GLORIA

GEOMAR Library Ocean Research Information Access

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
Filter
  • 2005-2009  (9)
  • 1
    Publication Date: 2017-10-24
    Description: Copper, Cd and Zn can be found at elevated concentrations in contaminated estuarine and coastal waters and have potential toxic effects on phytoplankton species. In this study, the effects of these metals on the intracellular production of the polypeptides phytochelatin and glutathione by the marine diatom Phaeodactylum tricornutum were examined in laboratory cultures. Single additions of Cu and Cd (0.4 μM Cu2 and 0.45 μM Cd2+) to the culture medium induced the production of short-chained phytochelatins ((γ-Glu-Cys) n -Gly where n = 2-5), whereas a single addition of Zn (2.2 μM Zn2+) did not stimulate phytochelatin production. Combination of Zn with Cu resulted in a similar phytochelatin production compared with a single Cu addition. The simultaneous exposure to Zn and Cd led to an antagonistic effect on phytochelatin production, which was probably caused by metal competition for cellular binding sites. Glutathione concentrations were affected only upon exposure to Cd (85 increase) or the combination of Cd with Zn (65 decrease), relative to the control experiment. Ratios of phytochelatins to glutathione indicated a pronounced metal stress in response to exposures to Cu or Cd combined with Zn. This study indicates that variabilities in phytochelatin and glutathione production in the field can be explained in part by metal competition for cellular binding sites. © Springer 2006.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 2
    Publication Date: 2017-10-24
    Description: Phytochelatins (PCs) and glutathione (GSH) are -SH-containing compounds produced by a range of organisms for intracellular functions, such as protection against oxidative stress, metal detoxification and regulation of intracellular metal concentrations. These compounds, particularly PCs, have a potential use as metal-stress indicators for phytoplankton in natural waters. Despite their important roles, there is a paucity of data on intracellular GSH and PCs produced by natural phytoplankton assemblages. Current analytical methods for the determination of these compounds in phytoplankton from natural waters are based on high-performance liquid chromatography (HPLC) with detection of fluorescent derivatives, and comprise multi-step protocols. In this article, we discuss the analytical methods for HPLC determination of PCs and GSH, as there are limitations and practical challenges when they are applied to environmental studies. © 2005 Elsevier Ltd. All rights reserved.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 3
    Publication Date: 2020-07-20
    Description: Phytoplankton deal with metal toxicity using a variety of biochemical strategies. One of the strategies involves glutathione (GSH) and phytochelatins (PCs), which are metal-binding thiol peptides produced by eukaryotes and these compounds have been related to several intracellular functions, including metal detoxification, homeostasis, metal resistance and protection against oxidative stress. This paper assesses our state of knowledge on the production of PCs and GSH by marine phytoplankton in laboratory and field conditions and the possible applications of PCs for environmental purposes. Good relationships have been observed between metal exposure and PC production in phytoplankton in the laboratory with Cd, Pb, and Zn showing the greatest efficacy, thereby indicating that PCs have a potential for application as a biomarker. Fewer studies on PC distributions in particulate material have been undertaken in the field. These studies show that free Cu has a strong relationship with the levels of PC in the particulate material. The reason for this could be because Cu is a common contaminant in coastal waters. However it could also be due to the lack of measurements of other metals and their speciation. GSH shows a more complex relationship to metal levels both in the laboratory and in the field. This is most likely due to its multifunctionality. However, there is evidence that phytoplankton act as an important source of dissolved GSH in marine waters, which may form part of the strong organic ligands that control metal speciation, and hence metal toxicity. © 2006 by the Phycological Society of America.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 4
    Publication Date: 2017-10-24
    Description: Siderophores are chelates produced by bacteria as part of a highly specific iron uptake mechanism. They are thought to be important in the bacterial acquisition of iron in seawater and to influence iron biogeochemistry in the ocean. We have identified and quantified two types of siderophores in seawater samples collected from the Atlantic Ocean. These siderophores were identified as hydroxamate siderophores, both ferrioxamine species representative of the more soluble marine siderophores characterized to date. Ferrioxamine G was widely distributed in surface waters throughout the Atlantic Ocean, while ferrioxamine E had a more varied distribution. Total concentrations of the two siderophores were between 3 and 20 pM in the euphotic zone. If these compounds are fully complexed in seawater, they represent approximately 0.2-4.6 of the 〈0.2 μm iron pool. Our data confirm that siderophore-mediated iron acquisition is important for marine heterotrophic bacteria and indicate that siderophores play an important role in the oceanic biogeochemical cycling of iron. © 2008 American Chemical Society.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 5
    Publication Date: 2017-10-24
