Conversion of 1-benzoylindole by Aspergillus strains

Applied Microbiology and Biotechnology

Volumn 53, Issue 6, 2000, Pages 695-700

  Sukhodolskaya, G V ^a   Nikolayeva, V M ^a   Donova, M V ^a   Gulevskaya, S A ^a   Baskunov, B P ^a   Koshcheyenko, K A ^a   Turchin, K F ^b  

^a SKRYABIN INSTITUTE OF BIOCHEMISTRY AND PHYSIOLOGY OF MICROORGANISMS   (Russian Federation)

^b Center for Drug Chemistry   (Russian Federation)

Author keywords

[No Author keywords available]

Indexed keywords

1 BENZOYLINDOLE; 4 HYDROXY 1 (4' HYDROXY) BENZOYLINDOLE; 4 HYDROXY 1 BENZOYLINDOLE; 4 HYDROXYINDOLE; 5 HYDROXYINDOLE; INDOLE; INDOLE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; ASPERGILLUS FLAVUS; ASPERGILLUS ORYZAE; BIOTRANSFORMATION; CONTROLLED STUDY; DRUG SYNTHESIS; HYDROXYLATION; MASS SPECTROMETRY; NONHUMAN; PROTON NUCLEAR MAGNETIC RESONANCE; STRUCTURE ANALYSIS; THIN LAYER CHROMATOGRAPHY;

ASPERGILLUS; ASPERGILLUS FLAVUS; ASPERGILLUS ORYZAE;

EID: 0033935604     PISSN: 01757598     EISSN: None     Source Type: Journal    
DOI: 10.1007/s002530000317     Document Type: Article

References (31)

1. Allen CCR, Boyd DR, Larkin MJ, Reid KA, Sharma ND, Wilson K (1997) Metabolism of naphthalene, 1-naphthol, indene, and indole by Rhodococcus sp. Strain Neimb-12038. Appl Environ Microbiol 63: 151-155
2. Baklashova TG, Koshcheyenko KA, Skryabin GK (1984) Hydroxylation of indolyl-3-acetic acid by immobilised mycelium of Aspergillus niger. Appl Microbiol Biotechnol 19: 217-230
3. Baklashova TG, Koshcheyenko KA, Sokolova EN (1990) Hydroxylation of indolyl-3-acetic acid by Aspergillus niger VKM F-212 immobilised in Ca-alginate gel and carrageenan. Prikl Biochim Mikrobiol 26: 26-32 (in Russian)
4. Berry DF, Madsen EL, Bollag JM (1987) Conversion of indole to oxindole under methanogenic conditions. Appl Environ Microbiol 53: 180-182
5. Black PT, Hefferman ML (1965) The analysis of the proton magnetic resonance spectra of heteroaromatic systems. IV. Benzofuran, indole and related compounds. J Chem 3: 353-357
6. Cho SH, Andersen JA (1982) 5-Hydroxytryptophan and soluble pigment formation in Claviceps sp. PRL. Phytochemistry 21: 1975-1976
7. Dodge RH, Cerniglia CE, Gibson DT (1979) Fungal metabolism of biphenyl. Biochem J 178: 223-230
8. Duran N, Antonio RV, Haun M, Pilli RA (1994) Biosynthesis of trypanocide by Chromobacterium violaceum. World J Microbiol Biotechnol 10: 686-690
9. Dvornikova TP (1980) Microbiological synthesis and conversion of indole compounds (in Russian). Shtiinza, Kishinev
10. Ensley BD, Ratzkin BJ, Osslund TD, Simon MJ, Wackett LP, Gibson DT (1983) Expression of naphthalene oxidation genes in Escherichia coli results in the biosynthesis of indigo. Science 222: 167-169
11. Ezhov VA, Trushkina AG, Koslovskii AG (1993) A method for isolating 4- and/or 5- hydroxyindole-3-acetic acid. SU Patent 1822885
12. Fujioka MH, Wada H (1968) The bacterial oxidation of indole. Biochim Biophys Acta 158: 70-78
13. Gibson DT, Subramanian V (1984) Microbial degradation of aromatic hydrocarbons. In: Gibson DT (ed) Microbial degradation of aromatic compounds. Dekker, New York, pp 181-252
14. Gordon A, Ford R (1976) Sputnik khimika (in Russian). Mir, Moscow
15. Gu JD, Berry DF (1992) Metabolism of 3-methylindole by a methanogenic consortium. Appl Environ Microbiol 58: 2667-2669
16. Gupta A, Rao K (1977) Role of biotin in ergot alkaloid formation by Aspergillus fumigatus. Indian J Biochem Biophys 14: 84-85
17. Jochen G (1990) Verfahren zur Gewinnung von Tryptophanderivaten durch Kultivierung höherer Pilze. De Patent 278600
18. Kamath AV, Vaidyanathan CS (1990) New pathway for the biodegradation of indole in Aspergillus niger. Appl Environ Microbiol 56: 275-280
19. Madsen EL, Bollag JM (1987) Pathway of indole metabolism by nitrifying microbial community. Arch Microbiol 151: 71-76
20. Martin R, Junino A (1994) Preparation of indole or indoline pigment by oxidation of indole or indoline derivative. Fr Patent 2694021
21. Memoli S, Napolitano A, Dishia M, Misuraca G, Palumbo A, Prota G (1997) Diffusible melanin-related metabolites are potent inhibitors of lipid peroxidation. Biochem Biophys Acta 1346: 61-68
22. Mimura A, Takahashi Y, Yasuyki K, Shibukawa M (1982) Process for producing L-tryptophan or derivatives thereof using a microorganism. US Patent 4349627
23. Muncnerova D, Agustin J (1994) Fungal metabolism and detoxification of polycyclic aromatic hydrocarbons. Bioresour Technol 48: 97-106
24. NSDC (1974) Eight peak index of mass spectra, vol 2, table 2, 2nd edn. AWRE, Aldemaston
25. O'Connor KE, Dobson ADV, Hartmans S (1997) Indigo formation by microorganisms expression styrene monooxygenase activity. Appl Environ Microbiol 63: 4287-4291
26. Ryabova SYU, Granik VG (1995) Advances in indoxyl chemistry (in Russian). Khim Farm Zh 29: 3-22
27. Shcherbakova VA, Obraztsova AYa, Laurinavichyus KS, Akimenko VK (1997) Transformation of indoles by pure and accumulative cultures of methane producing bacteria (in Russian). Prikl Biochim Mikrobiol 33: 75-79
28. Subramanian V, Sugumaran M, Vaidyanathan CS (1978) Double hydroxylation reaction in microorganisms. J Indian Inst Sci 60: 143-178
29. Tuloup R, Lagrange A, Philippe M (1997) Process for the preparation of indole compounds. EP Patent 776977
30. Yajima Y (1987) Production of tryptophan or derivatives. JP Patent 62205791
31. Yuzhakov SV (1995) Actual problems of the search and creating of adrenoblockators. Khim Farm Zh 29: 3-5 (in Russian)