Fermented soybean)

被引:12
作者
Morinaga, Tetsuro
Yamaguchi, Masanori
Makino, Yuki
Nanamiya, Hideaki
Takahashi, Kiwamu
Yoshikawa, Hirofumi
Kawamura, Fujio
Ashida, Hitoshi
Yoshida, Ken-ichi [1 ]
机构
[1] Kobe Univ, Fac Agr, Dept Biofunct Chem, Kobe, Hyogo 6578501, Japan
[2] Hokko Chem Ind Co Ltd, Cent Res Labs, Atsugi, Kanagawa 2430023, Japan
[3] Rikkyo Univ, Coll Sci, Mol Genet Lab, Tokyo 1718501, Japan
[4] Tokyo Univ Agr, Dept Biosci, Tokyo 1568502, Japan
关键词
Bacillus subtilis; natto; pinitol; myo-inositol;
D O I
10.1271/bbb.60084
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
Soybeans are rich in pinitol (PI; 3-O-methyl-D-chiroinositol), which improves health by treating conditions associated with insulin resistance, such as diabetes mellitus and obesity. Natto is a food made from soybeans fermented by strains of Bacillus subtilis natto. In the chromosome of natto strain OK2, there is a putative promoter region almost identical to the iol promoter for myo-inositol (MI) catabolic genes of B. subtilis 168. In the presence of MI, the putative iol promoter functioned to induce inositol dehydrogenase, the enzyme for the first-step reaction in the MI catabolic pathway. PI also induced inositol dehydrogenase and the promoter was indispensable for the utilization of PI as well as MI, suggesting that PI might be an alternative carbon source metabolized in a way involving the MI catabolic genes. Natto fermentation studies have revealed that the parental natto strain consumed PI while a mutant defective in the iol promoter did not do so at all. These results suggest that inactivating the MI catabolic genes might prevent PI consumption, retaining it in natto for enrichment of possible health-promoting properties.
引用
收藏
页码:1913 / 1920
页数:8
相关论文
共 25 条
[1]  
ANDERSON WA, 1971, J BIOL CHEM, V246, P5662
[2]   Natural genetic competence in Bacillus subtilis natto OK2 [J].
Ashikaga, S ;
Nanamiya, H ;
Ohashi, Y ;
Kawamura, F .
JOURNAL OF BACTERIOLOGY, 2000, 182 (09) :2411-2415
[3]   Differences in effects on DNA gyrase activity between two glutamate racemases of Bacillus subtilis, the poly-γ-glutamate synthesis-linking Glr enzyme and the YrpC (MurI) isozyme [J].
Ashiuchi, M ;
Kuwana, E ;
Komatsu, K ;
Soda, K ;
Misono, H .
FEMS MICROBIOLOGY LETTERS, 2003, 223 (02) :221-225
[4]   Physiological and biochemical characteristics of poly γ-glutamate synthetase complex of Bacillus subtilis [J].
Ashiuchi, M ;
Nawa, C ;
Kamei, T ;
Song, JJ ;
Hong, SP ;
Sung, MH ;
Soda, K ;
Yagi, T ;
Misono, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2001, 268 (20) :5321-5328
[5]   Insulin-like effect of pinitol [J].
Bates, SH ;
Jones, RB ;
Bailey, CJ .
BRITISH JOURNAL OF PHARMACOLOGY, 2000, 130 (08) :1944-1948
[6]   INDUCED BIOCHEMICAL MUTATIONS IN BACILLUS-SUBTILIS [J].
BURKHOLDER, PR ;
GILES, NH .
AMERICAN JOURNAL OF BOTANY, 1947, 34 (06) :345-348
[7]   ISOLATION AND PROPERTIES OF A BACILLUS-SUBTILIS MUTANT UNABLE TO PRODUCE FRUCTOSE-BISPHOSPHATASE [J].
FUJITA, Y ;
FREESE, E .
JOURNAL OF BACTERIOLOGY, 1981, 145 (02) :760-767
[8]  
FUJITA Y, 1991, GENE, V108, P121
[9]   SELECTIVE AMPLIFICATION OF CDNA SEQUENCE FROM TOTAL RNA BY CASSETTE-LIGATION MEDIATED POLYMERASE CHAIN-REACTION (PCR) - APPLICATION TO SEQUENCING 6.5 KB GENOME SEGMENT OF HANTAVIRUS STRAIN B-1 [J].
ISEGAWA, Y ;
SHENG, J ;
SOKAWA, Y ;
YAMANISHI, K ;
NAKAGOMI, O ;
UEDA, S .
MOLECULAR AND CELLULAR PROBES, 1992, 6 (06) :467-475
[10]   Glr, a glutamate racemase, supplies D-glutamate to both peptidoglycan synthesis and poly-γ-glutamate production in γ-PGA-producing Bacillus subtilis [J].
Kada, S ;
Nanamiya, H ;
Kawamura, F ;
Horinouchi, S .
FEMS MICROBIOLOGY LETTERS, 2004, 236 (01) :13-20