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Notes: We report the results of an experimental study on efficient laser action in an optically pumped GaN/AlGaN separate-confinement heterostructure (SCH) in the temperature range of 10–300 K. The lasing threshold was measured to be as low as 15 kW/cm2 at 10 K and 105 kW/cm2 at room temperature. Strongly polarized (TE:TM≥300:1) lasing peaks were observed over the wavelength range of 358–367 nm. We found high-finesse lasing modes that originate from self-formed microcavities in the AlGaN and GaN layers. Through analysis of the relative shift between spontaneous emission and lasing peaks, combined with the temperature dependence of the lasing threshold, we conclude that exciton–exciton scattering is the dominant gain mechanism leading to low-threshold ultraviolet lasing in the GaN/AlGaN SCH over the entire temperature range studied. Based on our results, we discuss possibilities for the development of ultraviolet laser diodes with a GaN active medium. © 1999 American Institute of Physics.

Notes: We investigated the effects of well thickness on spontaneous and stimulated emission (SE) in GaN/AlGaN separate confinement heterostructures (SCHs), grown by low-pressure metalorganic chemical vapor deposition. The SCH wells are unstrained and lattice-matched to a GaN buffer layer. Our series of SCHs had GaN well thicknesses of 3, 5, 9, and 15 nm. We explain the spontaneous emission peak energy positions of the SCHs in terms of spontaneous and strain-induced piezoelectric polarizations. At 10 K, the carrier lifetime was found to be lowest for a 3 nm well, and the SE threshold was lowest for a 5 nm well. We show that the screening of the piezoelectric field and the electron-hole separation are strongly dependent on the well thickness and have a profound effect on the optical properties of the GaN/AlGaN SCHs. The implications of this study on the development of near- and deep-ultraviolet light emitters are discussed. © 2001 American Institute of Physics.

Notes: We report the results of an experimental study of the stimulated emission (SE) properties of AlGaN epilayers grown by metalorganic chemical vapor deposition under high optical excitation conditions in the temperature range of 30–300 K. The band gap and energy position of spontaneous and SE peaks were measured over the entire temperature range studied. Through an analysis of the temperature dependence of the relative energy positions and the SE threshold, combined with absorption and time-resolved photoluminescence measurements, we estimated the carrier density at threshold to be ∼1019 cm−3 throughout the temperature range studied. Such a high carrier density indicates that an electron-hole plasma is responsible for the generation of gain in this material system from 30 to 300 K. Issues related to the development of short-wavelength AlGaN-based light emitting devices are discussed. © 2000 American Institute of Physics.

Notes: The homes of 120 patients with asthma, 57 in Vancouver and 63 in Winnipeg, were studied. The characteristics of the homes were assessed by a questionnaire. Dust samples were collected and the indoor relative humidity was measured four times during the year covering all four seasons in both cities. Mite allergen levels were determined using monoclonal antibodies against Der p I and Der f I by the ELISA method. The mean levels of both mite allergens in mattress and floor samples in the homes in Vancouver and in Winnipeg were relatively low for all seasons. Mite allergen levels were found to be associated with city, season and individual home differences. They were significantly higher in Vancouver than in Winnipeg. Der p I and Der f I in mattress samples in both cities and Der f I in floor samples in Vancouver, varied by season. The indoor relative humidity level in the homes in Vancouver were also significantly higher than those in Winnipeg. There was, however, no significant association between the levels of indoor relative humidity and the levels of mite allergens after adjusting for variations in city, season and individual home. Although individual home differences were highly associated with mite allergen levels, only a few home characteristics were found to be related to mite allergen levels such as the type and the age of the home, the type of heating, the use of feather pillows and the number of occupants in the homes. Whether low levels of mite allergens are partially responsible for the relatively low prevalence of childhood asthma in Canada remains to be investigated.

Notes: Polyacetylenes and their thiophene derivatives were tested for their effects on human skin. Topically applied α-terthienyl evoked bi-phasic phototoxic dermatitis and the appearance of ‘sunburn’ cells in human epidermis. None of 11 polyacetylenes had the same effect although they mimicked α-terthienyl in their phototoxic effects on Candida albicans and certain pathogenic microorganisms. The UV-mediated antibiotic activity of the compounds and their apparent lack of phototoxicity towards the skin suggest a potential topical therapeutic role for them in yeast, fungal and bacterial infections and light-responsive dermatoses. Their topical sensitizing capacity, however, has not yet been studied.

