Enhanced production of heteropolysaccharide-7 by Beijerinckia indica HS-2001 in pilot-scaled bioreactor under optimized conditions involved in dissolved oxygen using sucrose-based medium

2013 ◽  
Vol 18 (1) ◽  
pp. 94-103 ◽  
Author(s):  
Dae-Young Jung ◽  
Chang-Woo Son ◽  
Sung-Koo Kim ◽  
Wa Gao ◽  
Jin-Woo Lee
2015 ◽  
Vol 43 ◽  
pp. 27-37 ◽  
Author(s):  
Allure Nandini ◽  
D.N. Madhusudhan ◽  
Agsar Dayanand

A thermo tolerant, feather-degrading, newly isolated actinobacterial strain Streptomyces minutiscleroticus DNA38 was investigated for its ability to produce keratinase. Maximum production (283.4 IU) of keratinase by Streptomyces minutiscleroticus DNA38 in starch chicken feathers medium under submerged bioprocess was observed at optimized conditions of pH 9.0 of the medium and 45 °C incubation temperature. Further, an enhanced production (435.8 IU) of keratinase was achieved employing response surface methodology. Combined interactive effect of starch (7.50 g/L), yeast extract (0.74 g/L) and chicken feathers (7.50 g/L) were found to be the critical process variables for enhanced production under central composite design. Chicken feathers showed a direct action and addition of starch and yeast extract to the medium proved effective for a significant increase in the production of keratinase. The purified keratinase was monomeric and had a molecular mass of 29 kDa. The enzyme activity was significantly inhibited after pH 9.0 and temperature 50 °C.


2018 ◽  
Author(s):  
Neil K. Ganju ◽  
Jeremy M. Testa ◽  
Steven E. Suttles ◽  
Alfredo L. Aretxabaleta

Abstract. The light climate in back-barrier estuaries is a strong control on phytoplankton and submerged aquatic vegetation (SAV) growth, and ultimately net ecosystem metabolism. However, quantifying the spatiotemporal variability of light attenuation and net ecosystem metabolism over seasonal timescales is difficult due to sampling limitations and dynamic physical and biogeochemical processes. Differences in the dominant primary producer at a given location (e.g., phytoplankton versus SAV) can also determine diel variations in dissolved oxygen and associated ecosystem metabolism. Over a one year period we measured hydrodynamic properties, biogeochemical variables (fDOM, turbidity, chlorophyll-a fluorescence, dissolved oxygen), and photosynthetically active radiation (PAR) at multiple locations in Chincoteague Bay, Maryland/Virginia, USA, a shallow back-barrier estuary. We quantified light attenuation, net ecosystem metabolism, and timescales of variability for several water properties at paired channel-shoal sites along the longitudinal axis of the bay. The channelized sites, which were dominated by fine bed sediment, exhibited slightly higher light attenuation due to increased wind-wave sediment resuspension. Light attenuation due to fDOM was slightly higher in the northern portion of the bay, while attenuation due to chlorophyll-a was only relevant at one channelized site, proximal to nutrient and freshwater loading. Gross primary production and respiration were highest at the vegetated shoal sites, though enhanced production and respiration were also observed at one channelized, nutrient-enriched site. Production and respiration were nearly balanced throughout the year at all sites, but there was a tendency for net autotrophy at shoal sites, especially during periods of high SAV biomass. Shoal sites, where SAV was present, demonstrated a reduction in gross primary production (GPP) when light attenuation was highest, but GPP at adjacent shoal sites where phytoplankton were dominant was less sensitive to light attenuation. This study demonstrates how extensive continuous physical and biological measurements can help determine metabolic properties in a shallow estuary, including differences in metabolism and oxygen variability between SAV and phytoplankton-dominated habitats.


2013 ◽  
Vol 30 ◽  
pp. 159-164
Author(s):  
Smita Shrestha ◽  
Fedip Shrestha ◽  
Prajwal Rajbhandari ◽  
Ramesh Baral ◽  
Shyam Krishna Suwal ◽  
...  

Yeasts cells isolated from dry yeast were immobilized in alginate and agarose to form beads. The fermentation of ethanol from cheese whey was optimized with respect to temperature, pH, and rpm. A comparative study was performed between immobilized and free cells to get the maximum ethanol production Results revealed that 35°C temperature, 4.5 pH and 60 rpm is the optimized condition for yeast immobilized in agarose bead. Similarly, 35°C temperature, 5.0 pH, 60 rpm is the optimized condition for yeast immobilized in alginate bead and 35°C temperature, 5.0 pH, 80 rpm is the optimized condition for the free yeast cell respectively. Immobilised cell resulted 4.25% ethanol with alginate bead whereas 4.35% with agarose bead and 4.30% with free cell after three days of incubation under optimized conditions. When the same cell immobilized beads were reused, obtained 1.8% ethanol with agarose and 1.7% ethanol with alginate bead.DOI: http://dx.doi.org/10.3126/jncs.v30i0.9388Journal of Nepal Chemical Society Vol. 30, 2012 Page:  159-164 Uploaded date: 12/20/2013   


2016 ◽  
Vol 92 (6) ◽  
pp. 1464-1471 ◽  
Author(s):  
Jun Xia ◽  
Xiaoyan Liu ◽  
Jiaxing Xu ◽  
Jiming Xu ◽  
Xingfeng Wang ◽  
...  

2021 ◽  
Author(s):  
Sukhyeong Cho ◽  
Yun Seo Lee ◽  
Hanyu Chai ◽  
Sang eun Lim ◽  
Jeong Geol Na ◽  
...  

Abstract Background: Ectoine (1,3,4,5-tetrahydro-2-methyl-4-pyrimidinecarboxylic acid) is an attractive compatible solute because of its wide industrial applications. Previous studies on the microbial production of ectoine have focused on sugar fermentation. Alternatively, methane can be used as an inexpensive and abundant resource for ectoine production by using the halophilic methanotroph, Methylomicrobium alcaliphilum 20Z. However, there are some limitations, including the low production of ectoine from methane and the limited tools for the genetic manipulation of methanotrophs to facilitate their use as industrial strains.Results: We constructed a genetically tractable M. alcaliphilum 20Z with a high conjugation efficiency and stability of the episomal plasmid by the removal of its native plasmid. To improve the ectoine production in M. alcaliphilum 20Z from methane, the ectD (encoding ectoine hydroxylase) and ectR (transcription repressor of the ectABC-ask operon) were deleted to reduce the formation of by-products (such as hydroxyectoine) and induce ectoine production. When the double mutant was batch cultured with methane, ectoine production was enhanced 1.6-fold compared to that obtained with M. alcaliphilum 20ZDP (45.58 mg/L vs. 27.26 mg/L) without growth inhibition. Notably, the use of an optimized medium for ectoine production, containing 6% NaCl and 0.05 µM tungsten, gave ectoine yields of up to 142.32 mg/L without hydroxyectoine production. This result demonstrates the highest ectoine production from methane to date.Conclusions: Ectoine production was significantly enhanced by the disruption of the ectD and ectR genes in M. alcaliphilum 20Z under optimized conditions favoring ectoine accumulation. We demonstrated effective genetic engineering in a methanotrophic bacterium, with enhanced production of ectoine from methane as the sole carbon source. This study suggests a potentially transformational path to commercial sugar-based ectoine production.


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