Abstract
The nucleotide sequence of the gene coding for xylose isomerase from Ampullariella sp. strain 3876, a gram-positive bacterium, has been determined. A clone of a fragment of strain 3876 DNA coding for a xylose isomerase activity was identified by its ability to complement a xylose isomerase-defective Escherichia coli strain. One such complementation positive fragment, 2,922 nucleotides in length, was sequenced in its entirety. There are two open reading frames 1,182 and 1,242 nucleotides in length, on opposite strands of this fragment, each of which could code for a protein the expected size of xylose isomerase. The 1,182-nucleotide open reading frame was identified as the coding sequence for the protein from the sequence analysis of the amino-terminal region and selected internal peptides. The gene initiates with GTG and has a high guanine and cytosine content (70%) and an exceptionally strong preference (97%) for guanine or cytosine in the third position of the codons. The gene codes for a 43,210-dalton polypeptide composed of 393 amino acids. The xylose isomerase from Ampullariella sp. strain 3876 is similar in size to other bacterial xylose isomerases and has limited amino acid sequence homology to the available sequences from E. coli, Bacillus subtilis, and Streptomyces violaceus-ruber. In all cases yet studied, the bacterial gene for xylulose kinase is downstream from the gene for xylose isomerase. We present evidence suggesting that in Ampullariella sp. strain 3876 these genes are similarly arranged.
Full text
PDFSelected References
These references are in PubMed. This may not be the complete list of references from this article.
- Ahlem C., Huisman W., Neslund G., Dahms A. S. Purification and properties of a periplasmic D-xylose-binding protein from Escherichia coli K-12. J Biol Chem. 1982 Mar 25;257(6):2926–2931. [PubMed] [Google Scholar]
- Bolivar F., Rodriguez R. L., Greene P. J., Betlach M. C., Heyneker H. L., Boyer H. W., Crosa J. H., Falkow S. Construction and characterization of new cloning vehicles. II. A multipurpose cloning system. Gene. 1977;2(2):95–113. [PubMed] [Google Scholar]
- David J. D., Wiesmeyer H. Control of xylose metabolism in Escherichia coli. Biochim Biophys Acta. 1970 Mar 24;201(3):497–499. doi: 10.1016/0304-4165(70)90171-6. [DOI] [PubMed] [Google Scholar]
- Dunn R., McCoy J., Simsek M., Majumdar A., Chang S. H., Rajbhandary U. L., Khorana H. G. The bacteriorhodopsin gene. Proc Natl Acad Sci U S A. 1981 Nov;78(11):6744–6748. doi: 10.1073/pnas.78.11.6744. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ensign J. C. Formation, properties, and germination of actinomycete spores. Annu Rev Microbiol. 1978;32:185–219. doi: 10.1146/annurev.mi.32.100178.001153. [DOI] [PubMed] [Google Scholar]
- Farina G., Bradley S. G. Reassociation of deoxyribonucleic acids from Actinoplanes and other actinomycetes. J Bacteriol. 1970 Apr;102(1):30–35. doi: 10.1128/jb.102.1.30-35.1970. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Ghangas G. S., Wilson D. B. Isolation and characterization of the Salmonella typhimurium LT2 xylose regulon. J Bacteriol. 1984 Jan;157(1):158–164. doi: 10.1128/jb.157.1.158-164.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Gold L., Pribnow D., Schneider T., Shinedling S., Singer B. S., Stormo G. Translational initiation in prokaryotes. Annu Rev Microbiol. 1981;35:365–403. doi: 10.1146/annurev.mi.35.100181.002053. [DOI] [PubMed] [Google Scholar]
- Ikai A. Thermostability and aliphatic index of globular proteins. J Biochem. 1980 Dec;88(6):1895–1898. [PubMed] [Google Scholar]
- Kagawa Y., Nojima H., Nukiwa N., Ishizuka M., Nakajima T., Yasuhara T., Tanaka T., Oshima T. High guanine plus cytosine content in the third letter of codons of an extreme thermophile. DNA sequence of the isopropylmalate dehydrogenase of Thermus thermophilus. J Biol Chem. 1984 Mar 10;259(5):2956–2960. [PubMed] [Google Scholar]
