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Dive into the research topics where M. U. Arinbasarov is active.

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Featured researches published by M. U. Arinbasarov.


Applied Biochemistry and Microbiology | 2005

Production of mycophenolic acid by fungi of the genus Penicillium link

N. G. Vinokurova; N. E. Ivanushkina; G. A. Kochkina; M. U. Arinbasarov; S. M. Ozerskaya

Out of 36 strains of fungi of the genus Penicillium, some of which were isolated from ancient permafrost, 14 strains synthesized mycophenolic acid (MPA). Maximal (over 500 mg/l) accumulation of MPA in culture liquid was observed in P. brevicompactum strains (VKM F-457, VKM F-477, and VKM F-1150). This was the first study to detect MPA in representatives of the species P. rugulosum; in three strains of this species (VKM FW-665, VKM FW-717, and VKM FW-733), the level of MPA accumulation exceeded 300 mg/l. The time course of the synthesis of MPA by P. rugulosum strain VKM FW-733 was studied. It was shown that the synthesis of this metabolite was dramatically intensified during the stationary growth phase (ten days).


Applied Biochemistry and Microbiology | 2007

Synthesis of α-cyclopiazonic acid by fungi of the genus Aspergillus

N. G. Vinokurova; N. E. Ivanushkina; I. I. Khmel’nitskaya; M. U. Arinbasarov

The presence of α-cyclopiazonic acid has been studied among metabolites of Aspergillus fungi. The study was performed with 138 cultures of 13 species obtained from the All-Russia Collection of Microorganisms and the collection of our institute. α-Cyclopiazonic acid was most frequently encountered among the metabolites of the section Flavi (the ability to synthesize α-cyclopiazonic acid was expressed in 61% of the strains of A. flavus, 83% of the strains of A. oryzae, and all strains of A. tamarii). This expression index for A. versicolor was less than 5%. We showed for the first time that α-cyclopiazonic acid is produced by A. fumigatus and A. phoenicis (expression in 30% of the strains of either species).


Microbiology | 2003

The Penicillium commune Thom and Penicillium clavigerum Demelius Fungi Producing Fumigaclavines A and B

N. G. Vinokurova; S. M. Ozerskaya; B. P. Baskunov; M. U. Arinbasarov

The type strains Penicillium clavigerum VKM F-447 and P. commune VKM F-3233 are found to produce fumigaclavines A and B. Of the seven other strains of these species, only two strains, P. commune VKM F-3088 and F-3491, possess the ability to synthesize these alkaloids. It is suggested that the five other strains under study either lost such an ability or require very specific conditions for the synthesis of these alkaloids.


Applied Biochemistry and Microbiology | 2003

Production of Alkaloids by Fungi of the Genus PenicilliumGrown on Wheat Grain

N. G. Vinokurova; L. V. Boichenko; M. U. Arinbasarov

The ability to produce alkaloids has been studied in 13 strains belonging to ten species of the genus Penicillium. Most of these strains produce identical ranges of alkaloids when grown on wheat grain and synthetic Abes medium. These are roquefortine, 3,12-dihydroroquefortine, and glandicolines A and B in strain P. chrysogenum VKM F-1987; fumigaclavines A and B, festuclavine, and pyroclavine in P. commune VKM F-308, F-3491, and KBP4; agroclavine 1 and epoxyagroclavine 1 in P. fellutanum VKM F-1073; fellutanine A in P. fellutanum F-3020; roquefortine, 3,12-dihydroroquefortine, meleagrin, and glandicolines A and B in P. glandicola VKM F-743; aurantioclavine in P. nalgiovense VKM F-229; isofumigaclavines A and B, festuclavine, roquefortine, and 3,12-dihydroroquefortine in P. roquefortii VKM F-2389; roquefortine, 3,12-dihydroroquefortine, and meleagrin in P. vitale VKM F-3624; roquefortine and oxaline in P. vulpinum VKM F-256; and α-cyclopiazonic acid and rugulovasine B in P. viridicatum C-47. No alkaloids were found in P. rugulosum VKM F-352 grown on wheat grain. A simple method is proposed for isolating alkaloids from affected grain.


Applied Biochemistry and Microbiology | 2001

Biodegradation of Oil Products by Individual Degrading Strains and Their Associations in Liquid Media

L. M. Baryshnikova; V. G. Grishchenkov; M. U. Arinbasarov; A. N. Shkidchenko; L. M. Boronin

The degrading activities of selected bacterial strains and their associations directed towards fuel oil and diesel fuel in liquid media were studied. Two-member associations composed preferably by RhodococcusandPseudomonasstrains demonstrated the highest degrading efficiencies. No enhancement was achieved when the number of association members was increased to three, four, or five strains. The population stability of any member strain was found to depend on the association composition.


