Directed evolution of thermostable kanamycin-resistance gene:: A convenient selection marker for Thermus thermophilus

被引:136
作者
Hoseki, J
Yano, T
Koyama, Y
Kuramitsu, S
Kagamiyama, H [1 ]
机构
[1] Osaka Med Coll, Dept Biochem, Takatsuki, Osaka 5698686, Japan
[2] Osaka Univ, Grad Sch Sci, Dept Biol, Toyonaka, Osaka 5600043, Japan
[3] MITI, Agcy Ind Sci & Technol, Natl Inst Biosci & Human Technol, Tsukuba, Ibaraki 3058566, Japan
关键词
directed evolution; DNA shuffling; kanamycin-resistance gene; thermostability; Thermus thermophilus;
D O I
10.1093/oxfordjournals.jbchem.a022539
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
The whole-genome sequencing of an extreme thermophile, Thermus thermophilus, is now in progress, Like other genome projects, major concern is shifting from the sequence itself to post-sequencing research such as functional or structural genomics, Under such circumstances, the demand for convenient genetic-engineering tools is increasing. Tn this study we have increased the thermostability of a kanamycin-resistance gene product using strategies based on directed evolution in T. thermophilus to the upper limit of its growth temperature. The most thermostable mutant has 19 amino-acid substitutions, whereby the thermostability is increased by 20 degrees C, but the enzymatic activity is not significantly changed. Most of the mutated residues are located on the surface of the protein molecule, and, interestingly, five of the 19 substitutions are those to proline residues, The evolved kanamycin-resistance gene products could be used as selection markers at the optimum growth temperature of T. thermophilus, The development of such a convenient genetic-engineering tool would facilitate post-sequencing research on T. thermophilus.
引用
收藏
页码:951 / 956
页数:6
相关论文
共 33 条
[1]   A GENETIC SCREEN FOR MUTATIONS THAT INCREASE THE THERMAL-STABILITY OF PHAGE-T4 LYSOZYME [J].
ALBER, T ;
WOZNIAK, JA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1985, 82 (03) :747-750
[2]  
ARGOS P, 1979, BIOCHEISTRY, V18, P5968
[3]   Improved properties of FLP recombinase evolved by cycling mutagenesis [J].
Buchholz, F ;
Angrand, PO ;
Stewart, AF .
NATURE BIOTECHNOLOGY, 1998, 16 (07) :657-662
[4]   DRAMATIC THERMOSTABILIZATION OF YEAST ISO-1-CYTOCHROME-C BY AN ASPARAGINE-]ISOLEUCINE REPLACEMENT AT POSITION-57 [J].
DAS, G ;
HICKEY, DR ;
MCLENDON, D ;
MCLENDON, G ;
SHERMAN, F .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (02) :496-499
[5]   PLASMID-DETERMINED RESISTANCE TO ANTI-MICROBIAL AGENTS [J].
DAVIES, J ;
SMITH, DI .
ANNUAL REVIEW OF MICROBIOLOGY, 1978, 32 :469-518
[6]   Directed evolution of a thermostable esterase [J].
Giver, L ;
Gershenson, A ;
Freskgard, PO ;
Arnold, FH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (22) :12809-12813
[7]   MAPPING THE STABILITY DETERMINANTS OF BACTERIAL TYROSYL-TRANSFER RNA-SYNTHETASES BY AN EXPERIMENTAL EVOLUTIONARY APPROACH [J].
GUEZIVANIER, V ;
HERMANN, M ;
BALDWIN, D ;
BEDOUELLE, H .
JOURNAL OF MOLECULAR BIOLOGY, 1993, 234 (01) :209-221
[8]   PLASMID MARKER RESCUE TRANSFORMATION IN THERMUS-THERMOPHILUS [J].
HOSHINO, T ;
MASEDA, H ;
NAKAHARA, T .
JOURNAL OF FERMENTATION AND BIOENGINEERING, 1993, 76 (04) :276-279
[9]   DESIGN AND STRUCTURAL-ANALYSIS OF ALTERNATIVE HYDROPHOBIC CORE PACKING ARRANGEMENTS IN BACTERIOPHAGE-T4 LYSOZYME [J].
HURLEY, JH ;
BAASE, WA ;
MATTHEWS, BW .
JOURNAL OF MOLECULAR BIOLOGY, 1992, 224 (04) :1143-1159
[10]   A NEW WAY OF ENHANCING THE THERMOSTABILITY OF PROTEASES [J].
IMANAKA, T ;
SHIBAZAKI, M ;
TAKAGI, M .
NATURE, 1986, 324 (6098) :695-697