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Worldwide plastic production has surged over the past 50 years. In 2016, it reached 335 million tonnes per annum, with Europe alone producing 60 million tonnes. Over the next 20 years, it is expected to double. Plastic packaging is the most important product (26% of the total volume of all plastics used), although it has a short life compared to plastics used in, for example, the construction and car industries. Plastic producers and transformers are keen to highlight the benefits derived from plastic packaging; not only does it deliver direct economic profits, but it also helps prevent food waste and contamination. Further, by lessening the weight of packaging, it can reduce the fuel used in the transport of goods. This is certainly important, but even if these plastics are re-used, they inevitably become waste at some point. If we are to close the loop of the circular economy, this waste needs to be seen as a resource to be plugged back into the life cycle of plastics (PlasticsEurope, 2018). [ABSTRACT FROM AUTHOR]

Organic wastes are a suitable feedstock for the production of value-added products that have been insufficiently exploited due to their complexity, which challenges their transformation by conventional procedures. Gasification and pyrolysis of organic wastes can reduce this complexity by producing syngas ( CO plus H2 and other C1 gases), which can be used as a valuable commodity by catalytic conversion into chemicals. However, the high cost and susceptibility to poisoning of chemical catalysts have encouraged research on biocatalysts that convert C1 components of syngas into different multi-carbon compounds. Nowadays, research on syngas fermentation is receiving much attention in order to enhance the productivity of microorganisms by remodeling their metabolism and by optimizing the bioreactor operational conditions. This review highlights the new technical achievements of pyrolysis as well as the new biotechnological uses of syngas for the production of bulk chemicals and biopolymers, discussing the major bottlenecks that challenge syngas fermentation. © 2015 Society of Chemical Industry [ABSTRACT FROM AUTHOR]

This review about the genus Gordonia provides a current overview of recent research on a young genus that was introduced in the year 1997 (Stackebrandt et al., 1997). This emerging genus has attracted increasing environmental, industrial, biotechnological and medical interest during the last few years, in particular due to the capabilities of its members to degrade, transform, and synthesize organic compounds as well as to the pathogenic effects that have been described in many case studies. The number of publications about Gordonia has increased significantly after the year 2004 (the year of the first Gordonia review published by Arenskötter et al.) describing 13 new validly published species (type strains), many newly described physiological and metabolic capabilities, new patent applications and many new case reports of bacterial infections. Members of the genus Gordonia are widely distributed in nature and it is therefore important to unravel the species richness and metabolic potential of gordoniae in future studies to demonstrate their environmental impact especially on the degradation of persistent organic compounds and their ecological participation in the carbon cycle of organic material in soil and water. This review summarizes mainly the current state of importance and potential of the members of this genus for the environmental and biotechnological industry ('the strengthsâ) and briefly its pathogenic impact to humans ('the weaknessesâ). [ABSTRACT FROM AUTHOR]

The aerobic degradation of cholesterol, testosterone, androsterone, progesterone, and further steroid compounds as sole carbon source has been observed in the newly isolated bacterial Gram-positive strain Chol-4. The 16S rRNA gene sequence shares the greatest similarity with members of the genus Rhodococcus, with the closest shared nucleotide identities of 98–99% with Rhodococcus ruber (DSM 43338T) and Rhodococcus aetherivorans (DSM 44752T). Phylogenetic analysis of Rhodococcus 16S rRNA gene sequences consistently places strain Chol-4 in a clade shared with those both type strains within the Rhodococcus rhodochrous subclade. The results of DNA–DNA hybridization against its two phylogenetically closest neighbors as well as the results of morphological, physiological, and biochemical tests allowed genotypic and phenotypic differentiation of strain Chol-4 from Rhodococcus ruber (DSM 43338T) on the species level and from the other validly described Rhodococcus species on the genus level. Strain Chol-4 therefore merits recognition as a novel strain of the species Rhodococcus ruber and demonstrates for the first time the capability of this species to utilize a great variety of steroid compounds as growth substrates never shown for other species of this genus so far. The genome of strain Chol-4 harbors at least one gene cluster that may be responsible for the degradation of steroid compounds. This gene cluster was identified in a cloned 5458 bp BamHI– EcoRV DNA fragment and compared to similar genes from other Gram-positive and Gram-negative bacteria described so far. [ABSTRACT FROM AUTHOR]

Examines the dehalogenation of chlorinated ethenes and immobilization of nickel in anaerobic sediment columns under sulfidogenic condition. Decrease in nickel concentration; Effects of microbial activity on the precipitation of heavy metals; Role of negative reduction-oxygenation activity of sulfate-reducing bacteria on the activity of dehalogenating bacteria.

