Lamellae expanded after two to three days (Figure 4H), depending

Lamellae expanded after two to three days (Figure 4H), depending on sufficiently high moisture levels, as already observed for other basidiomycetes [17]. The hymenium was enclosed by incurved margins of the pileus, only being exposed when the basidiomata maturated (Figure 4G and 4H). Finally the stipe elongated and the pileus expanded to expose the hymenium for basidiospore liberation (Figure 4I). Basidiomata maturation was regulated by humidity and not all initial primordia progressed to form basidiomata (not shown). Primordia emerged from 75 d after

the exposure of substrate-grown mycelia to water and light in the humid chamber (Figure 1G). The first basidiomata were observed about 10 d after the first primordium was visible, but undifferentiated primordia were PF-02341066 supplier still present on the mat surface when basidiomata appeared. Density of primordia was high, their size not uniform and their production discontinuous, find more suggesting a programmed induction, as in plant inflorescences. The GSK1210151A concentration morphogenesis observed in the initials (Figure 3) resembled

that of other Basidiomycota. Hyphae aggregated towards the surface and assumed a vertical position concurrent with an increase in diameter and compartment length (distance between septa) (Figure 3A and Figure 4A, arrow). These hyphae differentiated to form an agglomerate (Figure 3A) where they converged in an apical group (Figure 3B, #) and two lateral groups, growing in towards the bottom (Figure 3B, black square). A parallel bundle of hyphae with an inclination in direction to the center of the agglomerate was also observed (Figure 3B, *). This bundle diminished in length when the central aggregates increased in size; later, a lateral appendix to the primordium was observed (Figure 3D, arrows and *). Lateral groups (Figure 3D, #)

increased in prominence during development, and the convergent hyphae at the agglomerate apex became vertically Epothilone B (EPO906, Patupilone) prominent (Figure 3D, black squares). The lateral groups tended to bend downwards away from the apex (Figure 3C, *). A group of basal hyphae, however, bent upwards, supporting the hyphal extremity that bent downwards (Figure 3C, arrow and 3D, arrow). As the lateral hyphae expanded, the overlapping of these hyphae diminished (Figure 3E, * and 3F, arrows), increasing the space between these hyphal groups (Figure 3E, arrow). A micrograph of an emerged primordium (Figure 4C) shows a difference in opacity between hyphae, suggesting that a partial digestion led to the spaces between the lamellae. Another freehand section shows the lateral bending of hyphae and the differentiation of the stipe (Figure 4B). This primordium already possessed a differentiated hymenium (not shown). Studies in Agaricus sp. and other edible fungi revealed a hemi-angiocarpous standard developmental stage [17, 19], with a veil covering the primordium. In these fungi, a cluster of parallel and oriented hyphae emerges and forms the stipe and the pileus develops from the apical region.

Bold text indicates statistically significant induction Molecula

Bold text indicates statistically significant induction. Molecular mechanisms of arsenite oxidase transcription The aoxR and aoxS genes encode a two-component system while rpoN encodes a sigma factor which recognizes a particular promoter with a specific -12/-24 binding site. These three proteins may therefore play a role in the initiation of aoxAB transcription. To get further insight 4-Hydroxytamoxifen research buy into the molecular interactions between those regulators and the aoxAB promoter,

we mapped the transcriptional start site of this operon by the amplification of aoxAB cDNA ends and 5′RACE. Messenger RNAs were extracted from induced (1.33 mM As(III)) and non induced H. arsenicoxydans wild-type strain cultures. A single transcriptional start site was identified from induced cells at -26 bp relative to the translation start codon, while no transcriptional start site was identified from non induced cells. In agreement

with this, a TGGCACGCAGTTTGC putative -12/-24 σ54-dependent promoter motif was identified upstream of the aoxAB transcriptional start site (Figure 5). In addition, multiple alignment of aoxAB promoter sequences present in databases buy EPZ5676 revealed a similarity to promoters recognized by σ54 in A. tumefaciens, Thiomonas sp., Rhizobium sp. NT-26, Achromobacter sp., Rhodoferax ferrireducens, Ochrobactrum tritici (Figure 5A). In contrast, no such σ54-dependent promoter motif was found in https://www.selleckchem.com/products/byl719.html several strains containing the aoxAB operon but lacking the two-component transduction system aoxRS operon, such as Chloroflexus aurantiacus,

