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1.
J Am Chem Soc ; 143(1): 132-136, 2021 01 13.
Article in English | MEDLINE | ID: mdl-33372776

ABSTRACT

We report characterization of the biosynthetic pathway of the potent immunosuppressant (-)-FR901483 (1) through heterologous expression and enzymatic assays. The biosynthetic logic to form the azatricyclic alkaloid is consistent with those proposed in biomimetic syntheses and involves aza-spiro annulation of dityrosyl-piperazine to form a ketoaldehyde intermediate, followed by regioselective aldol condensation, stereoselective ketoreduction, and phosphorylation. A possible target of 1 is proposed based on the biosynthetic studies.


Subject(s)
Immunosuppressive Agents/metabolism , Organophosphorus Compounds/metabolism , Ascomycota/genetics , Ascomycota/metabolism , Enzymes/genetics , Enzymes/metabolism , Fungal Proteins/genetics , Fungal Proteins/metabolism , Multigene Family
2.
J Antibiot (Tokyo) ; 68(8): 511-20, 2015 Aug.
Article in English | MEDLINE | ID: mdl-25783225

ABSTRACT

FR901459, a product of the fungus Stachybotrys chartarum No. 19392, is a derivative of cyclosporin A (CsA) and a powerful immunosuppressant that binds cyclophilin. Recently, it was reported that CsA was effective against hepatitis C virus (HCV). However, FR901459 lacks active moieties, which are essential for synthesizing more potent and safer derivatives of this anti-HCV agent. Here we identified an actinomycete strain (designated 7887) that was capable of efficient bioconversion of FR901459. Structural elucidation of the isolated bioconversion products (1-7) revealed that compounds 1-4 were mono-hydroxylated at the position of 1-MeBmt or 9-MeLeu, whereas compounds 5-7 were bis-hydroxylated at both positions. The results of morphological and chemical characterization, as well as phylogenetic analysis of 16S ribosomal DNA (rDNA), suggested that strain 7887 belonged to the genus Lentzea. Comparison of the FR901459 conversion activity of strain 7887 with several other Lentzea strains revealed that although all examined strains metabolized FR901459, strain 7887 had a characteristic profile with respect to bioconversion products. Taken together, these findings suggest that strain 7887 can be used to derivative FR901459 to produce a chemical template for further chemical modifications that may provide more effective and safer anti-HCV drugs.


Subject(s)
Actinobacteria/metabolism , Antiviral Agents/metabolism , Cyclosporine/metabolism , Immunosuppressive Agents/metabolism , Antiviral Agents/chemistry , Bacterial Typing Techniques , Biotransformation , Cluster Analysis , DNA, Bacterial/chemistry , DNA, Bacterial/genetics , DNA, Ribosomal/chemistry , DNA, Ribosomal/genetics , Hepacivirus/drug effects , Immunosuppressive Agents/chemistry , Magnetic Resonance Spectroscopy , Molecular Sequence Data , Molecular Structure , Phylogeny , RNA, Ribosomal, 16S/genetics , Sequence Analysis, DNA
3.
J Antibiot (Tokyo) ; 63(11): 643-7, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20924384

ABSTRACT

We screened actinomycetes capable of converting AS1387392 to AS1429716 and identified those strains capable of hydroxylation. Amycolatopsis azurea JCM 3275 was found to be a particularly efficient strain, capable of converting AS1387392 to AS1429716, with a yield of 44% after 9 h. This strain can metabolize not only the hydroxylation of phenylalanine at the meta and para positions but also the reduction of hydroxyketones, as shown by the isolation of bioconversion products. Examination of more suitable conversion conditions showed that pH 7.8 and 25 °C were the optimum pH and temperature for bioconversion, respectively. We also demonstrated the effect of carbon and nitrogen sources in the culture media on hydroxylation. Using this strain, we were able to efficiently produce AS1429716 as a chemical template. Further derivatization studies may provide more effective, safer immunosuppressants than those that are currently on-market.


