Expanding tryptophan-containing cyclodipeptide synthase spectrum by identification of nine members from Streptomyces strains
Cyclodipeptide synthases (CDPSs) comprise normally 200–300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector an...
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Published in | Applied microbiology and biotechnology Vol. 102; no. 10; pp. 4435 - 4444 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
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Berlin/Heidelberg
Springer Berlin Heidelberg
01.05.2018
Springer Springer Nature B.V |
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Abstract | Cyclodipeptide synthases (CDPSs) comprise normally 200–300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight
Streptomyces
strains were cloned into pET28a vector and expressed in
Escherichia coli
. Structural elucidation of the isolated products led to the identification of one
cyclo
-
l
-Trp-
l
-Leu, two
cyclo
-
l
-Trp-
l
-Pro, and three
cyclo
-
l
-Trp-
l
-Trp synthases. Other three CDPSs produce
cyclo
-
l
-Trp-
l
-Ala or
cyclo
-
l
-Trp-
l
-Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L
E. coli
culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology. |
---|---|
AbstractList | Cyclodipeptide synthases (CDPSs) comprise normally 200–300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector and expressed in Escherichia coli. Structural elucidation of the isolated products led to the identification of one cyclo-l-Trp-l-Leu, two cyclo-l-Trp-l-Pro, and three cyclo-l-Trp-l-Trp synthases. Other three CDPSs produce cyclo-l-Trp-l-Ala or cyclo-l-Trp-l-Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L E. coli culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology. Cyclodipeptide synthases (CDPSs) comprise normally 200–300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector and expressed in Escherichia coli . Structural elucidation of the isolated products led to the identification of one cyclo - l -Trp- l -Leu, two cyclo - l -Trp- l -Pro, and three cyclo - l -Trp- l -Trp synthases. Other three CDPSs produce cyclo - l -Trp- l -Ala or cyclo - l -Trp- l -Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L E. coli culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology. Cyclodipeptide synthases (CDPSs) comprise normally 200-300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector and expressed in Escherichia coli. Structural elucidation of the isolated products led to the identification of one cyclo-L-Trp-L-Leu, two cyclo-L-Trp-L-Pro, and three cyclo-L-Trp-L-Trp synthases. Other three CDPSs produce cyclo-L-Trp-L-Ala or cyclo-L-Trp-L-Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L E. coli culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology.Cyclodipeptide synthases (CDPSs) comprise normally 200-300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector and expressed in Escherichia coli. Structural elucidation of the isolated products led to the identification of one cyclo-L-Trp-L-Leu, two cyclo-L-Trp-L-Pro, and three cyclo-L-Trp-L-Trp synthases. Other three CDPSs produce cyclo-L-Trp-L-Ala or cyclo-L-Trp-L-Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L E. coli culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology. Cyclodipeptide synthases (CDPSs) comprise normally 200-300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal machinery for cyclodipeptide formation. In this study, nine new CDPS genes from eight Streptomyces strains were cloned into pET28a vector and expressed in Escherichia coli. Structural elucidation of the isolated products led to the identification of one cyclo-L-Trp-L-Leu, two cyclo-L-Trp-L-Pro, and three cyclo-L-Trp-L-Trp synthases. Other three CDPSs produce cyclo-L-Trp-L-Ala or cyclo-L-Trp-L-Tyr as the major cyclodipeptide. Total product yields of 46 to 211 mg/L E. coli culture were obtained. Our findings represent rare examples of CDPS family derived from actinobacteria that form various tryptophan-containing cyclodipeptides. Furthermore, this study highlights the potential of the microbial machinery for tryptophan-containing cyclodipeptide biosynthesis and provides valid experimental basis for further combination of these CDPS genes with other modification genes in synthetic biology. |
Audience | Academic |
Author | Liu, Jing Li, Shu-Ming Yu, Huili |
Author_xml | – sequence: 1 givenname: Jing surname: Liu fullname: Liu, Jing organization: Institut für Pharmazeutische Biologie und Biotechnologie, Philipps-Universität Marburg – sequence: 2 givenname: Huili surname: Yu fullname: Yu, Huili organization: Institut für Pharmazeutische Biologie und Biotechnologie, Philipps-Universität Marburg – sequence: 3 givenname: Shu-Ming orcidid: 0000-0003-4583-2655 surname: Li fullname: Li, Shu-Ming email: shuming.li@staff.uni-marburg.de organization: Institut für Pharmazeutische Biologie und Biotechnologie, Philipps-Universität Marburg |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/29574613$$D View this record in MEDLINE/PubMed |
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Keywords | Cyclodipeptide synthase Tryptophan-containing cyclodipeptide Aminoacyl t-RNA Diketopiperazine Streptomyces |
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Snippet | Cyclodipeptide synthases (CDPSs) comprise normally 200–300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal... Cyclodipeptide synthases (CDPSs) comprise normally 200-300 amino acid residues and are mainly found in bacteria. They hijack aminoacyl-tRNAs from the ribosomal... |
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SubjectTerms | Amino acids Bacteria Biomedical and Life Sciences Biosynthesis Biotechnologically Relevant Enzymes and Proteins Biotechnology Cloning DNA methylation E coli Enzymes Escherichia coli Escherichia coli - genetics Fungi Gene expression Genes Life Sciences Machinery and equipment Microbial Genetics and Genomics Microbiology Microorganisms Peptide Synthases - chemistry Peptide Synthases - genetics Peptide Synthases - isolation & purification Peptides Physiological aspects Plasmids Strains (organisms) Streptomyces Streptomyces - classification Streptomyces - enzymology Synthetic biology Transfer RNA Tryptophan Tryptophan - genetics |
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Title | Expanding tryptophan-containing cyclodipeptide synthase spectrum by identification of nine members from Streptomyces strains |
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