Growth of microorganisms on insoluble polymers: Transformation of automobile tires

Microorganisms were isolated that transform 35-mesh automobile tire carcasses, utilizing water-soluble oils in the tire particle as a carbon source, while concomitantly oxidizing the styrene-butadiene copolymer of the insoluble substrate by co-metabolism. The product behaved as a cationic exchanger.     

Steady-state methods for the study of placental exchange.

Published and new data on steady-state exchange of tracers and oxygen are characterized by marked species differences. When the placenta is treated as an ideal diffusion cell of unknown vessel geometry and permeability, the exchange characteristics of oxygen can be used to prove that the exchange of tracers such as acetylene, nitrous oxide, tritiated water and antipyrine is entirely flow limited. The recorded patterns of transfer of flow-limited tracers reveal that some placentas are as effective as counter-current exchangers whereas others mimic the behavior of the less effective types of exchangers. These species differences in apparent geometry are unrelated to the histologic nature of the barrier. The patterns of flow-limited transfer are so similar to those of oxygen transfer that the diffusion resistance to oxygen must be small. The exchange of diffusion-limited (hydrophilic) tracers mimics exchange across capillary membranes in some species and exchange across cell membranes in others. These species differences in diffusion-limited transfer are clearly related to the histologic nature of the barrier and are independent of vessel geometry.     

Strategies for the chemoenzymatic preparation of optically active 1-alkyn-3-ols

A series of (R)- and (S)-1-alkyn-3-ols, chiral building units for the synthesis of leukotrienes and pheromones, were prepared via enantioselective hydrolysis of their racemic esters. While the majority of biocatalysts employed (lipases, fermenting or freeze-dried microorganisms) failed in discriminating between enantiomers, lyophilized cells of baker's yeast (Saccharomyces cerevisiae Hansen) gave (S)-1-alkyn-3-ols and their corresponding (R)-esters with greater than 90% e.e.     

Mandelate racemase assayed by polarimetry

An accurate and convenient assay for mandelate racemase based on polarimetry was developed by making use of the time-dependent decrease of the optical rotation of the substrate (D- or L-mandelate) at 589 nm (Na-D-line) during the enzyme-catalyzed racemization. In comparison to the indirect assay methods hitherto used, this method has the following advantages: (i) it is faster and more accurate than the two-enzyme redox assay (which needs a membrane-bound protein fraction), (ii) it is also applicable to non-natural substrates other than mandelate, provided their specific optical rotation is large enough and (iii) it does not rely on expensive equipment such as circular dicroism. © Rapid Science Ltd. 1998     

Development of a polishing step using a hydrophobic interaction membrane adsorber with a PER.C6®‐derived recombinant antibody

Membrane chromatography has already proven to be a powerful alternative to polishing columns in flow‐through mode for contaminant removal. As flow‐through utilization has expanded, membrane chromatography applications have included the capturing of large molecules, including proteins such as IgGs. Such bind‐and‐elute applications imply the demand for high binding capacity and larger membrane surface areas as compared to flow‐through applications. Given these considerations, a new Sartobind Phenyl? membrane adsorber was developed for large‐scale purification of biomolecules based on hydrophobic interaction chromatography (HIC) principles. The new hydrophobic membrane adsorber combines the advantages of membrane chromatography—virtually no diffusion limitation and shorter processing time—with high binding capacity for proteins comparable to that of conventional HIC resins as well as excellent resolution. Results from these studies confirmed the capability of HIC membrane adsorber to purify therapeutic proteins with high dynamic binding capacities in the range of 20 mg‐MAb/cm³‐membrane and excellent impurity reduction. In addition the HIC phenyl membrane adsorber can operate at five‐ to ten‐fold lower residence time when compared to column chromatography. A bind/elute purification step using the HIC membrane adsorber was developed for a recombinant monoclonal antibody produced using the PER.C6® cell line. Loading and elution conditions were optimized using statistical design of experiments. Scale‐up is further discussed, and the performance of the membrane adsorber is compared to a traditional HIC resin used in column chromatography. Biotechnol. Bioeng. 2010; 105: 296–305. © 2009 Wiley Periodicals, Inc.     

Zinc uptake by corn as affected by vesicular-arbuscular mycorrhizae

Pot-grown mycorrhizal and non-mycorrhizal sweet corn were grown in a low Zn soil. All treatments received a complete nutrient solution with or without Zn. Treatments were harvested sequentially to detemine temporal mycorrhizal effects on: (a) tissue and water soluble Zn and (b) differential uptake of P and Zn. Plants grown with supplemental Zn had greater growth and Zn tissue concentration than those not receiving Zn. With no supplemental Zn, mycorrhizal treatments had greater growth and Zn concentration than non-mycorrhizal treatments. There was no indication of nutrient interaction between Zn and P. Over the range of tissue Zn found, there appeared to be no advantage to water soluble Zn analysis over total Zn in assessing plant Zn status.     

Transient repression of the synthesis of OmpF and aspartate transcarbamoylase in Escherichia coli K12 as a response to pollutant stress

Abstract The synthesis of total cellular proteins in Escherichia coli K12 was studied in batch culture following exposure of cells to low concentrations of monochlorophenol, pentachlorophenol and cadmium chloride. Changes in protein patterns were identified after pulse-chase labelling of proteins with [³⁵S]methionine and subsequent two-dimensional gel electrophoresis (2D-PAGE). We demonstrated that besides the induction of some stress proteins, also a transient decrease in the rate of synthesis of other proteins occurred. Two of these proteins were identified as OmpF and aspartate transcarbamoylase (ATCase). Their transient repression appeared to be a general response to stress elicited by different pollutants and may therefore be used as a general and sensitive early warning system for pollutant stress.