Chlorobium limicola, Thermus thermophilus, Burkholderia multivorans, Roseobacter litoralis, Pseudomonas sp.TS44, Chlorobium phaeobacteroides and Chloroflexus aggregans (Figure 5B). Figure 5 Determination of aoxA transcription start site by 5′RACE and identification of a σ 54 consensus motif. The transcription start site (TSS) of aoxA is in bold and indicated as +1 in the aoxA promoter sequence. The -12 and -24 boxes are highlighted and the consensus sequence is indicated in Glutathione peroxidase bold. The aoxA promoter was also aligned with the promoter sequences of A. tumefaciens, Thiomonas sp., Rhizobium sp. NT-26, Achromobacter sp., R. ferrireducens, O. tritici, C. aurantiacus, C. limicola, T. thermophilus, B. multivorans, R. litoralis, Pseudomonas sp.TS44, C. phaeobacteroides and C. aggregans. Two distincts sequences were shown A. DNA sequences with a σ54-dependent promoter motif (indicated in boxes). B. DNA sequences without a σ54-dependent promoter motif. Sequence informations of other genes were obtained from GenBank database and their localization on the chromosome or the plasmid is given by a nucleotide numbering. Their accession numbers are: A. tumefaciens (ABB51929.1), Thiomonas sp. (ABY19317.1), Rhizobium sp. NT-26 (AAR05655.1), Achromobacter sp. (ABP63659.1), R. ferrireducens (YP_524326.1), O. tritici (ACK38266.1), C. aurantiacus (YP_001634828.1), C. limicola (YP_001942455.1), T. thermophilus (YP_145367.1), B.

CrossRef 67 Cole J, Wang Q, Cardenas E,

Fish J, Chai B,

CrossRef 67. Cole J, Wang Q, Cardenas E,

Fish J, Chai B, Farris R, Kulam-Syed-Mohideen A, McGarrell D, Marsh T, Garrity G: The ribosomal database project: improved alignments and new tools for rRNA analysis. Nucleic Acids Res 2009,37(1):D141-D145.PubMedCrossRef 68. Parks DH, Beiko RG: Identifying biologically relevant differences between metagenomic communities. Bioinformatics 2010,26(6):715–721.PubMedCrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions DGW and NS equally contributed to this work by conceiving, designing and coordinating the study, by carrying out sampling and molecular biology investigations, by leading the development of the PyroTRF-ID bioinformatics methodology, by analyzing all collected data, and by drafting the manuscript. DGW additionally conceived the tables and the figures. LS was responsible for the optimization and validation of PyroTRF-ID https://www.selleckchem.com/products/nvp-bsk805.html and wrote the underlying codes. GL coded the initial bioinformatics procedure. JM and PR participated in the design of the study. JR coordinated the development of PyroTRF-ID at the Bioinformatics and Biostatistics Core Facility. CH led the project and gave the initial idea of reconstructing

T-RFLP profiles from pyrosequencing data. DGW and NS wrote the manuscript, with additional contributions of JM, PR, and CH. All authors read and approved the click here final manuscript.”
“Background Viruses in the genus Alphavirus belong to the group IV Togaviridae family and include nearly 30 virus species [1]. Alphaviruses are able to infect humans and various vertebrates via arthropods, such as mosquitoes. The 11–12 kb Alphavirus genome is a single-stranded positive during sense RNA flanked by a 5’ terminal cap and 3’ poly-A tail, and composed of four non-structural proteins genes (nsP1 to nsP4) and five structural proteins gene (C (nucleocapsid),

E3, E2, 6 K, and E1 proteins) [2]. Getah virus (GETV) is a mosquito-borne enveloped RNA virus belonging to the Semliki Forest virus (SFV) complex in the genus Alphavirus[1]. To date, 10 strains of GETV have been isolated in China: M1, HB0234, HB0215-3, YN0540, YN0542, SH05-6, SH05-15–17 and RG7112 GS10-2 [3]. GETV has been shown to cause illnesses in humans and livestock animals and antibodies to GETV have been detected in many animal species worldwide [4–6]. The identification of novel virus species is important for the identification and characterization of disease. However, present research methods are mostly applicable for known viruses but few methods exist to characterize unknown viruses. Current molecular biological techniques for the identification of new virus species are troublesome since some viruses do not replicate in vitro but some may cause a cytopathic effect. Furthermore, specific techniques that require sequence identification are not applicable.

