Sterilization of Bacillus spores by converted X rays

Relative sensitivities of endospores of Bacillus pumilus E601, B. subtilis IAM1069, B. megaterium S31 and B. brevis S5 to gamma rays, converted X rays (bremsstrahlung) and electron beams were examined in order to estimate the conditions in which converted X rays kill Bacillus spores. The radiation sensitivities to gamma rays and electron beams of each strain dried on glass fiber filter without additives were found to be almost equivalent, and D values were obtained as follows: 1.5–1.6 kGy for B. pumilus, 1.4–1.5 kGy for B. subtilis, 1.9–2.0 kGy for B. megaterium and 1.6–2.0 kGy for B. brevis. The radiation sensitivities of endospores of each strain to electron beams were slightly lower than those to gamma rays in the dry condition with additives of 2% peptone + 1 % glycerin on glass fiber filters. The increase of radiation resistance in the presence of additives was also observed with X rays, and it was on an intermediate level between those with gamma rays and electron beams. In the dry condition using cellulose filter paper, only the radiation resistances of B. megaterium and B. brevis in the presence of additives B. megaterium and B. brevis in the presence of additives were increased.     

EFFECT OF PHOSPHATE ION ON FLUORESCENT CHARACTERISTICS OF TYROSINE AND ITS CONJUGATE BASE

Abstract—The UV fluorescence spectrum of tyrosine (Tyr) is markedly affected by the interaction with phosphate ion. In order to elucidate the mechanism of the specific fluorescence quenching by phosphate and the simultaneous appearance of a new emission, the effect of phosphate on the spectro-scopic characteristics of Tyr was investigated. Employing a fluorimetric method, we have obtained the following results. Namely, potassium phosphate was found to enhance the fluorescence intensity of tyrosinate ion. When Tyr is excited in the phosphate-containing solution, the emission with a peak around 345 nm is observed besides the normal fluorescence of Tyr around 303 nm with a reduced quantum yield. The abnormal emission may be ascribed to the tyrosinate ion in the excited state resulting from the deprotonation of the phenolic OH group of the excited Tyr. although the tyrosinate ion in the ground state is not predominant in the aqueous solution examined.     

Facile formation of chiral calixarene analogs incorporating cystine peptide into the macrocyclic ring

Chiral calixarene analogs incorporating cystine peptide into their macrocyclic ring were easily prepared by the cyclization reactions of bis(chloromethyl)phenol-formaldehyde oligomers with cystine peptides in moderate yields. Circular dichroism (CD) spectra indicated the existence of the transmission of the chirality from peptide unit to phenol-formaldehyde oligomer moiety.     

Synthesis of new ethynylene-containing aromatic polyamides by palladium-catalyzed polycondensation of aromatic diiodides with aromatic diethynyl compounds having amide units

New ethynylene-containing aromatic polymides were synthesized by the carbon–carbon crosscoupling polycondensation of aromatic diiodides with aromatic amide-bearing diethynyl compounds in the presence of a palladium catalyst, cuprous iodide, and an organic base. The polymers having sulfone linkages were soluble in various organic solvents and their weight average molecular weights were in the range of 12,500 and 26,500. The polymers with the highest inherent viscosity were obtained, when the monomer ratio of a diethynyl compound to a diiodide was 1.01. The polymers showed no detectable glass transition temperature and no weight loss up to around 300° C in nitrogen. The thermal crosslinking of the polymers occurred at 280°C through the existing internal ethynylene group. © 1995 John Wiley & Sons, Inc.     

Syntheses of cystothiazole A and its stereoisomers: importance of stereochemistry for antifungal activity

The enantiocontrolled total syntheses of all the stereoisomers of a myxobacterial antibiotic, cystothiazole A, are described. The natural syn stereochemistry at the C4-C5 position was controlled by the asymmetric Evans aldol process, whereas the anti relationship was introduced by a modified Evans aldol methodology. Starting with a known aldehyde, the common substrate of the aldol reactions, cystothiazole A and its three stereoisomers were synthesized in 9 steps. All three stereoisomers did not show antifungal activity even at a dosage 2500-fold that of cystothiazole A.     

Kinetic equation in the kinetic region of the dilute and nonuniform electron plasma

Mori's scaling method is used to derive the kinetic equation for a dilute, nonuniform electron plasma in the kinetic region where the space-time cutoff (b, t _c) satisfies _Dbl _f , _D t _{c f} , with _D the Debye length, _D ^–1= _p the plasma frequency, andl _f and _f the mean free path and time, respectively. The kinetic equation takes account of the nonuniformity of the order ofl _f and _D for the single-and the two-particle distribution function, respectively. Thus the Vlasov term associated with the two-particle distribution function is retained. This kinetic equation is deduced from the kinetic equation in the coherent region obtained by Morita, Mori, and Tokuyama, where the space-time cutoff of the coherent region satisfies _Dbr ₀, _Dt _{c 0}, withr ₀ the Landau length and ₀ the corresponding time scale.