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•Biodiesel is a renewable and ecofriendly biofuel.•It can be produced using transesterification, emulsification and pyrolysis process etc.•Enzyme catalyzed and biomass derived ...catalysts reactions are economic and ecofriendly.•Process intensification technology results in higher yield with lower wastes.
Biodiesel is a non-toxic renewable energy source that is gaining attention globally owing to its direct applicability in preexisting engines without any modification. Various technologies from laboratory scale to industrial scale have been developed, and many plants have been established for biodiesel production using various feedstocks. Using biobased technology in biodiesel production is advantageous as these methods generate less waste and are considered ecofriendly. This article mainly discusses the availability of various oil resources (edible, non-edible, waste cooking oils (WCO)) and the advancements in technology related to oil extraction. Specifically, biobased methods, such as immobilized enzymes (matrix) and heterogeneous catalysts (derived from biomass), reported to catalyze the transesterification reaction for biodiesel production are discussed in detail. Biodiesel production using conventional technologies results in low yield and purity and is time-consuming. Newly introduced process intensification technologies (microreactor, membrane reactor, microwave, reactive distillation, and centrifugal contractor) to overcome these issues are also discussed. The need to develop integrated process technologies for biodiesel production to make the process more economical is emphasized.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
2.
Stem Cell Quiescence LING LI; BHATIA, Ravi
Clinical cancer research,
08/2011, Volume:
17, Issue:
15
Journal Article
Peer reviewed
Open access
Adult stem cells are maintained in a quiescent state but are able to exit quiescence and rapidly expand and differentiate in response to stress. The quiescent state appears to be necessary for ...preserving the self-renewal of stem cells and is a critical factor in the resistance of cancer stem cells (CSCs) to chemotherapy and targeted therapies. Limited knowledge about quiescence mechanisms has prevented significant advances in targeting of drug-resistant quiescent CSCs populations in the clinic. Thus, an improved understanding of the molecular mechanisms of quiescence in adult stem cells is critical for the development of molecularly targeted therapies against quiescent CSCs in different cancers. Recent studies have provided a better understanding of the intrinsic and extrinsic regulatory mechanisms that control stem cell quiescence. It is now appreciated that the p53 gene plays a critical role in regulating stem cell quiescence. Other intrinsic regulatory mechanisms include the FoxO, HIF-1α, and NFATc1 transcription factors and signaling through ATM and mTOR. Extrinsic microenvironmental regulatory mechanisms include angiopoietin-1, TGF-β, bone morphogenic protein, thrombopoietin, N-cadherin, and integrin adhesion receptors; Wnt/β-catenin signaling; and osteopontin. In this article, we review current advances in understanding normal stem cell quiescence, their significance for CSC quiescence and drug resistance, and the potential clinical applications of these findings.
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•Renewable energy seems a promising approach to fulfill the future energy demand.•Biochar is an economic, and efficient material for energy production.•It can be utilized for ...electrode preparation used in MFC.•Biochar is also used as a catalyst for biodiesel and hydrogen production.•Need to work on technology for biochar synthesis with desired properties.
Tremendous population growth and industrialization have increased energy consumption unprecedentedly. The depletion of fossil-based energy supplies necessitates the exploration of solar, geothermal, wind, hydrogen, biodiesel, etc. as a clean and renewable energy source. Most of these energy sources are intermittent, while bioelectricity, biodiesel, and biohydrogen can be produced using abundantly available organic wastes regularly. The production of various energy resources requires materials that are costly and affect the applicability at a large scale. Biomass-derived materials (biochar) are getting attention in the field of bioenergy due to their simple method of synthesis, high surface area, porosity, and availability of functional groups for easy modification. Biochar synthesis using various techniques is discussed and their use as an electrode (anodic/cathodic) in a microbial fuel cell (MFC), catalysts in transesterification, and anaerobic digestion for energy production are reviewed. Renewable energy production using biochar would be a sustainable approach to create an energy secure world.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
5.