Notes: Pseudomonas aeruginosa co-expresses A-band lipopolysaccharide (LPS), a homopolymer of rhamnose, and B-band LPS, a heteropolymer with a repeating unit of 2–5 sugars which is the serotype-specific antigen. The gene clusters for A- and B-band biosynthesis in P. aeruginosa O5 (strain PAO1) have been cloned previously. Here we report the DNA sequence and molecular analysis of the B-band O-antigen biosynthetic cluster. Sixteen open reading frames (ORFs) thought to be involved in synthesis of the O5 O antigen were identified, including wzz (rol), wzy (rfc), and wbpA–wbpN. A further 3 ORFs not thought to be involved with LPS synthesis were identified (hisH, hisF, and uvrB). Most of the wbp genes are found only in serotypes O2, O5, O16, O18, and O20, which form a chemically and structurally related O-antigen serogroup. In contrast, wbpM and wbpN are common to all 20 serotypes of P. aeruginosa. Although wbpM is not serogroup-specific, knockout mutations confirmed it is necessary for O5 O-antigen biosynthesis. A novel insertion sequence, IS1209, is present at the junction between the serogroup-specific and non-specific regions. We have predicted the functions of the proteins encoded in the wbp cluster based on their homologies to those in the databases, and provide a proposed pathway of P. aeruginosa O5 O-antigen biosynthesis.

Notes: Pseudomonas aeruginosa can express two distinct forms of lipopolysaccharide (LPS), called A-band and B-band. As an attempt to understand the molecular biology of the synthesis and regulation of these LPS antigens, a recombinant plasmid, pFV3, containing genes for A-band expression was isolated previously. In the present study, P. aeruginosa strain PAO1 was mutagenized with transposon Tn5-751 and yielded a B-band-deficient mutant, called ge6. This mutant was mated with a PAO1 genomic library, and transconjugants were screened for complementation of B-band using B-band-specific monoclonal antibody MF15-4. Recombinant plasmid pFV100 was subsequently isolated by its ability to complement B-band expression in ge6. SDS-PAGE analysis of LPS from ge6 and ge6(pFV100) revealed that ge6 was deficient in expression of B-band, while ge6(pFV100) had an LPS profile similar to that of the parent strain PA01. With A-band and B-band genes cloned in separate plasmids, pFV3 and pFV100 respectively, we were able to determine the map location of these LPS genes on the P. aeruginosa PAO1 chromosome using pulsed-field gel electrophoresis. A-band genes mapped at 5.75 to 5.89 Mbp (Spel fragment SpK; Dpnl fragment DpF2), while genes involved with expression of B-band LPS mapped at 1.9 Mbp (Spel fragments SpC, Spl and SpAl; Dpnl fragment DpD) on the 5.9 Mbp chromosome. We also performed initial characterization of a gene involved with synthesis of A-band present on pFV3. We previously reported that recombinant plasmid pFV3 and subcloned plasmid pFV36 complemented A-band synthesis in rd7513, an A− mutant derived from A+ strain AK1401. pFV36 was mutagenized with transposon Tn1000 to reveal a one-kilobase region capable of complementing the expression of A-band in the A− strain rd7513. This region was subcloned as a 1.6 kb Kpnl fragment into plasmid vector pAK1900 and the resulting clone named pFV39. Labelling of proteins encoded by pAK1900 and pFV39 in Escherichia coli maxicells revealed a single unique polypeptide of approximately 37kDa expressed by pFV39. Supernatants from disrupted cells of rd7513(pFV39) and AK1401 converted 14C-labelled-guanosine diphospho (GDP)-D-mannose to GDP-rhamnose, while supernatants from rd7513 did not show synthesis of GDP-rhamnose. The data therefore suggest that conversion of GDP-D-mannose to GDP-rhamnose is required for synthesis of A-band LPS, and that a 37kDa protein is involved in this conversion.