Applied Biochemistry and Microbiology | 2003

Analysis of secondary metabolites of microscopic fungi of the genus Penicillium by chromatographic techniques

N. F. Zelenkova; N. G. Vinokurova; M. U. Arinbasarov

Combinations of various systems of thin-layer chromatography and high-performance liquid chromatography (HPLC) were efficient in analyzing 39 nitrogen-containing secondary metabolites (alkaloids) produced by 12 strains of microscopic fungi of the genus Penicillium. Chromatographic mobility of alkaloids on Silufol plates was determined in the following systems: (a) chloroform, methanol, and 25% NH4OH (90 : 10 : 1, 90 : 10 : 0.1, or 80 : 20 : 0.2); (b) chloroform and acetone (9 : 1); and (c) ethyl acetate, methanol, and 25% NH4OH (85 : 15 : 10); staining was performed using Ehrlichs reagent. Conditions for separation of clavine alkaloids by HPLC on Spherisorb ODS-2 and Supelcosil LC-18 columns (gradient elution) were optimized. Retention values of 22 alkaloids were compared to those of agroclavine and roquefortine.


Microbiology | 2001

Screening for Ergot Alkaloid Producers among Microscopic Fungi by Means of the Polymerase Chain Reaction

L. V. Boichenko; D. M. Boichenko; N. G. Vinokurova; T. A. Reshetilova; M. U. Arinbasarov

The potential of the polymerase chain reaction for the detection of ergot alkaloid producers among microscopic fungi of the generaPenicilliumand Clavicepswas evaluated. Twenty-three strains of various species of fungi with a previously studied capacity for alkaloid production were used. The internal fragment of the gene encoding 4-dimethylallyltryptophan synthase, the enzyme catalyzing the first step in the biosynthesis of ergot alkaloids, was amplified using degenerate primers. This approach revealed an about 1.2-kb specific DNA fragment in micromycetes synthesizing ergot alkaloids with complete tetracyclic ergoline system. Microorganisms that produce alkaloids with modified C or D ergoline rings, as well as α-cyclopiazonic acid, did not yield the PCR fragment of the expected size. This fragment was also not found in fungi incapable of ergot alkaloid production.


Applied Biochemistry and Microbiology | 2001

Minor Alkaloids of the Fungus Penicillium roquefortiiThom 1906

N. G. Vinokurova; D. M. Boichenko; B. P. Baskunov; N. F. Zelenkova; I. G. Vepritskaya; M. U. Arinbasarov; T. A. Reshetilova

New isomers of clavine alkaloids with distinctively low chromatographic mobilities were isolated from the collection and mutant strains of Penicillium roquefortiiThom 1906, in addition to alkaloids roquefortine, 3,12-dihydroroquefortine, isofumigaclavines A and B, festuclavine, and chanoclavine-I, which are characteristic of this species. It was demonstrated that the collection strain produces isomers of agroclavine and epoxyagroclavine, whereas the mutant strain synthesizes isomers of fumigaclavines A and B, festuclavine, and chanoclavine.


Applied Biochemistry and Microbiology | 2003

Occurrence of Indole Alkaloids among Secondary Metabolites of Soil Aspergillus Spp.

N. G. Vinokurova; I. I. Khmel'nitskaya; B. P. Baskunov; M. U. Arinbasarov

The occurrence of indole alkaloids among secondary fungal metabolites was studied in species of the genus Aspergillus, isolated from soils that were sampled in various regions of Russia (a total of 102 isolates of the species A. niger, A. phoenicis, A. fumigatus, A. flavus, A. versicolor, A. ustus, A. clavatus, and A. ochraceus). Clavine alkaloids were represented by fumigaclavine B, which was formed by A. fumigatus. α-Cyclopiazonic acid was formed by isolates of A. fumigatus, A. flavus, A. versicolor, A. phoenicis, and A. clavatus. The occurrence of indole-containing diketopiperazine alkaloids was documented for isolates of A. flavus, A. fumigatus, A. clavatus, and A. ochraceus. No indole-containing metabolites were found among the metabolites of A. ustus or A. niger.


Microbiology | 2007

Effect of catabolic plasmids on physiological parameters and efficiency of oil destruction by Pseudomonas bacteria

A. A. Vetrova; I. A. Nechaeva; Ignatova Aa; I. F. Puntus; M. U. Arinbasarov; A. E. Filonov; A. M. Boronin

The ability of microbial degraders of polycyclic aromatic hydrocarbons to grow at 24°C in liquid mineral medium supplemented with oil as the sole source of carbon and energy was studied. Growth characteristics (CFU) and the level of oil destruction by plasmid-bearing and plasmid-free strains were determined after seven days of cultivation. The presence of catabolic plasmids in the degrader strains, including rhizosphere pseudomonads, was shown to increase cell growth and enhance the level of oil degradation. Strain Pseudomonas chlororaphis BS1391 bearing plasmid pBS216 was found to be the most effective oil degrader.

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N. G. Vinokurova

Russian Academy of Sciences

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N. F. Zelenkova

Russian Academy of Sciences

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B. P. Baskunov

Russian Academy of Sciences

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T. A. Reshetilova

Russian Academy of Sciences

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L. V. Boichenko

Russian Academy of Sciences

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A. M. Boronin

Russian Academy of Sciences

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D. M. Boichenko

Russian Academy of Sciences

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A. N. Shkidchenko

Russian Academy of Sciences

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V. G. Grishchenkov

Russian Academy of Sciences

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A. A. Vetrova

Russian Academy of Sciences

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