The Chemistry of Sites Binding Rubidium in Chlorella

نویسنده

  • Dan Cohen
چکیده

The chemistry of sites that specifically bind Rb in Chlorella pyrenoidosa has been investigated by changing or modifying specific chemical groups or bonds in the cell and observing changes in binding capacity. Boiling the cells in water or in 70 per cent ethanol did not affect binding capacities of the sites. These results suggest that the integrity of the sites is independent of both hydrogen bonds and hydrophobic bonds, and that the sites, therefore, do not consist of a protein or protein-lipid complex. At 30 degrees C, both 1 M HCL and 0.5 to 1 M NaOH rapidly inactivated 70 per cent of the sites, but over a range of Ph 4.4 to 11.3, there was no effect. The sites are inactivated by strong chelating agents at 0.05 to 0.2 M and by reagents which reduce trivalent iron, and 4 to 10 atoms of iron per site are removed from the cells. Prolonged incubation in iron solutions, but not in solutions of Cu, Mn, or Mg, reversed to a considerable extent inactivation by EDTA. It is suggested that the sites probably bind trivalent iron tightly as chelation bridges which are essential to their structure. These structural bridges are broken when iron is removed by chelating agents or reduction, and are reformed in the presence of iron. Other experimental evidence indicates that amine, sulfhydryl, and carbonyl groups are not structural components of the sites.

برای دانلود رایگان متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Specific Binding of Rubidium in Chlorella

Specific binding sites for potassium, which may be components of the carriers for active transport for K in Chlorella, were characterized by their capacity to bind rubidium. A dense suspension was allowed to take up Rb(86) from a low concentration of Rb(86) and a high concentration of ions which saturate non-specific sites. The amount bound was derived from the increase in the external concentr...

متن کامل

Molecular dynamics simulation and docking studies on the binding properties of several anticancer drugs to human serum albumin

Disposition and transportation of anticancer drugs by human serum albumin (HSA) affects their bioavailability, distribution and elimination. In this study, the interaction of a set of anticancer drugs with HSA was investigated by molecular dynamics and molecular docking simulations. The drugs' activities were analyzed according to their docking scores, binding sites and structural descriptors. ...

متن کامل

Putative Binding Sites of Dopamine and Arachidonoyl Dopamine to Beta-lactoglobulin: A Molecular Docking and Molecular Dynamics Study

Because of participation in many aspects of human life, and due to oxidation-sensitive characteristics of dopamine (DA) and arachidonoyl dopamine (AA-DA), the necessity of biocompatible carrier to keep them against oxidation is of importance. In this work, we explored the putative binding sites of DA and AA-DA to -lactoglobulin (BLG) as potent carrier. Docking results identified the binding si...

متن کامل

Studies of In-Vitro Amlodipine and Arsenic Displacement Interaction at Binding Sites of Bovine Serum Albumin

In this study, the binding of amlodipine (a Ca ++ channel Blocker) and arsenic (metalloid) to bovine serum albumin (BSA) was studied by equilibrium dialysis(ED) method in order to have an insight into their binding chemistry to BSA. Free amlodipine concentration was increased due to addition of arsenic which reduced the binding of the compounds to BSA. However, the free fraction was not increa...

متن کامل

Metal ions binding study on human growth hormone by isothermal titration calorimetric method

The interaction of hGH with some metal ions ( ) at 27°C in NaC1 solution, 50 mM was studied using Isothermal titration calorimetry. There is a set of three identical and non-interacting binding sites for binding of all these metal ions, expect . The intrinsic association equilibrium constants () are not very different for  and , and also their molar enthalpies of binding (KJ/mol for  and  KJ/mo...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

عنوان ژورنال:
  • The Journal of General Physiology

دوره 45  شماره 

صفحات  -

تاریخ انتشار 1962