Vladimir Zverlov

Dr. Vladimir Zverlov

orcid

Research Focus & Metrics

Academic Career Length

38Years (1989-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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22 September 2007 in Applied Microbiology and Biotechnology
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Journal Article
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DADominik Antoni
Dominik Antoni
VZVladimir Zverlov
Vladimir Zverlov
WSWolfgang H. Schwarz
Wolfgang H. Schwarz

10 May 2006 in Applied Microbiology and Biotechnology
Verified
Journal Article
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VZVladimir Zverlov
Vladimir Zverlov
OBO. Berezina
O. Berezina
GVG. A. Velikodvorskaya
G. A. Velikodvorskaya
WSW. H. Schwarz
W. H. Schwarz

1 October 2014 in Current Opinion in Biotechnology
Verified
Journal Article
Closed access
DKDaniela E Koeck
Daniela E Koeck
APAlexander Pechtl
Alexander Pechtl
VZVladimir Zverlov
Vladimir Zverlov
WSWolfgang H Schwarz
Wolfgang H Schwarz

11 August 2016 in Biotechnology for Biofuels
Verified
Journal Article
Open access
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IMIrena Maus
Irena Maus
DKDaniela E. Koeck
Daniela E. Koeck
KCKatharina G. Cibis
Katharina G. Cibis
SHSarah Hahnke
Sarah Hahnke
YKYong S. Kim
Yong S. Kim
MKMichael Klocke
Michael Klocke
One of the most promising technologies to sustainably produce energy and to mitigate greenhouse gas emissions from combustion of fossil energy carriers is the anaerobic digestion and biomethanation of organic raw material and waste towards biogas by highly diverse microbial consortia. In this context, the microbial systems ecology of thermophilic industrial-scale biogas plants is poorly understood. The microbial community structure of an exemplary thermophilic biogas plant was analyzed by a comprehensive approach comprising the analysis of the microbial metagenome and metatranscriptome complemented by the cultivation of hydrolytic and acido-/acetogenic Bacteria as well as methanogenic Archaea. Analysis of metagenome-derived 16S rRNA gene sequences revealed that the bacterial genera Defluviitoga (5.5 %), Halocella (3.5 %), Clostridium sensu stricto (1.9 %), Clostridium cluster III (1.5 %), and Tepidimicrobium (0.7 %) were most abundant. Among the Archaea, Methanoculleus (2.8 %) and Methanothermobacter (0.8 %) were predominant. As revealed by a metatranscriptomic 16S rRNA analysis, Defluviitoga (9.2 %), Clostridium cluster III (4.8 %), and Tepidanaerobacter (1.1 %) as well as Methanoculleus (5.7 %) mainly contributed to these sequence tags indicating their metabolic activity, whereas Hallocella (1.8 %), Tepidimicrobium (0.5 %), and Methanothermobacter (<0.1 %) were transcriptionally less active. By applying 11 different cultivation strategies, 52 taxonomically different microbial isolates representing the classes Clostridia, Bacilli, Thermotogae, Methanomicrobia and Methanobacteria were obtained. Genome analyses of isolates support the finding that, besides Clostridium thermocellum and Clostridium stercorarium, Defluviitoga tunisiensis participated in the hydrolysis of hemicellulose producing ethanol, acetate, and H2/CO2. The latter three metabolites are substrates for hydrogentrophic and acetoclastic archaeal methanogenesis. Obtained results showed that high abundance of microorganisms as deduced from metagenome analysis does not necessarily indicate high transcriptional or metabolic activity, and vice versa. Additionally, it appeared that the microbiome of the investigated thermophilic biogas plant comprised a huge number of up to now unknown and insufficiently characterized species.

2 March 2010 in Applied Microbiology and Biotechnology
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Journal Article
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OBOksana V. Berezina
Oksana V. Berezina
NZNatalia V Zakharova
Natalia V Zakharova
ABAgnieszka Brandt-Talbot
Agnieszka Brandt-Talbot
SYSergey V. Yarotsky
Sergey V. Yarotsky
WSWolfgang H. Schwarz
Wolfgang H. Schwarz
VZVladimir Zverlov
Vladimir Zverlov

15 March 2005 in Journal of Bacteriology
Verified
Journal Article
Open access
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VZVladimir Zverlov
Vladimir Zverlov
MKMichael Klein
Michael Klein
SLSebastian Lücker
Sebastian Lücker
MFMichael W. Friedrich
Michael W. Friedrich
JKJosef Kellermann
Josef Kellermann
MWMichael Wagner
Michael Wagner
In contrast to previous findings, we demonstrate that the dissimilatory (bi)sulfite reductase genes ( dsrAB ) of Desulfobacula toluolica were vertically inherited. Furthermore, Desulfobacterium anilini and strain mXyS1 were identified, by dsrAB sequencing of 17 reference strains, as members of the donor lineage for those gram-positive Desulfotomaculum species which laterally acquired dsrAB .