Lytic

The blocking and deblocking of carboxyl groups occurs by reactions similar to those described for hydroxyl and amino groups. The most important protected derivatives are /-butyl, benzyl, and methyl esters. These may be cleaved in this order by trifluoroacetic acid, hydrogenolysis, and strong acid or base (J.F.W. McOmie, 1973). 2,2,2-Trihaloethyl esters are cleaved electro-lytically (M.F. Semmelhack, 1972) or by zinc in acetic acid like the Tbeoc- and Tceoc-protected hydroxyl and amino groups. 

Although GGMS is the most widely used ana lytical method that combines a chromatographic sep aration with the identification power of mass spectrometry it is not the only one Chemists have coupled mass spectrometers to most of the mstru ments that are used to separate mixtures Perhaps the ultimate is mass spectrometry/mass spectrome try (MS/MS) m which one mass spectrometer gener ates and separates the molecular ions of the components of a mixture and a second mass spec trometer examines their fragmentation patterns ... 

Insect Cells. In this system the cDNA is inserted into the genome of an insect vims, baculovims. Insect cells, or Hve insect larvae, are then infected with the vims. In this way advantage is taken of the vims s natural machinery for repHcation utilizing the insect cell. This is one of the best systems available for high level production of native protein having post-translational modifications similar to those seen in mammalian cells. Disadvantages of this system include lytic—batch variations, comparatively slow growth, and cosdy scale-up. 

Deep C t lytic Crocking. This process is a variation of fluid catalytic cracking. It uses heavy petroleum fractions, such as heavy vacuum gas oil, to produce propylene- and butylene-rich gaseous products and an aromatic-rich Hquid product. The Hquid product contains predorninantiy ben2ene, toluene, and xylene (see BTX processing). This process is being developed by SINOPEC in China (42,73). SINOPEC is currentiy converting one of its fluid catalytic units into a demonstration unit with a capacity of 60,000 t/yr of vacuum gas oil feedstock. 

Superffex C t lytic Crocking. A new process called Superflex is being commercialized to produce predorninantiy propylene and butylenes from low valued hydrocarbon streams from an olefins complex (74). In this process, raffinates (from the aromatics recovery unit and the B—B stream after the recovery of isobutylene) and pyrolysis gasoline (after the removal of the C —Cg aromatics fraction) are catalyticaHy cracked to produce propylene, isobutylene, and a cmde C —Cg aromatics fraction. AH other by-products are recycled to extinction. 

In acylated form, the APSAC offers a prolonged half-life (105 min), greater lysis potency, and less systemic lytic state. APSAC is used at 30 U (30 mg) by iv injection. 

Recovery. The principal purpose of recovery is to remove nonproteinaceous material from the enzyme preparation. Enzyme yields vary, sometimes exceeding 75%. Most industrial enzymes are secreted by a microorganism, and the first recovery step is often the removal of whole cells and other particulate matter (19) by centrifugation (20) or filtration (21). In the case of ceU-bound enzymes, the harvested cells can be used as is or dismpted by physical (eg, bead mills, high pressure homogenizer) and/or chemical (eg, solvent, detergent, lysozyme [9001 -63-2] or other lytic enzyme) techniques (22). Enzymes can be extracted from dismpted microbial cells, and ground animal (trypsin) or plant (papain) material by dilute salt solutions or aqueous two-phase systems (23). 

The side effects of anistreplase appear to be similar to those of streptokinase, including immune reactions and a systemic lytic state conductive to hemorrhage. 

Tissue Plasminogen Aetivator (tPA). While streptokinase and urokinase can effectively induce clot dissolution in the majority of patients if given early, they lack clot specificity. Treatment with these enzymes results in a systemic lytic state attributable to their degradative action on circulating fibrinogen. Tissue plasminogen activator (tPA) was developed to achieve rapid and specific thrombolysis. 

The present procedure was developed from those of Wallach and Freylon, based upon the general method discovered by Leuckart. a-Phenylethylamine also can be prepared satisfactorily by the reduction of acetophenone oxime with sodium and absolute alcohol or sodium amalgam, but the reagents are more expensive and the processes less convenient. The amine has been obtained by reducing acetophenone oxime electro-lytically, by reducing acetophenone phenylhydrazone with sodium amalgam and acetic acid, from a-phenylethyl bromide and hexamethylenetetramine, and by the action of methyl-magnesium iodide upon hydrobenzamide, as well as by other methods of no preparative value. 

The facility with which a-cleavage occurs in solution depends on the stability of ttae adical fragments that can be ejected. Dibenzyl ketone, for exan le, is readify cleav jjiboto-lytically. Similarly, r-butyl ketones undergo a-cleavage quite readify on p ioCo in solution. ... 

Antibiosis Inhibition or lysis of an organism mediated by metabolic products of the antagonist these products include lytic agents, enzymes, volatile compounds, and other toxic substances. 

It has recently been suggested that a free radical mechanism i.e., homo-lytic cleavage of the oxygen-oxygen bond rather than the heterolytic cleavage pictured) may be involved in the reaction of some substituted benzophenones and peroxyacetic acid. 

Esters and acetylated hydroxyl groups are completely stable under the experimental conditions, but with ketals 10 29,110,112 yields are generally observed in the thermal reaction. Double bonds do not seem to interfere seriously with the course of the reaction provided that the geometric relationship of the free hydroxyl group to the angular methyl group is not changed drastically. In some cases allylic acetoxylation occurs, e.g., at C-7 of A -steroids. ° Ketones are usually stable (especially under photo-lytic conditions) but occasionally a-acetoxylation has been observed. 

The major part of this blister copper is further purified electro lytic ally by casting into anodes which are suspended in acidified CUSO4 solution along with cathodes of purified copper sheet. As electrolysis proceeds the pure copper is deposited on the cathodes while impurities collect below the anodes as anode slime which is a valuable source of Ag, Au and other precious metals. 

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