My memorable patient Bhatia, Ravi
Indian Pediatrics Case Reports,
2021, Volume:
1, Issue:
4
Journal Article
Chronic myeloid leukemia (CML) originates in a hematopoietic stem cell (HSC) transformed by the breakpoint cluster region (BCR)-abelson (ABL) oncogene and is effectively treated with tyrosine kinase ...inhibitors (TKIs). TKIs do not eliminate disease-propagating leukemic stem cells (LSCs), suggesting a deeper understanding of niche-dependent regulation of CML LSCs is required to eradicate disease. Cxcl12 is expressed in bone marrow niches and controls HSC maintenance, and here, we show that targeted deletion of Cxcl12 from mesenchymal stromal cells (MSCs) reduces normal HSC numbers but promotes LSC expansion by increasing self-renewing cell divisions, possibly through enhanced Ezh2 activity. In contrast, endothelial cell-specific Cxcl12 deletion decreases LSC proliferation, suggesting niche-specific effects. During CML development, abnormal clusters of colocalized MSCs and LSCs form but disappear upon Cxcl12 deletion. Moreover, MSC-specific deletion of Cxcl12 increases LSC elimination by TKI treatment. These findings highlight a critical role of niche-specific effects of Cxcl12 expression in maintaining quiescence of TKI-resistant LSC populations.
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•CXCL12 deletion from mesenchymal stromal cells (MSCs) expands leukemia stem cells•LSCs undergo increased self-renewing divisions, related to enhanced EZH2 activity•CXCL12 deletion from MSCs increases LSC elimination by TKI treatment•CXCL12+ MSC niches are critical for maintaining quiescent, TKI-resistant LSCs
Leukemia stem cells (LSCs) resist elimination by tyrosine kinase inhibitor (TKI) treatment. Bhatia and colleagues report that CXCL12 deletion from mesenchymal stromal cells (MSCs) reduces LSC colocalization, enhances LSC cycling, and increases LSC elimination by TKI treatment, indicating that CXCL12-expressing MSC niches are critical for maintaining quiescent, TKI-resistant LSCs.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
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•Algae can capture carbon dioxide and produce many valuable compounds.•Residual algal biomass is rich in various polysaccharides.•Biomass requires various pretreatments to release ...free sugars.•Algal hydrolysate can be used as feedstock for microbial fermentation.•Hydrolysate can be valorised into bioenergy and biochemicals.
Urbanization and pollution are the major issues of the current time own to the exhaustive consumption of fossil fuels which have a detrimental effect on the nation's economies and air quality due to greenhouse gas (GHG) emissions and shortage of energy reserves. Algae, an autotrophic organism provides a green substitute for energy as well as commercial products. Algal extracts become an efficient source for bioactive compounds having anti-microbial, anti-oxidative, anti-inflammatory, and anti-cancerous potential. Besides the conventional approach, residual biomass from any algal-based process might act as a renewable substrate for fermentation. Likewise, lignocellulosic biomass, algal biomass can also be processed for sugar recovery by different pre-treatment strategies like acid and alkali hydrolysis, microwave, ionic liquid, and ammonia fiber explosion, etc. Residual algal biomass hydrolysate can be used as a feedstock to produce bioenergy (biohydrogen, biogas, methane) and biochemicals (organic acids, polyhydroxyalkanoates) via microbial fermentation.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
With the growing use of fossil fuels and industrial activity, the amount of carbon dioxide (CO2) emission is continuously increasing and is considered a primary contributor to climate change. CO2 ...emissions from stationary resources (coal fire, cement plants, and other industry) can be reduced by using various carbon capture and sequestration (CCS) technologies. In this article, recent advancements in various biological methods (i.e., carbonic anhydrase (CA), hydrogenation of CO2 to formate, reduction of CO2 to methane, CO2 conversion into methanol by enzyme cascade, and the role of RuBisCo enzyme) that have been reported for CO2 capture are discussed, along with their advantages and limitations. A brief overview of other physicochemical (absorption, adsorption, cryogenic, and membrane) technologies is also provided. Although biological methods are ecofriendly and can be performed under ambient conditions, these approaches are still not cost effective, as the reactions require cofactors, and the enzymes lose activity when exposed to hot flue gas and ionic liquids. Most captured CO2 is stored by mineralization using a geological and ocean storage method without providing any economic benefit. It is a question of interest as to how we can utilize CO2 and generate revenue. Utilization of CO2 as a feedstock to produce bioenergy is a possible approach. Various microbes capable of utilizing CO2 as feedstock and producing biofuels (biodiesel and bioalcohol) have been reported. These two technologies, i.e., CO2 capture and bioconversion of CO2 into bioenergy, can be integrated to develop a process that not only mitigates CO2 effects on the environment but also solves energy problems while generating revenue.
