scholarly journals Integration of heterologous 4-hydroxybenzoic acid transport proteins in Rhodobacter sphaeroides for enhancement of coenzyme Q10production

RSC Advances ◽  
2017 ◽  
Vol 7 (28) ◽  
pp. 17346-17352 ◽  
Author(s):  
Feng Qi ◽  
Limei Zou ◽  
Xianzhang Jiang ◽  
Shaoli Cai ◽  
Mingliang Zhang ◽  
...  
Keyword(s):  
Genetic Engineering ◽  
Membrane Transport ◽  
Rhodobacter Sphaeroides ◽  
Transport Proteins ◽  
Transport Protein ◽  
Hydroxybenzoic Acid ◽  
Acid Transport ◽  
Membrane Transport Protein ◽  
Engineering Strategy

This work provides a novel genetic engineering strategy that improves uptake of extracellular 4-hydroxybenzoic acid by heterologously expressing the membrane transport protein PcaK inR. sphaeroidesfor enhancement of CoQ10production.

scholarly journals Abundant bacterial expression and reconstitution of an intrinsic membrane-transport protein from bovine mitochondria

1993 ◽  
Vol 294 (1) ◽  
pp. 293-299 ◽  
Author(s):  
G Fiermonte ◽  
J E Walker ◽  
F Palmieri
Keyword(s):  
Membrane Transport ◽  
Inclusion Bodies ◽  
Transport Proteins ◽  
Transport Protein ◽  
Site Directed Mutagenesis ◽  
E Coli ◽  
Membrane Transport Protein ◽  
Wide Range ◽  
Competitive Inhibitors ◽  
Oxoglutarate Carrier

The oxoglutarate carrier, an intrinsic membrane-transport protein of the inner membranes of bovine-heart mitochondria, has been expressed at an abundant level in Escherichia coli. It accumulates in the bacterium as inclusion bodies, and none of the protein was detected in the bacterial inner membrane. The mitochondrial ADP/ATP carrier, a member of the same super-family of transport proteins as the oxoglutarate carrier, has also been expressed in E. coli. However, the expression of the ADP/ATP carrier in bacteria retards their growth, and so the levels of expression that were attained were lower than those of the oxoglutarate carrier. The oxoglutarate carrier inclusion bodies have been disaggregated with the detergent N-dodecanoyl-sarcosine, and the protein has been incorporated into liposomes. In its ability to transport oxoglutarate and malate and other known substrates of the carrier in mitochondria, and in its inhibition characteristics by a wide range of non-competitive and competitive inhibitors, this reconstituted oxoglutarate carrier is similar to the natural protein in the inner membranes of mitochondria, and to the carrier that has been purified from mitochondria and reconstituted in liposomes. These experiments remove significant obstacles to crystallization trials and to site-directed mutagenesis of the oxoglutarate carrier.

scholarly journals Manipulating phospholipids for crystallization of a membrane transport protein

2006 ◽  
Vol 103 (6) ◽  
pp. 1723-1726 ◽  
Author(s):  
L. Guan ◽  
I. N. Smirnova ◽  
G. Verner ◽  
S. Nagamori ◽  
H. R. Kaback
Keyword(s):  
Membrane Transport ◽  
Transport Protein ◽  
Membrane Transport Protein
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