Diversity of Beta-Propeller Phytase Genes in the Intestinal Contents of Grass Carp Provides Insight into the Release of Major Phosphorus from Phytate in Nature

被引:86
作者
Huang, Huoqing [1 ]
Shi, Pengjun [1 ]
Wang, Yaru [1 ]
Luo, Huiying [1 ]
Shao, Na [1 ]
Wang, Guozeng [1 ]
Yang, Peilong [1 ]
Yao, Bin [1 ]
机构
[1] Chinese Acad Agr Sci, Feed Res Inst, Key Lab Feed Biotechnol, Minist Agr, Beijing 100081, Peoples R China
基金
国家高技术研究发展计划(863计划);
关键词
INOSITOL HEXAPHOSPHATE; BACTERIA; PCR; AMPLIFICATION; PURIFICATION; CLONING; GROWTH; NOV; DNA;
D O I
10.1128/AEM.02188-08
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Phytate is the most abundant organic phosphorus compound in nature, and microbial mineralization of phytate by phytase is a key process for phosphorus recycling in the biosphere. In the present study, beta-propeller phytase (BPP) gene fragments were readily amplified from the intestinal contents of grass carp (Ctenopharyngodon idellus) directly or from phytate-degrading isolates from the same source, confirming the widespread occurrence of BPP in aquatic communities. The amounts of sequences collected using these two methods differed (88 distinct genes versus 10 isolates), but the sequences showed the same general topology based on phylogenetic analysis. All of the sequences fell in five clusters and were distinct from those of Anabaena, Gloeobacter, Streptomyces, Flavobacterium, Prosthecochloris, and Desulfuromonas, which have never been found in the grass carp intestine. Analysis of the microbial diversity by denaturing gradient gel electrophoresis demonstrated that unculturable bacteria were dominant bacteria in the grass carp intestine and thus the predominant phytate-degrading organisms. The predominant cultured species corresponding to the phytate-degrading isolates, Pseudomonas, Bacillus and Shewanella species, might be the main source of known BPPs. A phytase from Brevundimonas was first obtained from cultured species. Combining our results with Lim et al.'s inference that phytate-mineralizing bacteria are widely distributed and highly diverse in nature (B. L. Lim, P. Yeung, C. Cheng, and J. E. Hill, ISME J. 1:321-330, 2007), we concluded that BPP is the major phytate-degrading enzyme in nature, that most of this enzyme might originate from unculturable bacteria, and that the distribution of BPP may be related to the type of niche. To our knowledge, this is the first study to experimentally estimate BPP diversity in situ.
引用
收藏
页码:1508 / 1516
页数:9
相关论文
共 43 条
  • [1] AOE H., 1967, Bulletin of the Japanese Society for the Science of Fish, V33, P674, DOI DOI 10.2331/SUISAN.33.674
  • [2] Beta-propeller phytases in the aquatic environment
    Cheng, CW
    Lim, BL
    [J]. ARCHIVES OF MICROBIOLOGY, 2006, 185 (01) : 1 - 13
  • [3] Coates JD, 1995, ARCH MICROBIOL, V164, P406
  • [4] The Ribosomal Database Project (RDP-II): sequences and tools for high-throughput rRNA analysis
    Cole, JR
    Chai, B
    Farris, RJ
    Wang, Q
    Kulam, SA
    McGarrell, DM
    Garrity, GM
    Tiedje, JM
    [J]. NUCLEIC ACIDS RESEARCH, 2005, 33 : D294 - D296
  • [5] A NEW PHOTOTROPHIC GREEN SULPHUR BACTERIUM - PROSTHECOCHLORIS-AESTUARII NOV-GEN. NOV-SPEC.
    GORLENKO, VM
    [J]. ZEITSCHRIFT FUR ALLGEMEINE MIKROBIOLOGIE, 1970, 10 (02): : 147 - &
  • [6] Purification and characterization of a phytase from Klebsiella terrigena
    Greiner, R
    Haller, E
    Konietzny, U
    Jany, KD
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1997, 341 (02) : 201 - 206
  • [7] Ha NC, 2000, NAT STRUCT BIOL, V7, P147
  • [8] Metagenomic approach for the isolation of a novel low-temperature-active lipase from uncultured bacteria of marine sediment
    Hardeman, Fredrik
    Sjoling, Sara
    [J]. FEMS MICROBIOLOGY ECOLOGY, 2007, 59 (02) : 524 - 534
  • [9] Isolation and assessment of phytate-hydrolysing bacteria from the DelMarVa Peninsula
    Hill, Jane E.
    Kysela, David
    Elimelech, Menachem
    [J]. ENVIRONMENTAL MICROBIOLOGY, 2007, 9 (12) : 3100 - 3107
  • [10] A novel phytase with preferable characteristics from Yersinia intermedia
    Huang, Huoqing
    Luo, Huiying
    Yang, Peilong
    Meng, Kun
    Wang, Yaru
    Yuan, Tiezheng
    Bai, Yingguo
    Yao, Bin
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2006, 350 (04) : 884 - 889