26 research outputs found
Knockout of the folate transporter folt-1 causes germline and somatic defects in C. elegans
<p>Abstract</p> <p>Background</p> <p>The <it>C. elegans </it>gene <it>folt-1 </it>is an ortholog of the human reduced folate carrier gene. The FOLT-1 protein has been shown to transport folate and to be involved in uptake of exogenous folate by worms. A knockout mutation of the gene, <it>folt-1(ok1460)</it>, was shown to cause sterility, and here we investigate the source of the sterility and the effect of the <it>folt-1 </it>knockout on somatic function.</p> <p>Results</p> <p>Our results show that <it>folt-1(ok1460) </it>knockout hermaphrodites have a substantially reduced germline, generate a small number of functional sperm, and only rarely produce a functional oocyte. We found no evidence of increased apoptosis in the germline of <it>folt-1 </it>knockout mutants, suggesting that germline proliferation is defective. While <it>folt-1 </it>knockout males are fertile, their rate of spermatogenesis was severely diminished, and the males were very poor maters. The mating defect is likely due to compromised metabolism and/or other somatic functions, as <it>folt-1 </it>knockout hermaphrodites displayed a shortened lifespan and elongated defecation intervals.</p> <p>Conclusions</p> <p>The FOLT-1 protein function affects both the soma and the germline. <it>folt-1(ok1460) </it>hermaphrodites suffer severely diminished lifespan and germline defects that result in sterility. Germline defects associated with folate deficiency appear widespread in animals, being found in humans, mice, fruit flies, and here, nematodes.</p
Biofilm Engineering Approaches for Improving the Performance of Microbial Fuel Cells and Bioelectrochemical Systems
Microbial fuel cells (MFCs) are emerging as a promising future technology for a wide range of applications in addition to sustainable electricity generation. Electroactive (EA) biofilms produced by microorganisms are the key players in the bioelectrochemical systems involving microorganism mediated electrocatalytic reactions. Therefore, genetically modifying the organism for increased production of EA biofilms and improving the extra electron transfer (EET) mechanisms may attribute to increase in current density of a MFC and an increased COD removal in wastewater treatment plant coupled MFC systems. Extracellular polysaccharides (EPS) produced by the organisms attribute to both biofilm formation and electron transfer. Although cell surface modification, media optimization and operation parameters validation are established as enhancement strategies for a fuel cell performance, engineering the vital genes involved in electroactive biofilm formation is the future hope. Therefore, in this review we critically address the biofilm formation mechanisms in electro active microorganisms, strategies for improving the biofilm formation leading to improved electrocatalytic rates for applications in bioelectrochemical systems
Clinical, pathological and functional characterization of riboflavin-responsive neuropathy.
Brown-Vialetto-Van Laere syndrome represents a phenotypic spectrum of motor, sensory, and cranial nerve neuropathy, often with ataxia, optic atrophy and respiratory problems leading to ventilator-dependence. Loss-of-function mutations in two riboflavin transporter genes, SLC52A2 and SLC52A3, have recently been linked to Brown-Vialetto-Van Laere syndrome. However, the genetic frequency, neuropathology and downstream consequences of riboflavin transporter mutations are unclear. By screening a large cohort of 132 patients with early-onset severe sensory, motor and cranial nerve neuropathy we confirmed the strong genetic link between riboflavin transporter mutations and Brown-Vialetto-Van Laere syndrome, identifying 22 pathogenic mutations in SLC52A2 and SLC52A3, 14 of which were novel. Brain and spinal cord neuropathological examination of two cases with SLC52A3 mutations showed classical symmetrical brainstem lesions resembling pathology seen in mitochondrial disease, including severe neuronal loss in the lower cranial nerve nuclei, anterior horns and corresponding nerves, atrophy of the spinothalamic and spinocerebellar tracts and posterior column-medial lemniscus pathways. Mitochondrial dysfunction has previously been implicated in an array of neurodegenerative disorders. Since riboflavin