Examines the tetrachloroethene (PCE) dehalorespiration and growth of sulfate-reducing bacterium Desulfovibrio fructosivorans and Desulfitobacterium frappieri. Use of fructose as single electron donor; Domination of the sulfate reduction process; Dehalogenation of PCE by a dehalorespiring anaerobe.

Provides information on a series of experiments conducted to evaluate the level of incorporation of ...C-labeled 2,4,6-trinitrotoluene (TNT) and metabolites into the organic soil matrix of anaerobic and sequential anaerobic-aerobic treated soil/molasses mixtures. Materials and methods; Results; Discussion.

Investigations were carried out to evaluate the level of incorporation of radiolabeled 2,4,6-trinitrotoluene (TNT) and metabolites into the bacterial biomass of two different bacterial species after cometabolically mediated TNT transformation. Biotransformation experiments with 14C-TNT indicated that TNT was not mineralized; however, carbon derived from TNT became associated with the cells. It was found that more than 42% of the initially applied radiolabel was associated with the cell biomass after cometabolic 14C-TNT transformation with the strictly anerobic Desulfovibrio species strain SHV, whereas with the strictly aerobic Serratia plymuthica species strain B7, 32% of cell-associated 14C activity was measured. The remainder of the radiolabel was present in the supernatants of the liquid cultures in the form of different TNT metabolites. Under anoxic conditions with the Desulfovibrio species, TNT was ultimately transformed to 2,4,6-triaminotoluene (TAT) and both diaminonitrotoluene isomers, whereas under oxic conditions with the Serratia species, TNT was converted to hydroxylaminodinitrotoluenes and aminodinitrotoluenes, with 4-amino-2,6-dinitrotoluene (4ADNT) being the major end product. In both culture supernatants, small amounts of very polar, radiolabeled, but unidentified metabolites were detected. At the end of the experiments approximately 92% and 96% of the originally applied radioactivity was recovered in the studies with the Serratia and Desulfovibrio species, respectively. [ABSTRACT FROM AUTHOR]

The taxonomic position of the cholesterol-degrading strain Chol-3(T), isolated from a sewage sludge sample, was clarified using a polyphasic taxonomic approach. Phylogenetic analysis of its 16S rRNA gene sequence, whole-cell fatty acid profile and mycolic acid composition revealed that this isolate is a member of the genus Gordonia with the species Gordonia sihwensis, G. hydrophobica and G. shandongensis being the nearest phylogenetic neighbours. The results of DNA-DNA hybridization against its phylogenetically closest neighbours as well as the results of physiological and biochemical tests allowed genotypic and phenotypic differentiation of strain Chol-3(T) from the other Gordonia species with validly published names. Strain Chol-3(T) therefore merits recognition as a member of a novel species within the genus Gordonia, for which the name Gordonia cholesterolivorans sp. nov. is proposed. The type strain is Chol-3(T) (=CECT 7408(T) =DSM 45229(T)).

Sulfate-reducing bacteria (SRB) from termites have been assigned to the genus Desulfovibrio. Desulfovibrio intestinalis lives in the gut of the Australian termite Mastotermes darwiniensis. For the first time we were able to enrich and identify a sulfate-reducing bacterium from the gut of the rose-chafer Pachnoda marginata, which showed the highest 16S rDNA sequence identity (93%) to Desulfovibrio intestinalis and Desulfovibrio strain STL1. Compared to Mastotermes darwiniensis (1x10(7) cells of SRB per ml gut contents), sulfate-reducing bacteria occurred in higher numbers in the gut contents of Pachnoda marginata reaching cell titers of up to 2x10(8) cells per ml gut contents. In vitro sulfate reduction rates were determined with SRB from the gut contents of the termite Mastotermes darwiniensis and the beetle Pachnoda marginata. Due to the higher cell titer, the sulfate reduction rate of Pachnoda marginata was 10(4) nmolxh-1xml-1 and therefore, 21 times higher than that of Mastotermes darwiniensis. In addition, we detected in vivo sulfate reduction in Mastotermes darwiniensis, which indicates that sulfate reducers play an active role in the sulfur metabolism in the termite gut.