Subject(s)
Actinomycetales/metabolism , Immunosuppressive Agents/metabolism , Peptides, Cyclic/metabolism , Carbon/chemistry , Culture Media/chemistry , Hydrogen-Ion Concentration , Hydroxylation , Nitrogen/chemistry , Temperature
4.
J Antibiot (Tokyo) ; 63(11): 649-56, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20924385

ABSTRACT

Biotransformation technology involving enzymatic modification of original substrates by organisms such as microbes is a valuable tool in improving pharmacokinetics or physicochemical properties of the base compounds. The fungal metabolite AS1387392 is a histone deacetylase inhibitor with potential as a therapeutic immunosuppressant. However, its paucity of functional groups, essential to synthesizing derivatives, is a drawback. Amycolatopsis azurea JCM-3275 catalyzed hydroxylation of AS1387392 to AS1429716, which may facilitate the synthesis of more derivatives by the additional hydroxyl moiety present in AS1429716. This reaction was inhibited by cytochrome P450 inhibitor metyrapone, indicating that cytochrome P450 may be responsible for the transformation. Degenerate PCR primers were subsequently constructed and used to clone genes encoding cytochrome P450 from the genomic DNA of A. azurea JCM-3275. We cloned an entire novel P450 gene (1209 bp) and named it P450Um-1. Its deduced amino acid sequence was homologous with that of the CYP105 subfamily. Further cloning of the upstream region, which may contain the native promoter site, was followed by insertion of the open reading frame with the upstream area into Streptomycetes high copy vector pIJ702, giving the expression plasmid pNUm-1. P450Um-1 was specifically expressed in Streptomyces lividans TK24, and this recombinant strain converted AS1387392 to AS1429716 without any redox partners. These results show that P450Um-1, a novel bacterial P450, catalyzed hydroxylation of AS1387392 to AS1429716. This resultant recombinant strain is expected to be an efficient biocatalyst with application to more suitable redox systems than those tested here.


Subject(s)
Actinomycetales/metabolism , Cytochrome P-450 Enzyme System/genetics , Immunosuppressive Agents/metabolism , Peptides, Cyclic/metabolism , Actinomycetales/enzymology , Amino Acid Sequence , Bacterial Proteins/genetics , Cloning, Molecular , Gene Expression Regulation, Enzymologic , Hydroxylation , Polymerase Chain Reaction/methods , Promoter Regions, Genetic , Streptomyces/genetics
5.
J Antibiot (Tokyo) ; 63(11): 637-42, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20664604

ABSTRACT

AS1387392 was a novel and powerful histone deacetylase inhibitor with an excellent oral absorption profile, but this compound was lacking in active moieties, which are essential to synthesize more derivatives. In our screening program to identify actinomycetes capable of converting AS1387392 to AS1429716, which has an active moiety to synthesize more derivatives, we identified 12 strains capable of efficient hydroxylation. Results of phylogenetic analysis of 16S rDNA sequences suggested that these strains belonged to the genera Lentzea, Saccharopolyspora, Sphaerisporangium and Amycolatopsis. Morphological and chemical characteristics as well as results of phylogenetic analysis suggested that strain No. 7980 was a new species belonging to the genus Amycolatopsis, according to the FASTA search result of 16S rDNA gene sequence. Using these strains, we can easily produce AS1429716 as a chemical template for further chemical modifications, which may provide more effective and safer immunosuppressant.


Subject(s)
Actinobacteria/metabolism , DNA, Ribosomal/chemistry , Immunosuppressive Agents/metabolism , Peptides, Cyclic/metabolism , Actinobacteria/genetics , Base Sequence , DNA, Bacterial/chemistry , Histone Deacetylase Inhibitors/metabolism , Phylogeny , Species Specificity
6.
J Antibiot (Tokyo) ; 63(11): 633-6, 2010 Nov.
Article in English | MEDLINE | ID: mdl-20588300

ABSTRACT

The novel immunosuppressant AS1387392 has been isolated from Acremonium sp. No. 27082. This compound showed a strong inhibitory effect against mammalian histone deacetylase and T-cell proliferation. Further, AS1387392 showed a good oral absorption, and its plasma concentration was higher than that of FR235222, an analog of AS1387392 that inhibited histone deacetylase previously reported. Given these findings, AS1387392 may represent an important new lead in developing immunosuppressant.


Subject(s)
Acremonium/chemistry , Histone Deacetylase Inhibitors/pharmacology , Histone Deacetylases/drug effects , Immunosuppressive Agents/pharmacology , Peptides, Cyclic/pharmacology , Animals , Cell Proliferation/drug effects , Female , Fermentation , Histone Deacetylase Inhibitors/isolation & purification , Histone Deacetylase Inhibitors/pharmacokinetics , Histone Deacetylases/metabolism , Humans , Immunosuppressive Agents/isolation & purification , Male , Mice , Mice, Inbred BALB C , Peptides, Cyclic/isolation & purification , Peptides, Cyclic/pharmacokinetics , Rats , Rats, Inbred Lew , T-Lymphocytes/drug effects , T-Lymphocytes/metabolism
7.
J Cardiovasc Pharmacol ; 43(5): 629-37, 2004 May.
Article in English | MEDLINE | ID: mdl-15071349