metabolites are critical components of the mitochondrial electron transport chain, we hypothesized that reduced riboflavin transport would result in impaired mitochondrial activity, and confirmed this using in vitro and in vivo models. Electron transport chain complex I and complex II activity were decreased in SLC52A2 patient fibroblasts, while global knockdown of the single Drosophila melanogaster riboflavin transporter homologue revealed reduced levels of riboflavin, downstream metabolites, and electron transport chain complex I activity. This in turn led to abnormal mitochondrial membrane potential, respiratory chain activity and morphology. Riboflavin transporter knockdown in Drosophila also resulted in severely impaired locomotor activity and reduced lifespan, mirroring patient pathology, and these phenotypes could be partially rescued using a novel esterified derivative of riboflavin. Our findings expand the genetic, clinical and neuropathological features of Brown-Vialetto-Van Laere syndrome, implicate mitochondrial dysfunction as a downstream consequence of riboflavin transporter gene defects, and validate riboflavin esters as a potential therapeutic strategy
β-fructofuranosidase production by 2-deoxyglucose resistant mutants of <i><span style="font-size:14.0pt;line-height:115%;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";color:black;mso-ansi-language:EN-IN; mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN">Aspergillus niger </span></i><span style="font-size:14.0pt;line-height:115%;font-family:"Times New Roman"; mso-fareast-font-family:"Times New Roman";color:black;mso-ansi-language:EN-IN; mso-fareast-language:EN-IN;mso-bidi-language:HI" lang="EN-IN">in submerged and solid-state fermentation</span>
1032-1037<span style="font-size:14.0pt;line-height:
115%;font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN">Aspergillus niger
<span style="font-size:14.0pt;line-height:115%;
font-family:" times="" new="" roman";mso-fareast-font-family:"times="" roman";="" color:black;mso-ansi-language:en-in;mso-fareast-language:en-in;mso-bidi-language:="" hi"="" lang="EN-IN">produces extracellular β-fructofuranosidase under submerged (SmF) and solid
state fermentation(SSF) conditions. After UV mutagenesis of conidiospores of A.
<i style="mso-bidi-font-style:
normal">niger,
2-deoxyglucose (10 g/l) resistant mutants were isolated on Czapek's minimal
medium containing glycerol as a carbon source and the mutants were examined for
improved production of β-fructofuranosidase in SmF and SSF conditions. One of
such mutant DGRA-1 overproduced β-fructofuanosidase in both SmF and SSF
conditions. In SmF, the mutant DGRA- 1 showed higher β- fructofuranosidase
productivity (110.8 U/1/hr) than the wild type (48.3 U/I/hr). While in SSF the same
strain produced 322 U/1/hr of β fructofuranosidase,2 times higher than that of
wild type (154.2 U/1/ hr). In SmF, both wildtype and mutants produced
relatively low level of β-fructofuranosidase in medium containing sucrose with
glucose than from the sucrose medium. However in SSF, the DGRA- 1 mutant grown
in sucrose and sucrose + glucose did not show any difference with respect to β-fructofuranosidase
production. These results indicate that the catabolite repression of β- fructofuranosidase
synthesis is observed in SmF whereas in SSF such regulation was not prominent.</span
Phlorotannins from Brown Algae: inhibition of advanced glycation end products formation in high glucose induced <i style="mso-bidi-font-style:normal">Caenorhabditis elegans</i>
371-379Advanced
Glycation End products (AGE) generated in a non enzymatic protein glycation
process are frequently associated with diabetes, aging and other chronic
diseases. Here, we explored the protective effect of phlorotannins from brown
algae Padina pavonica, Sargassum polycystum and Turbinaria ornata against AGEs
formation. Phlorotannins were extracted from brown algae with methanol and its
purity was analyzed by TLC and RP-HPLC-DAD. Twenty five grams of P. pavonica, S. polycystum, T. ornata yielded 27.6±0.8 µg/ml, 37.7 µg/ml and
37.1±0.74 µg/ml of phloroglucinol equivalent of phlorotannins, respectively.
Antioxidant potentials were examined through DPPH assay and their IC50 values
were
P. pavonica (30.12±0.99 µg), S. polycystum (40.9±1.2 µg) and
T. ornata (22.9±1.3 µg), which was
comparatively lesser than the control ascorbic acid (46±0.2 µg).