- Lawlis V. B., Dennis M. S., Chen E. Y., Smith D. H., Henner D. J. Cloning and sequencing of the xylose isomerase and xylulose kinase genes of Escherichia coli. Appl Environ Microbiol. 1984 Jan;47(1):15–21. doi: 10.1128/aem.47.1.15-21.1984. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Maleszka R., Wang P. Y., Schneider H. A Col E1 hybrid plasmid containing Escherichia coli genes complementing d-xylose negative mutants of Escherichia coli and Salmonella typhimurium. Can J Biochem. 1982 Feb;60(2):144–151. doi: 10.1139/o82-020. [DOI] [PubMed] [Google Scholar]
- Maxam A. M., Gilbert W. Sequencing end-labeled DNA with base-specific chemical cleavages. Methods Enzymol. 1980;65(1):499–560. doi: 10.1016/s0076-6879(80)65059-9. [DOI] [PubMed] [Google Scholar]
- Mills D. R., Kramer F. R. Structure-independent nucleotide sequence analysis. Proc Natl Acad Sci U S A. 1979 May;76(5):2232–2235. doi: 10.1073/pnas.76.5.2232. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Norrander J., Kempe T., Messing J. Construction of improved M13 vectors using oligodeoxynucleotide-directed mutagenesis. Gene. 1983 Dec;26(1):101–106. doi: 10.1016/0378-1119(83)90040-9. [DOI] [PubMed] [Google Scholar]
- Parenti F., Coronelli C. Members of the genus Actinoplanes and their antibiotics. Annu Rev Microbiol. 1979;33:389–411. doi: 10.1146/annurev.mi.33.100179.002133. [DOI] [PubMed] [Google Scholar]
- Robbins P. W., Trimble R. B., Wirth D. F., Hering C., Maley F., Maley G. F., Das R., Gibson B. W., Royal N., Biemann K. Primary structure of the Streptomyces enzyme endo-beta-N-acetylglucosaminidase H. J Biol Chem. 1984 Jun 25;259(12):7577–7583. [PubMed] [Google Scholar]
- Rosenberg M., Court D. Regulatory sequences involved in the promotion and termination of RNA transcription. Annu Rev Genet. 1979;13:319–353. doi: 10.1146/annurev.ge.13.120179.001535. [DOI] [PubMed] [Google Scholar]
- Sanger F., Coulson A. R., Barrell B. G., Smith A. J., Roe B. A. Cloning in single-stranded bacteriophage as an aid to rapid DNA sequencing. J Mol Biol. 1980 Oct 25;143(2):161–178. doi: 10.1016/0022-2836(80)90196-5. [DOI] [PubMed] [Google Scholar]
- Schellenberg G. D., Sarthy A., Larson A. E., Backer M. P., Crabb J. W., Lidstrom M., Hall B. D., Furlong C. E. Xylose isomerase from Escherichia coli. Characterization of the protein and the structural gene. J Biol Chem. 1984 Jun 10;259(11):6826–6832. [PubMed] [Google Scholar]
- Shamanna D. K., Sanderson K. E. Uptake and catabolism of D-xylose in Salmonella typhimurium LT2. J Bacteriol. 1979 Jul;139(1):64–70. doi: 10.1128/jb.139.1.64-70.1979. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Shine J., Dalgarno L. The 3'-terminal sequence of Escherichia coli 16S ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites. Proc Natl Acad Sci U S A. 1974 Apr;71(4):1342–1346. doi: 10.1073/pnas.71.4.1342. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Smith H. O. Recovery of DNA from gels. Methods Enzymol. 1980;65(1):371–380. doi: 10.1016/s0076-6879(80)65048-4. [DOI] [PubMed] [Google Scholar]
- Wilhelm M., Hollenberg C. P. Selective cloning of Bacillus subtilis xylose isomerase and xylulokinase in Escherichia coli genes by IS5-mediated expression. EMBO J. 1984 Nov;3(11):2555–2560. doi: 10.1002/j.1460-2075.1984.tb02173.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Wovcha M. G., Steuerwald D. L., Brooks K. E. Amplification of D-xylose and D-glucose isomerase activities in Escherichia coli by gene cloning. Appl Environ Microbiol. 1983 Apr;45(4):1402–1404. doi: 10.1128/aem.45.4.1402-1404.1983. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Yip Y. K., Waks M., Beychok S. Reconstitution of native human hemoglobin from separated globin chains and alloplex intermediates. Proc Natl Acad Sci U S A. 1977 Jan;74(1):64–68. doi: 10.1073/pnas.74.1.64. [DOI] [PMC free article] [PubMed] [Google Scholar]