ABSTRACT

Effects of hypertension on the function of the Na+/Ca2+ exchanger (NCX) were investigated by analyzing vascular smooth muscle cells (VSMCs) from spontaneously hypertensive rats (SHR) and normotensive Wistar Kyoto (WKY) rats. Angiotensin II-induced 45Ca2+ efflux from VSMCs mediated by NCX was enhanced by up to 3-fold in SHR compared with WKY, whereas ionomycin-induced Ca efflux mediated by NCX was not different between SHR and WKY. The decline rate from the peak value of intracellular 45Ca2+ concentration ([Ca2+]i) mobilized by angiotensin II was decelerated by removal of extracellular sodium (Na+o) in SHR but not in WKY. Gene expressions of NCX subtype 1 and angiotensin II receptor type1A assessed by quantitative RT-PCR were increased by 1.3- and 1.5-fold, respectively in SHR compared with WKY. NCX protein was also increased 1.6-fold in SHR compared with WKY. MEK inhibitor, PD98059, partly blocked the Nao-dependent acceleration of the [Ca2+]i recovery rate and tyrosine kinase inhibitor, genistein, diminished it in SHR. Genistein decreased angiotensin II-induced Nao- dependent 45Ca2+ efflux. However, angiotensin II did not enhance the tyrosine phosphorylation of NCX. These results suggest that acceleration of Ca2+ efflux from VSMCs of SHR was at least partly due to the enhancement of functional activity of NCX via increased gene expression and tyrosine phosphorylation in connection with hypertension.


Subject(s)
Muscle, Smooth, Vascular/metabolism , Sodium-Calcium Exchanger/biosynthesis , Angiotensin II/pharmacology , Animals , Aorta/cytology , Calcium/metabolism , Cells, Cultured , Gene Expression , Genistein/pharmacology , Immunoblotting , Immunoprecipitation , Muscle, Smooth, Vascular/cytology , Phosphorylation , Protein Kinase Inhibitors/pharmacology , Rats , Rats, Inbred SHR , Rats, Inbred WKY , Receptor, Angiotensin, Type 1/biosynthesis , Receptor, Angiotensin, Type 1/genetics , Reverse Transcriptase Polymerase Chain Reaction , Sodium-Calcium Exchanger/genetics
8.
Jpn J Pharmacol ; 90(2): 164-72, 2002 Oct.
Article in English | MEDLINE | ID: mdl-12419887

ABSTRACT

The effect of antisense oligodeoxynucleotides (ODNs) of plasma membrane Ca(2+)-pumping ATPase (PMCA) on rat aortic vascular smooth muscle cells (VSMCs) in primary culture was examined. More than 80% of the PMCA expressed in cultured VSMCs was the PMCA-1B subtype. Exposed to antisense ODNs against PMCA-1, not only the expression of the PMCA protein but also mRNA of PMCA-1B was diminished in a concentration-dependent manner. Extracellular Na(+)-independent (45)Ca(2+) efflux catalyzed via PMCA was inhibited with antisense ODNs. Both the resting and ionomycin- or ATP-stimulated levels of intracellular Ca(2+) were increased by antisense ODNs. Furthermore, prolonged treatment with antisense ODNs caused apoptosis in VSMCs. The occurrence of apoptosis was inhibited by FK506, a potent immunosuppressant. These results demonstrate that the PMCA was specifically inhibited by antisense ODNs and suggest that PMCA plays an important role in regulation of intracellular Ca(2+) concentrations, especially at the resting condition to prevent an occurrence of apoptosis that may be induced through the activation of calcineurin.


Subject(s)
Apoptosis/drug effects , Calcium-Transporting ATPases/antagonists & inhibitors , Calcium-Transporting ATPases/physiology , Muscle, Smooth, Vascular/metabolism , Oligoribonucleotides, Antisense/pharmacology , Animals , Aorta/cytology , Apoptosis/physiology , Blotting, Western , Calcium/metabolism , Calcium-Transporting ATPases/biosynthesis , Cell Membrane/metabolism , Cells, Cultured , Flow Cytometry , Male , Muscle, Smooth, Vascular/cytology , Muscle, Smooth, Vascular/enzymology , Phosphorylation , RNA, Messenger/biosynthesis , Rats , Reverse Transcriptase Polymerase Chain Reaction
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