Further, anti-AGE activity was examined in vitro by BSA-glucose assay with the
extracted phlorotannins of brown algae (P. pavonica, 15.16±0.26 µg/ml;
S. polycystum, 35.245±2.3 µg/ml;
T. ornata,<i style="mso-bidi-font-style:
normal"> 22.7±0.3 µg/ml), which revealed the required concentration to inhibit 50% of albumin
glycation (IC50) were lower for extracts than controls
(phloroglucinol, 222.33±4.9 µg/ml; thiamine, 263 µg/ml). Furthermore, brown algal extracts containing phlorotannins (100 µl)
exhibited protective effects against AGE formation <i style="mso-bidi-font-style:
normal">in vivo in C. elegans
with induced hyperglycemia.<span style="mso-bidi-font-family:
GCFrutiger-Bold" lang="EN-GB">
</span
Production of biodiesel from cyanobacteria (<i>Oscillatoria annae) </i>by alkali and enzyme mediated transesterification
959-967This
study presents lipids from Oscillatoria annae BDU6,
a freshwater cyanobacterium, to generate biodiesel. Efficient oil
extraction
from O. annae was achieved by
ultrasonication in combination with organic solvents (50.9%) than
homogenization
(40.4%).
Efficient conversion of triglycerides of O. annae into
biodiesel was obtained by alkali mediated transesterification (86%
w/v)
when compared with lipase-mediated transesterification (76.5% w/v). RSM and
CCRD were employed to optimize the
growth
medium to improve biomass of O. annae,
which resulted in 3.2-fold increase in biomass yield (5.3 g-l
dry wt/g of inoculum)
compared to initial level (1.6 g-l
dry wt/g of inoculum)
Thermal inactivation of alkali stable xylanases (XylA & XylB) from alkali tolerant fungus Aspergillus fischeri Fxn 1: effect of trehalose on their thermostability
Alkali tolerant fungus Aspergillus fischeri Fxn 1 secretes two xylanases,
an exoxylanase (XylA) and an endoxylanase (XylB) in solid state fermentation.
Kinetic studies showed that thermal inactivation of purified XylA
and XylB at pH 9, in the temperature ranging from 303K to 333K,
followed first-order kinetics, with denaturation rate constants as
9.6 10-3 and 8.2 10-3 at 323K for XylA & XylB respectively. Heat-inactivation
plots for purified enzymes were linear from which
thermodynamic activation parameters, ΔH#, ΔS# and ΔG# have been
estimated. The enzymatic activity was relatively stable with a respective
half-life (t1/2) at 323K of 72 min for XylA and 84.5 min for XylB. The half
life values of XylA & XylB increased to 169 and 136 min respectively, in
the presence of 1 M trehalose. Separate tests at 60
C in the presence of
additives (polyols, carbohydrates) showed that trehalose was the most
effective stabiliser, which increased the stability of XylA & XylB to 64.7 &
17.63 % respectively
Riboflavin Responsive Mitochondrial Dysfunction in Neurodegenerative Diseases
Mitochondria are the repository for various metabolites involved in diverse energy-generating processes, like the TCA cycle, oxidative phosphorylation, and metabolism of amino acids, fatty acids, and nucleotides, which rely significantly on flavoenzymes, such as oxidases, reductases, and dehydrogenases. Flavoenzymes are functionally dependent on biologically active flavin adenine dinucleotide (FAD) or flavin mononucleotide (FMN), which are derived from the dietary component riboflavin, a water soluble vitamin. Riboflavin regulates the structure and function of flavoenzymes through its cofactors FMN and FAD and, thus, protects the cells from oxidative stress and apoptosis. Hence, it is not surprising that any disturbance in riboflavin metabolism and absorption of this vitamin may have consequences on cellular FAD and FMN levels, resulting in mitochondrial dysfunction by reduced energy levels, leading to riboflavin associated disorders, like cataracts, neurodegenerative and cardiovascular diseases, etc. Furthermore, mutations in either nuclear or mitochondrial DNA encoding for flavoenzymes and flavin transporters significantly contribute to the development of various neurological disorders. Moreover, recent studies have evidenced that riboflavin supplementation remarkably improved the clinical symptoms, as well as the biochemical abnormalities, in patients with neuronopathies, like Brown-Vialetto-Van-Laere syndrome (BVVLS) and Fazio-Londe disease. This review presents an updated outlook on the cellular and molecular mechanisms of neurodegenerative disorders in which riboflavin deficiency leads to dysfunction in mitochondrial energy metabolism, and also highlights the significance of riboflavin supplementation in aforementioned disease conditions. Thus, the outcome of this critical assessment may exemplify a new avenue to enhance the understanding of possible mechanisms in the progression of neurodegenerative diseases and may provide new rational approaches of disease surveillance and treatment