Cellulase genes from the parabasalian symbiont Pseudotrichonympha grassii in the hindgut of the wood-feeding termite Coptotermes formosanus

被引:64
作者
Nakashima, K
Watanabe, H [1 ]
Azuma, JI
机构
[1] Natl Inst Agrobiol Sci, Tsukuba, Ibaraki 3058634, Japan
[2] Kyoto Univ, Grad Sch Agr, Div Environm Sci & Technol, Sakyo Ku, Kyoto 6068502, Japan
关键词
cellulase; Pseudotrichonympha grassii; parabasalia; symbiosis; termite; Coptotermes formosanus; glycoside hydrolase family 7;
D O I
10.1007/s00018-002-8528-1
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
Cellulase genes of Pseudotrichonympha grassii (Hypermastigida: Eucomonymphidae), the symbiotic flagellate in the hindgut of the wood-feeding termite Coptotermes formosanus, were isolated and characterized. The nucleotide sequences of the major cellulase component in the hindgut of C. formosanus were determined based on its N-terminal amino acid sequence. The five isolated nucleotide sequences (PgCBH-homos) had an open reading frame of 1350 bp showing similarity to catalytic domains of glycoside hydrolase family (GHF) 7 members, and primary structure comparison with GHF7 members whose tertiary structures are well-characterized revealed the overall similarity between PgCBH-homo and the catalytic domain of a processive cellulase Cel7A (formerly CBHI) from the aerobic fungus Trichoderma reesei. Functional expression of PgCBH-homos in Escherichia coli, using the carboxymethylcellulose-Congo red assay, demonstrated the actual cellulolytic activity of PgCBH-homo. RT-PCR showed that PgCBH-homos were expressed, from the three flagellates in the hindgut, specifically in P grassii.
引用
收藏
页码:1554 / 1560
页数:7
相关论文
共 42 条
[1]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[2]  
Bignell DE, 2000, TERMITES: EVOLUTION, SOCIALITY, SYMBIOSES, ECOLOGY, P189
[3]   ROLE OF MICROORGANISMS IN THE DIGESTION OF LIGNOCELLULOSE BY TERMITES [J].
BREZNAK, JA ;
BRUNE, A .
ANNUAL REVIEW OF ENTOMOLOGY, 1994, 39 :453-487
[4]   Microecology of the termite gut: structure and function on a microscale [J].
Brune, A ;
Friedrich, M .
CURRENT OPINION IN MICROBIOLOGY, 2000, 3 (03) :263-269
[5]   Symbiosis between termites and their intestinal protozoa [J].
Cleveland, LR .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1923, 9 :424-428
[6]  
CLEVELAND LR, 1924, BIOL BULL, V46, P177
[7]   High-resolution crystal structures reveal how a cellulose chain is bound in the 50 Å long tunnel of cellobiohydrolase I from Trichoderma reesei [J].
Divne, C ;
Ståhlberg, J ;
Teeri, TT ;
Jones, TA .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 275 (02) :309-325
[8]   THE 3-DIMENSIONAL CRYSTAL-STRUCTURE OF THE CATALYTIC CORE OF CELLOBIOHYDROLASE-I FROM TRICHODERMA-REESEI [J].
DIVNE, C ;
STAHLBERG, J ;
REINIKAINEN, T ;
RUOHONEN, L ;
PETTERSSON, G ;
KNOWLES, JKC ;
TEERI, TT ;
JONES, TA .
SCIENCE, 1994, 265 (5171) :524-528
[9]   Structural and sequence-based classification of glycoside hydrolases [J].
Henrissat, B ;
Davies, G .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 1997, 7 (05) :637-644
[10]   SYNERGISM OF CELLULASES FROM TRICHODERMA-REESEI IN THE DEGRADATION OF CELLULOSE [J].
HENRISSAT, B ;
DRIGUEZ, H ;
VIET, C ;
SCHULEIN, M .
BIO-TECHNOLOGY, 1985, 3 (08) :722-726