•Carbon dioxide (CO2) is contributing in global warming.•CO2 can be used as a resource for bioenergy production.•Electro-biological and integrated system are efficient methods for CO2 to bioenergy conversion.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
The bone marrow microenvironment is composed of heterogeneous cell populations of non-hematopoietic cells with complex phenotypes and undefined trajectories of maturation. Among them, mesenchymal ...cells maintain the production of stromal, bone, fat, and cartilage cells. Resolving these unique cellular subsets within the bone marrow remains challenging. Here, we used single-cell RNA sequencing of non-hematopoietic bone marrow cells to define specific subpopulations. Furthermore, by combining computational prediction of the cell state hierarchy with the known expression of key transcription factors, we mapped differentiation paths to the osteocyte, chondrocyte, and adipocyte lineages. Finally, we validated our findings using lineage-specific reporter strains and targeted knockdowns. Our analysis reveals differentiation hierarchies for maturing stromal cells, determines key transcription factors along these trajectories, and provides an understanding of the complexity of the bone marrow microenvironment.
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GEOZS, IJS, IMTLJ, KILJ, KISLJ, NLZOH, NUK, OILJ, PNG, SAZU, SBCE, SBJE, UILJ, UL, UM, UPCLJ, UPUK, ZAGLJ, ZRSKP
Purpose Philadelphia chromosome (Ph) -like acute lymphoblastic leukemia (ALL) is a high-risk subtype of childhood ALL characterized by kinase-activating alterations that are amenable to treatment ...with tyrosine kinase inhibitors. We sought to define the prevalence and genomic landscape of Ph-like ALL in adults and assess response to conventional chemotherapy. Patients and Methods The frequency of Ph-like ALL was assessed by gene expression profiling of 798 patients with B-cell ALL age 21 to 86 years. Event-free survival and overall survival were determined for Ph-like ALL versus non-Ph-like ALL patients. Detailed genomic analysis was performed on 180 of 194 patients with Ph-like ALL. Results Patients with Ph-like ALL accounted for more than 20% of adults with ALL, including 27.9% of young adults (age 21 to 39 years), 20.4% of adults (age 40 to 59 years), and 24.0% of older adults (age 60 to 86 years). Overall, patients with Ph-like ALL had an inferior 5-year event-free survival compared with patients with non-Ph-like ALL (22.5% 95% CI, 14.9% to 29.3%; n = 155 v 49.3% 95% CI, 42.8% to 56.2%; n = 247, respectively; P < .001). We identified kinase-activating alterations in 88% of patients with Ph-like ALL, including CRLF2 rearrangements (51%), ABL class fusions (9.8%), JAK2 or EPOR rearrangements (12.4%), other JAK-STAT sequence mutations (7.2%), other kinase alterations (4.1%), and Ras pathway mutations (3.6%). Eleven new kinase rearrangements were identified, including four involving new kinase or cytokine receptor genes and seven involving new partners for previously identified genes. Conclusion Ph-like ALL is a highly prevalent subtype of ALL in adults and is associated with poor outcome. The diverse range of kinase-activating alterations in Ph-like ALL has important therapeutic implications. Trials comparing the addition of tyrosine kinase inhibitors to conventional therapy are required to evaluate the clinical utility of these agents in the treatment of Ph-like ALL.
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