    Description: Four surveys of the Huelva Estuary in southwest Spain and its sources, the Tinto and the Odiel Rivers, were carried out between 1996 and 1998. The surveys investigated the impact of metalliferous mining of sulfide-rich ores in the catchment area on metal speciation, metal concentrations in a macrophyte, and phytoplankton diversity and abundance. Chemical speciation measurements in the lower Tinto Estuary showed that metals were predominantly electrochemically labile (>99 of total dissolved Cu, Co, and Ni at 10 μM Cu, 424 nM Co, and 500 nM Ni, S = 28). Concentrations of Cu complexing ligands and free cupric ions Cu2+ in the Gulf of Cádiz ranged between 5.3 and 38 nM and 0.2-7.9 pM, respectively, with conditional stability constants of the ligands of log K′CuL = 11.7-12.6. At enhanced dissolved Cu concentrations in the lower Huelva Estuary, Cu complexing ligands were saturated with Cu, resulting in nanomolar Cu2+, which increased upstream. Metal tissue concentrations of the macrophyte Blindingia marginata were high, and a clear relationship between dissolved labile Cu and macrophyte tissue Cu concentrations was observed. A low biodiversity was observed in the Huelva system (Shannon-Wiener indices (H) typically 〈0.2). Nevertheless, the maximum biomass was observed in the lower Tinto Estuary, which showed high labile metal and nutrient concentrations and a low biodiversity (H 〈 0.02), thereby suggesting adaptation through evolutionary processes of the phytoplankton community to the harsh conditions. © 2007 American Chemical Society.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 6
    Publication Date: 2017-10-24
    Description: The behaviour of a series of hydroxamate siderophores - microbially produced iron complexes - was investigated using electrospray ionisation mass spectrometry (ESI-MS). Three groups of iron hydroxamate siderophores, namely the ferrioxamines, ferrichromes and coprogens/ fusigens, were separated by high-performance liquid chromatography (HPLC) prior to ESI and MS2 fragmentation. For the majority of the siderophores, both protonated molecules and sodium adducts were observed. The most abundant ion was selected for collision-induced fragmentation. Potential fragmentation mechanisms are postulated and discussed. Fragmentation patterns differed between siderophore groups; however, common fragmentation patterns were observed for siderophore ions within the groups examined. Cleavage frequently occurred at carbon-nitrogen or carbon-oxygen bonds. Fragmentation of the ions also involved cleavage of iron-oxygen bonds and transfer of the charge to iron.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 7
    facet.materialart.
    Unknown
    Elsevier
    In:  Marine Chemistry, 103 (3-4). pp. 393-403.
    Publication Date: 2017-10-24
    Description: A method for the quantification of heme b in marine phyto- and bacterioplankton is described. Heme b was extracted from filtered cells using a solution of 2.5% octyl (3-glucopyranoside in 0.02 M ammonium hydroxide. The extract was analysed by high performance liquid chromatography diode array spectrophotometry. Maximum absorbance for heme b was at 400 nm. Heme b was separated from other pigments using a polystyrene divinyl benzene stationary phase and a gradient elution programme with 0.1% (v:v) nonafluoropentanoic acid in water and 50:50 (v:v) isopropanol:acetonitrile as the mobile phases. Heme b was quantified using Fe (III) protoporphyrin IX chloride (hemin) standards. The detection limit, calculated from 3 X s.d. of the lowest standard was 0.08 pmol or 1.57 nM with a 50 mu L injection volume. The first data for heme b in marine phyto- and bacterioplankton are reported. Heme b contents are reported for the eukaryotes Thalassiosira weissflogii, Thalassiosira oceanica, Dunaliella tertiolecta and Emiliania huxleyi, and the prokaryotes Synechococcus WH8102, WH7803, RCC307, Erythrobacter litoralis, Roseobacter denitrificans and Vibrio natriegens. For T. weissflogii, T. oceanica, D. tertiolecta and E. huxleyi cellular heme b concentrations varied between 12 and 60 mu mol L-1 and chlorophyll a to heme b ratios varied between 216 and 309
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 8
    Publication Date: 2017-10-24
    Description: Low molecular weight (LMW; 〈1 kDa) dissolved organic nitrogen ( DON) is the dominant DON fraction in marine systems. However, existing methods for DON characterization exclude this fraction through size exclusion or destruction during sample hydrolysis. In this study, we developed a method for the extraction and analysis of LMW peptides in saline waters. The procedure involves a solid phase extraction (SPE) preconcentration step using a polystyrene-divinylbenzene sorbent, then elution and detection by liquid chromatography-electrospray ionization-mass spectrometry (LC/ESI/MS). The procedure was tested with 1-L water samples containing peptides (10 ng L(-1)) ranging from 188.2-1946.0 Da. The analytes were characterized using "top-down" sequencing to confirm their structure, and the method was then successfully applied to saline water samples extracted from a mono-algal culture of Phaeodactylum tricornutum. This enabled a number of unknown analytes to be partially sequenced (complete sequencing should be possible using additional MS(n) scans and larger sample volumes). The method allows for the detection of peptides at the ng L(-1) level and further preconcentration is possible. The SPE step allowed determination of peptides from saline water, a matrix incompatible with direct LC/MS analysis. The method can, therefore, be used in DON characterization studies.
    Type: Article , PeerReviewed
    Format: text
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
  • 9
    facet.materialart.
    Unknown
    Royal Society of Chemistry
    In:  In: Metallothioneins and Related Chelators. , ed. by Sigel, A., Sigel, H. and Sigel, R. K. O. Royal Society of Chemistry, Cambridge, UK, pp. 441-482. ISBN 978-1-84755-899-2
    Publication Date: 2017-10-24
    Type: Book chapter , NonPeerReviewed
    Location Call Number Limitation Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...