Microorganisms of low-temperature heavy oil reservoirs (Russia) and their possible application for enhanced oil recovery


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Abstract

Physicochemical and microbiological characteristics of formation waters low-temperature heavy oil reservoirs (Russia) were investigated. The Chernoozerskoe, Yuzhno-Suncheleevskoe, and Severo-Bogemskoe oilfields, which were exploited without water-flooding, were shown to harbor scant microbial communities, while microbial numbers in the water-flooded strata of the Vostochno-Anzirskoe and Cheremukhovskoe oilfields was as high as 106 cells/mL. The rates of sulfate reduction and methanogenesis were low, not exceeding 1982 ng S2–/(L day) and 9045 nL СН4/(L day), respectively, in the samples from water-flooded strata. High-throughput sequencing of microbial 16S rRNA gene fragments in the community of injection water revealed the sequences of the Proteobacteria (74.7%), including Betaproteobacteria (40.2%), Alphaproteobacteria (20.7%), Gammaproteobacteria (10.1%), Deltaproteobacteria (2.0%), and Epsilonproteobacteria (1.6%), as well as Firmicutes (7.9%), Bacteroidetes (4.1%), and Archaea (0.2%). DGGE analysis of microbial mcrA genes in the community of injection water revealed methanogens of the genera Methanothrix, Methanospirillum, Methanobacterium, Methanoregula, Methanosarcina, and Methanoculleus, as well as unidentified Thermoplasmata. Pure cultures of bacteria of the genera Rhodococcus, Pseudomonas, Gordonia, Cellulomonas, etc., capable of biosurfactant production when grown on heavy oil, were isolated. Enrichment cultures of fermentative bacteria producing significant amounts of volatile organic acids (acetic, propionic, and butyric) from sacchariferous substrates were obtained. These acids dissolve the carbonates of oil-bearing rock efficiently. Selection of the efficient microbial technology for enhanced recovery of heavy oil from terrigenous and carbonate strata requires model experiments with microbial isolates and the cores of oil-bearing rocks.

About the authors

T. N. Nazina

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Author for correspondence.
Email: nazina@inmi.ru
Russian Federation, Moscow

D. Sh. Sokolova

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

T. L. Babich

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

E. M. Semenova

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

A. P. Ershov

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

S. Kh. Bidzhieva

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

I. A. Borzenkov

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

A. B. Poltaraus

Engelhardt Institute of Molecular Biology

Email: nazina@inmi.ru
Russian Federation, Moscow

M. R. Khisametdinov

Tatar Oil Research and Design Institute (TatNIPIneft)

Email: nazina@inmi.ru
Russian Federation, Bugulma

T. P. Tourova

Winogradsky Institute of Microbiology, Research Center of Biotechnology

Email: nazina@inmi.ru
Russian Federation, Moscow

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