Production of α-Amylase from Haloarcula hispanica 2TK2 Strain: Optimization of the Parameters That Effecting Activity

2013 ◽  
Vol 19 (12) ◽  
pp. 3551-3555 ◽  
Author(s):  
Aytun Nilay Erdagi ◽  
Azade Attar ◽  
Yeliz Basaran-Elalmis ◽  
Sevil Yucel ◽  
Meral Birbir
2013 ◽  
Vol 7 (1) ◽  
pp. 29 ◽  
Author(s):  
Mona Yousofshahi ◽  
Michael Orshansky ◽  
Kyongbum Lee ◽  
Soha Hassoun
Keyword(s):  

Author(s):  
Yee Wen Choon ◽  
Mohd Saberi Bin Mohamad ◽  
Safaai Deris ◽  
Rosli Md. Illias ◽  
Lian En Chai ◽  
...  

2013 ◽  
Vol 42 (4) ◽  
pp. 2282-2294 ◽  
Author(s):  
Zhenfang Wu ◽  
Jingfang Liu ◽  
Haibo Yang ◽  
Hailong Liu ◽  
Hua Xiang

Abstract The use of multiple replication origins in archaea is not well understood. In particular, little is known about their specific control mechanisms. Here, we investigated the active replication origins in the three replicons of a halophilic archaeon, Haloarcula hispanica, by extensive gene deletion, DNA mutation and genome-wide marker frequency analyses. We revealed that individual origins are specifically dependent on their co-located cdc6 genes, and a single active origin/cdc6 pairing is essential and sufficient for each replicon. Notably, we demonstrated that the activities of oriC1 and oriC2, the two origins on the main chromosome, are differently controlled. A G-rich inverted repeat located in the internal region between the two inverted origin recognition boxes (ORBs) plays as an enhancer for oriC1, whereas the replication initiation at oriC2 is negatively regulated by an ORB-rich region located downstream of oriC2-cdc6E, likely via Cdc6E-titrating. The oriC2 placed on a plasmid is incompatible with the wild-type (but not the ΔoriC2) host strain, further indicating that strict control of the oriC2 activity is important for the cell. This is the first report revealing diverse control mechanisms of origins in haloarchaea, which has provided novel insights into the use and coordination of multiple replication origins in the domain of Archaea.


2002 ◽  
Vol 68 (12) ◽  
pp. 5843-5859 ◽  
Author(s):  
Christoph Wittmann ◽  
Elmar Heinzle

ABSTRACT A comprehensive approach of metabolite balancing, 13C tracer studies, gas chromatography-mass spectrometry, matrix-assisted laser desorption ionization-time of flight mass spectrometry, and isotopomer modeling was applied for comparative metabolic network analysis of a genealogy of five successive generations of lysine-producing Corynebacterium glutamicum. The five strains examined (C. glutamicum ATCC 13032, 13287, 21253, 21526, and 21543) were previously obtained by random mutagenesis and selection. Throughout the genealogy, the lysine yield in batch cultures increased markedly from 1.2 to 24.9% relative to the glucose uptake flux. Strain optimization was accompanied by significant changes in intracellular flux distributions. The relative pentose phosphate pathway (PPP) flux successively increased, clearly corresponding to the product yield. Moreover, the anaplerotic net flux increased almost twofold as a consequence of concerted regulation of C3 carboxylation and C4 decarboxylation fluxes to cover the increased demand for lysine formation; thus, the overall increase was a consequence of concerted regulation of C3 carboxylation and C4 decarboxylation fluxes. The relative flux through isocitrate dehydrogenase dropped from 82.7% in the wild type to 59.9% in the lysine-producing mutants. In contrast to the NADPH demand, which increased from 109 to 172% due to the increasing lysine yield, the overall NADPH supply remained constant between 185 and 196%, resulting in a decrease in the apparent NADPH excess through strain optimization. Extrapolated to industrial lysine producers, the NADPH supply might become a limiting factor. The relative contributions of PPP and the tricarboxylic acid cycle to NADPH generation changed markedly, indicating that C. glutamicum is able to maintain a constant supply of NADPH under completely different flux conditions. Statistical analysis by a Monte Carlo approach revealed high precision for the estimated fluxes, underlining the fact that the observed differences were clearly strain specific.


2015 ◽  
Vol 113 (3) ◽  
pp. 651-660 ◽  
Author(s):  
Minsuk Kim ◽  
Jeong Sang Yi ◽  
Meiyappan Lakshmanan ◽  
Dong-Yup Lee ◽  
Byung-Gee Kim

2013 ◽  
Vol 110 (11) ◽  
pp. 2938-2948 ◽  
Author(s):  
Shogo Yamamoto ◽  
Masako Suda ◽  
Satoko Niimi ◽  
Masayuki Inui ◽  
Hideaki Yukawa

Archaea ◽  
2017 ◽  
Vol 2017 ◽  
pp. 1-12 ◽  
Author(s):  
Yang Lü ◽  
Hua Lu ◽  
Shiwei Wang ◽  
Jing Han ◽  
Hua Xiang ◽  
...  

A 1.1 × 106 Da acidic exopolysaccharide (EPS) was purified from an extremely halophilic archaeonHaloarcula hispanicaATCC33960 with a production of 30 mg L−1when grown in AS-168 medium, which mainly composed of mannose and galactose with a small amount of glucose in a molar ratio of 55.9 : 43.2 : 0.9. Two glycosyltransferase genes (HAH_1662andHAH_1667) were identified to be responsible for synthesis of the acidic EPS. Deletion of eitherHAH_1662orHAH_1667led to loss of the acidic EPS. The mutants displayed a different cell surface morphology, retarded growth in low salty environment, an increased adhesion, and swimming ability. Our results suggest that biosynthesis of the acidic EPS might act as an adaptable mechanism to protect the cells against harsh environments.


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