6 research outputs found
Transition of amyloid/mutant p53 from tumor suppressor to an oncogene and therapeutic approaches to ameliorate metastasis and cancer stemness
Abstract The tumor suppressor p53 when undergoes amyloid formation confers several gain-of-function (GOF) activities that affect molecular pathways crucial for tumorigenesis and progression like some of the p53 mutants. Even after successful cancer treatment, metastasis and recurrence can result in poor survival rates. The major cause of recurrence is mainly the remnant cancer cells with stem cell-like properties, which are resistant to any chemotherapy treatment. Several studies have demonstrated the role of p53 mutants in exacerbating cancer stemness properties and epithelial-mesenchymal transition in these remnant cancer cells. Analyzing the amyloid/mutant p53-mediated signaling pathways that trigger metastasis, relapse or chemoresistance may be helpful for the development of novel or improved individualized treatment plans. In this review, we discuss the changes in the metabolic pathways such as mevalonate pathway and different signaling pathways such as TGF-β, PI3K/AKT/mTOR, NF-κB and Wnt due to p53 amyloid formation, or mutation. In addition to this, we have discussed the role of the regulatory microRNAs and lncRNAs linked with the mutant or amyloid p53 in human malignancies. Such changes promote tumor spread, potential recurrence, and stemness. Importantly, this review discusses the cancer therapies that target either mutant or amyloid p53, restore wild-type functions, and exploit the synthetic lethal interactions with mutant p53
Studies on Substrate Specificity and Activity Regulating Factors of Trehalose-6-Phosphate Synthase of Saccharomyces Cerevisiae
Purified trehalose-6-phosphate synthase (TPS) of Saccharomyces cerevisiae was effective over a wide range of
substrates, although differing with regard to their relative activity. Polyanions heparin and chondroitin
sulfate were seen to stimulate TPS activity, particularly when a pyrimidine glucose nucleotide like UDPG was
used, rather than a purine glucose nucleotide like GDPG. A high Vmax and a low Km value of UDPG show its
greater affinity with TPS than GDPG or TDPG. Among the glucosyl acceptors TPS showed maximum activity
with G-6-P which was followed by M-6-P and F-6-P. Effect of heparin was also extended to the purification of
TPS activity, as it helped to retain both stability and activity of the final purified enzyme. Metal co-factors,
specifically MnCl2 and ZnCl2 acted as stimulators, while enzyme inhibitors had very little effect on TPS
activity. Metal chelators like CDTA, EGTA stimulated enzyme activity by chelation of metal inhibitors.
Temperature and pH optima of the purified enzyme were determined to be 40 °C and pH 8.5 respectively.
Enzyme activity was stable at 0–40 °C and at alkaline pH
Purification and Characterization of a Trehalase–Invertase Enzyme with Dual Activity from Candida Utilis
Trehalose and sucrose, two important anti-stress non-reducing natural disaccharides, are catabolized by
two enzymes, namely trehalase and invertase respectively. In this study, a 175 kDa enzyme protein active
against both substrates was purified from wild type Candida utilis and characterized in detail. Substrate
specificity assay and activity staining revealed the enzyme to be specific for both sucrose and trehalose.
The ratio between trehalase and invertase activity was found to be constant at 1:3.5 throughout the
entire study. Almost 40-fold purification and 30% yield for both activities were achieved at the final step
of purification. The presence of common enzyme inhibitors, thermal and pH stress had analogous effects
on its trehalase and invertase activity. Km values for two activities were similar while Vmax and Kcat also
differed by a factor of 3.5. Competition plot for both substrates revealed the two activities to be occurring
at the single active site. N-terminal sequencing and MALDI-TOF data analysis revealed higher similarity of
the purified protein to previously known neutral trehalases. While earlier workers mentioned independent
purification of neutral trehalase or invertase from different sources, the present study reports the
purification of a single protein showing dual activity
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Adaptive laboratory evolution of the fast-growing cyanobacterium Synechococcus elongatus PCC 11801 for improved solvent tolerance.
Cyanobacteria hold promise as cell factories for the photoautotrophic conversion of carbon dioxide to useful chemicals. For the eventual commercial viability of such processes, cyanobacteria need to be engineered for (i) efficient channeling of carbon flux toward the product of interest and (ii) improved product tolerance, the latter being the focus of this study. We chose the recently reported, fast-growing, high light and CO2 tolerant cyanobacterium Synechococcus elongatus PCC 11801 for adaptive laboratory evolution. In two parallel experiments that lasted over 8400 h of culturing and 100 serial passages, S. elongatus PCC 11801 was evolved to tolerate 5 g/L n-butanol or 30 g/L 2,3-butanediol representing a 100% improvement in concentrations tolerated. The evolved strains retained alcohol tolerance even after being passaged several times without the alcohol stress suggesting that the changes were permanent. Whole genome sequencing of the n-butanol evolved strains revealed mutations in a number of stress responsive genes encoding translation initiation factors, RpoB and an ABC transporter. In 2,3-butanediol evolved strains, genes for ClpC, a different ABC transporter, glyceraldehyde-3-phosphate dehydrogenase and phosphoribulokinase were found to be mutated. Furthermore, the evolved strains showed significant improvement in tolerance toward several other alcohols. Notably, the n-butanol evolved strain could tolerate up to 32 g/L ethanol, thereby making it a promising host for photosynthetic production of biofuels via metabolic engineering