scholarly journals Elucidating the Phosphate Binding Mode of Phosphate-Binding Protein: The Critical Effect of Buffer Solution

2018 ◽  
Vol 122 (24) ◽  
pp. 6371-6376 ◽  
Author(s):  
Rui Qi ◽  
Zhifeng Jing ◽  
Chengwen Liu ◽  
Jean-Philip Piquemal ◽  
Kevin N. Dalby ◽  
...  
Keyword(s):  
Binding Protein ◽  
Binding Mode ◽  
Phosphate Binding ◽  
Buffer Solution ◽  
Critical Effect ◽  
Phosphate Binding Protein

scholarly journals The high-affinity phosphate-binding protein PstS is accumulated under high fructose concentrations and mutation of the corresponding gene affects differentiation in Streptomyces lividans

Microbiology ◽  
2005 ◽  
Vol 151 (8) ◽  
pp. 2583-2592 ◽  
Author(s):  
Margarita Díaz ◽  
Ana Esteban ◽  
José Manuel Fernández-Abalos ◽  
Ramón I. Santamaría
Keyword(s):  
Culture Media ◽  
Binding Protein ◽  
Protein Pattern ◽  
Phosphate Transport ◽  
Streptomyces Lividans ◽  
Null Mutant ◽  
Phosphate Binding ◽  
Genetic Switch ◽  
High Affinity ◽  
Phosphate Binding Protein

The secreted protein pattern of Streptomyces lividans depends on the carbon source present in the culture media. One protein that shows the most dramatic change is the high-affinity phosphate-binding protein PstS, which is strongly accumulated in the supernatant of liquid cultures containing high concentrations (>3 %) of certain sugars, such as fructose, galactose and mannose. The promoter region of this gene and that of its Streptomyces coelicolor homologue were used to drive the expression of a xylanase in S. lividans that was accumulated in the culture supernatant when grown in the presence of fructose. PstS accumulation was dramatically increased in a S. lividans polyphosphate kinase null mutant (Δppk) and was impaired in a deletion mutant lacking phoP, the transcriptional regulator gene of the two-component phoR-phoP system that controls the Pho regulon. Deletion of the pstS genes in S. lividans and S. coelicolor impaired phosphate transport and accelerated differentiation and sporulation on solid media. Complementation with a single copy in a S. lividans pstS null mutant returned phosphate transport and sporulation to levels similar to those of the wild-type strain. The present work demonstrates that carbon and phosphate metabolism are linked in the regulation of genes and that this can trigger the genetic switch towards morphogenesis.

A Dynamical Investigation of Acrylodan-Labeled Mutant Phosphate Binding Protein

1999 ◽  
Vol 71 (3) ◽  
pp. 589-595 ◽  
Author(s):  
Jeffrey S. Lundgren ◽  
Lyndon L. E. Salins ◽  
Irina Kaneva ◽  
Sylvia Daunert
Keyword(s):  
Binding Protein ◽  
Phosphate Binding ◽  
Phosphate Binding Protein

scholarly journals Preliminary time-of-flight neutron diffraction studies ofEscherichia coliABC transport receptor phosphate-binding protein at the Protein Crystallography Station

2014 ◽  
Vol 70 (6) ◽  
pp. 819-822 ◽  
Author(s):  
K. H. Sippel ◽  
J. Bacik ◽  
F. A. Quiocho ◽  
S. Z. Fisher
Keyword(s):  
Neutron Diffraction ◽  
Binding Protein ◽  
Protein Crystallography ◽  
Phosphate Transport ◽  
Phosphate Binding ◽  
Science Center ◽  
Data Set ◽  
Acceptor Group ◽  
Phosphate Binding Protein ◽  
Ph Range

Inorganic phosphate is an essential molecule for all known life. Organisms have developed many mechanisms to ensure an adequate supply, even in low-phosphate conditions. In prokaryotes phosphate transport is instigated by the phosphate-binding protein (PBP), the initial receptor for the ATP-binding cassette (ABC) phosphate transporter. In the crystal structure of the PBP–phosphate complex, the phosphate is completely desolvated and sequestered in a deep cleft and is bound by 13 hydrogen bonds: 12 to protein NH and OH donor groups and one to a carboxylate acceptor group. The carboxylate plays a key recognition role by accepting a phosphate hydrogen. PBP phosphate affinity is relatively consistent across a broad pH range, indicating the capacity to bind monobasic (H2PO4−) and dibasic (HPO42−) phosphate; however, the mechanism by which it might accommodate the second hydrogen of monobasic phosphate is unclear. To answer this question, neutron diffraction studies were initiated. Large single crystals with a volume of 8 mm3were grown and subjected to hydrogen/deuterium exchange. A 2.5 Å resolution data set was collected on the Protein Crystallography Station at the Los Alamos Neutron Science Center. Initial refinement of the neutron data shows significant nuclear density, and refinement is ongoing. This is the first report of a neutron study from this superfamily.

Evaluation of phosphate removal from water by immobilized phosphate-binding protein PstS

2000 ◽  
Vol 90 (6) ◽  
pp. 688-690 ◽  
Author(s):  
Akio Kuroda ◽  
Hirokazu Kunimoto ◽  
Tomohiro Morohoshi ◽  
Tsukasa Ikeda ◽  
Junichi Kato ◽  
...  
Keyword(s):  
Binding Protein ◽  
Phosphate Removal ◽  
Phosphate Binding ◽  
Phosphate Binding Protein
Sign in / Sign up

Export Citation Format

Share Document