20 research outputs found
Effects of in-yolk-sac administration of carvacrol on cholesterol resorption from yolk residuals and physiological adaptive indicators in broiler chicks exposed to neonatal fasting
Three hundred and twenty Ross 308 male broiler chicks were used to examine
effects of in-yolk-sac (IYS) administration of carvacrol on cholesterol
resorption from yolk and physiological adaptive responses of broiler chicks
subjected to post-hatch fasting periods of up to 72 h. Effects of the four
experimental treatments, namely non-handled control (NHCON), sham
injection control (SICON), polysorbate-80 injection (POLS), and carvacrol
injection (CARV), were examined in 5 replicates of 10 birds each. Liver
proportional weight was greater in carvacrol-injected chicks compared with
other birds 24 h post-hatch (<i>P</i> < 0.05). The mean blood glucose
concentration was 199.0 mg dL<sup>−1</sup> when chicks were removed from the hatcher baskets,
and decreased in all birds after being subjected to a 72 h post-hatch fasting.
However, the slope of decrease in serum concentration of glucose was slower
in carvacrol-injected birds than in the other birds, and they had a greater
plasma glucose level compared with NHCON and SICON birds after 72 h
post-hatch fasting. Lower plasma cholesterol levels were observed in
carvacrol-treated chicks compared with those subjected to the other
treatments at 72 h post-hatch (<i>P</i> < 0.05). Blood concentration of
calcium (Ca) was greater in carvacrol-injected birds at 24 h post-hatch than
in NHCON and SICON birds (<i>P</i> <  0.05), but at 72 h it significantly
increased in all birds, with the exception of carvacrol-treated chicks, which
had significantly lower blood Ca concentration (11.17 mg dL<sup>−1</sup>) compared with
other birds (<i>P</i> < 0.05). Blood potassium concentration increased in
polysorbate-80 and carvacrol-injected chicks 24 h post-hatch compared with
the NHCON and SICON birds (<i>P</i> <  0.05). In conclusion, the results of
the current study revealed that there was no direct interaction between
cholesterol and carvacrol leading to reduced cholesterol absorption from
yolk sac in newly hatched broiler chicks
Construction and Characterization of a New Recombinant Vector to Remove Sulfate Repression of dsz Promoter Transcription in Biodesulfurization of Dibenzothiophene
Biodesulfurization (BDS) is an environmentally friendly desulfurizing process with the potential of replacing or adding to the current expensive technologies for sulfur removal from fossil fuels. The BDS, however, still suffers from low biocatalyst activity. One reason is repression of dsz promoter transcription in presence of inorganic sulfate that impedes translation of Dsz enzymes required for desulfurization pathway. One approach to solve this problem is replacing the native promoter with a new promoter that is no longer repressed. In this study, dsz genes from desulfurizing strain Rhodococcus sp. FUM94 was cloned in an alkane responsive promoter, pCom8, and expressed in Escherichia coli BL21 (DE3) as a host. The recombinant was not susceptible to inorganic sulfate in the culture medium. Desulfurizing activity of recombinant strain versus wild type indicated that in a sulfate containing medium, BDS yield of recombinant increased from 16.0% ± 0.9 to 34.0% ± 1.9% when dibenzothiophene (DBT) concentration (dissolved in ethanol) increased from 25 to 100 ppm. Also, 2-hydroxy biphenyl (2-HBP) production rate improved 8.5-fold (from 0.302 ± 0.020 to 2.57 ± 0.14 mmol 2-HBP (kg DCW)-1 h-1) at the same DBT concentration range. This is while no 2-HBP production was detected in FUM94 biphasic reaction. In a sulfate-free medium, wild type strain demonstrated desulfurization activity, but decreasing with the increase of DBT concentration dissolved in n-tetradecane. Whereas, the recombinant strain demonstrated increasing desulfurizing activity in a sulfate-containing high DBT concentration environment. Overall, the result of this molecular manipulation can be considered as a step forward toward commercialization of BDS technology