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Kadirareddy, Rashmi Holur,GhantaVemuri, Sujana,Palempalli, Uma Maheswari Devi Asian Pacific Journal of Cancer Prevention 2016 Asian Pacific journal of cancer prevention Vol.17 No.7
Conjugated linoleic acid, a functional lipid, produced from Lactobacillus plantarum (LP-CLA), has been demonstrated to possess apoptotic activity. The anti-proliferative and apoptotic potential of LP-CLA was here evaluated in vitro using the MDA-MB-231 human breast cancer cell line as a model system. Proliferation of MDA-MB-231 cells was inhibited with increasing concentrations of LP-CLA with altered morphological features like cell detachment, rounding of cells and oligonucleosomal fragmentation of DNA. Flow cytometry confirmed the apoptotic potential of LP-CLA by ANNEXIN V/PI double staining. Furthermore, outcome results indicated that the apoptosis was mediated by downregulation of the NF-${\kappa}B$ pathway which in turn acted through proteasome degradation of $I{\kappa}B{\alpha}$, inhibition of p65 nuclear translocation, release of cytochrome-C from mitochondria and finally overexpression of Bax protein. Thus, conjugated linoleic acid, a natural product derived from probiotics, could therefore be a possible potential chemotherapeutic agent due to its apoptotic activity against estrogen receptor negative breast cancer cells.
Enhanced Production and Partial Purification of Glucoamylase from Mutated Bacillus sp. FME
Gudi Satheesh Kumar,Muni Ramanna Gari Subhosh Chandra,Yakasiri Nagasai Sujana,Bontha Rajasekhar Reddy,Yong Lark Choi 한국응용생명화학회 2009 Applied Biological Chemistry (Appl Biol Chem) Vol.52 No.5
In this study, a potent newly-isolated glucoamylase producing actively growing cells of Bacillus sp.FME was subjected to UV irradiation and ethidium bromide (EtBr) mutagenesis. The promising colonies were further screened for glucoamylase production via plate assays and submerged enzyme production at the flask level. Amongst all of the tested colonies, the best mutant, Bacillus sp. FME 2, selected from UV irradiation (20 min) and EtBr (1 mg/mL), was shown to be the most promising. The yield of glucoamylase generated by the mutant strain was approximately 3.0 fold and 1397 U/mL with an incubation period of 24 h, which was larger than the yield generated by the wild-type strain. The glucoamylase was partially purified using ammonium sulphate precipitation followed by gel exclusion chromatography. The enzyme was partially purified 3.0-fold to homogeneity with a final recovery of 66% and a specific activity of 1145 U/mg protein for the mutant strain. The molecular mass was approximately 67.1 kDa, as determined by SDS-PAGE. The active band was observed as a clear colorless area on zymogram analysis, which indicated an absence of glucoamylase isoforms. The results of thin-layer chromatography identified this enzyme as a glucoamylase.
Enhanced Production and Partial Purification of Glucoamylase from Mutated Bacillus sp. FME
Kumar, Gudi Satheesh,Chandra, Muni Ramanna Gari Subhosh,Sujana, Yakasiri Nagasai,Reddy, Bontha Rajasekhar,Choi, Yong-Lark The Korean Society for Applied Biological Chemistr 2009 Applied Biological Chemistry (Appl Biol Chem) Vol.52 No.5
In this study, a potent newly-isolated glucoamylase producing actively growing cells of Bacillus sp. FME was subjected to UV irradiation and ethidium bromide (EtBr) mutagenesis. The promising colonies were further screened for glucoamylase production via plate assays and submerged enzyme production at the flask level. Amongst all of the tested colonies, the best mutant, Bacillus sp. FME 2, selected from UV irradiation (20 min) and EtBr (1 mg/mL), was shown to be the most promising. The yield of glucoamylase generated by the mutant strain was approximately 3.0 fold and 1397 U/mL with an incubation period of 24 h, which was larger than the yield generated by the wild-type strain. The glucoamylase was partially purified using ammonium sulphate precipitation followed by gel exclusion chromatography. The enzyme was partially purified 3.0-fold to homogeneity with a final recovery of 66% and a specific activity of 1145 U/mg protein for the mutant strain. The molecular mass was approximately 67.1 kDa, as determined by SDS-PAGE. The active band was observed as a clear colorless area on zymogram analysis, which indicated an absence of glucoamylase isoforms. The results of thin-layer chromatography identified this enzyme as a glucoamylase.
Enhanced Production and Partial Purification of Glucoamylase from Mutated Bacillus sp. FME
( Gudi Satheesh Kumar ),( Muni Ramanna Gari Subhosh Chandra ),( Yakasiri Nagasai Sujana ),( Bontha Rajasekhar Reddy ),( Yong Lark Choi ) 한국응용생명화학회 2009 Applied Biological Chemistry (Appl Biol Chem) Vol.52 No.5
CO2 fixation and lipid production by microalgal species
Srinivasa Reddy Ronda,Pavani Parupudi,Chandrika Kethineni,Pradip Babanrao Dhamole,Sandeep Vemula,Prasada Rao Allu,Mahendran Botlagunta,Sujana Kokilagadda 한국화학공학회 2016 Korean Journal of Chemical Engineering Vol.33 No.2
Microalgal species Nannochloropsis limnetica, Botryococcus braunii, and Stichococcus bacillaris were compared for their ability to grow, remove CO2, and accumulate lipids in their biomass under CO2-enriched atmosphere. Overall, N. limnetica outperformed the other two cultures and distinctly exhibited higher specific growth rate (0.999 d−1) and CO2 fixation rate (0.129 gL−1 d−1) with a high specific lipid yield (40% w/w). The volumetric CO2 fixation rate for all three species was validated with biomass productivity and mass transfer methods (P<0.005 and R2=0. 98). At 10% CO2, N. limnetica showed one-and-a-half times more carbon fixation efficiency over B. braunii, and S. bacillaris. On the other hand, total fatty acids of N. limnetica dispalyed an apparent increase in oleic acid. Whereas, under similar conditions, N. limnetica exhibited reduced eicosapentaenoic acid. These findings suggest that at high CO2 conditions, N. limnetica proved to be an efficient CO2 capture algal system and can be considered for biofuel applications.