CrossRef 32 Hafiz MM, El-Shazly O, Kinawy N: Reversible phase ch

CrossRef 32. Hafiz MM, El-Shazly O, Kinawy N: Reversible phase change in Bi x Se 100-x chalcogenide thin films for using as optical recording Selleck Y-27632 medium. Appl Surf Sci 2001, 171:231–241.CrossRef 33. Zhao J, Liu H, Ehm L, Dong D, Chen Z, Gu G: High-pressure GSK3235025 phase transitions, amorphization, and crystallization behaviors in Bi 2 Se 3 . J Phys Condens Matter 2013, 25:125602.CrossRef 34. EM Explorer http://​www.​emexplorer.​net/​ 35. Johnson PB, Christy RW: Optical constants of the noble metals. Phys Rev B 1972, 6:4370–4379.CrossRef 36. Berenger JP: Three-dimensional perfectly matched

layer for the absorption of electromagnetic waves. J Comput Phys 1996, 127:363–379.CrossRef 37. Born M, Wolf E, Bhatia AB: Principles of Optics. Cambridge: Cambridge University Press; 1997:61–70. 38. Nicolson AM, Ross GF: Measurement of the intrinsic properties of materials by time-domain techniques. IEEE Trans Instrum Meas 1970, 19:377–382.CrossRef 39. Smith DR, Schultz S, Markos P, Soukoulis CM:

Determination of effective permittivity and permeability of metamaterials from reflection and transmission coefficients. Phys Rev B 2002, 65:195104.CrossRef 40. Chen XD, Grzegorczyk TM, Wu B, Pacheco JJ, Kong JA: Robust method to retrieve the constitutive effective parameters of metamaterials. Phys Rev E 2004, 70:016608.CrossRef 41. Zhang S, Fan W, Malloy click here KJ, Brueck SRJ: Near-infrared double negative metamaterials. Opt Express 2005, 13:4922–4930.CrossRef 42. Ortuño R, García-Meca Carbohydrate C, Rodríguez-Fortuño FJ, Martí J, Martínez A: Role of surface plasmon polaritons on optical transmission through double layer metallic hole arrays. Phys Rev B 2009, 79:075425.CrossRef Competing interests The authors declare that they have no competing interests. Authors’ contributions TC conceived the idea of using topological insulator for tuning the resonance in the metamaterials, designed the

metamaterial, and wrote the manuscript. SW carried out the simulations and prepared the figures. Both authors read and approved the final manuscript.”
“Background Recently, nanoscale particles have drawn increasing attention. For example, gold particles, as a popular nanomaterial with outstanding optoelectronic properties, have been widely used in sensor applications by the enrichment of detection range and optimization and enhancement of sensitivity [1–4]. In addition, Au particles are also attractive based on their capacity to catalyze one-dimensional (1-D) nanostructures, namely nanopillars and nanowires with lots of remarkable properties via various epitaxial growth mechanisms [5–10]. Fabrications of diverse nanowires such as GaN, ZnO, InAs, GaAs, Si, and Ge have been demonstrated using Au droplets as catalyst [11–18]. Nonetheless, given the wide range of substrates utilized, Au droplets can be successfully utilized in the fabrication of the various nanowires and many elements utilized for substrates would diffuse into gold during the fabrications of nanowires [11–18].

Cutoffs of 99% and 94%

Cutoffs of 99% and 94% selleck compound were established for species classification for 16S and recA analyses, respectively (data not shown). We identified 23 B. mallei, 4 B. oklahomensis, 12 B. thailandensis, 5 B. thailandensis-like species,

44 B. ubonensis, and 25 unidentified Burkholderia species strains. LPS genotyping (PCR) Eleven out of 12 B. thailandensis strains had the LPS AZD2281 manufacturer genotype A. All 23 tested B. mallei strains also had the LPS genotype A. LPS genotype B was detected in 11 out of 44 strains of B. ubonensis. We note that these LPS genotype B strains were all of Australian origin. LPS genotype B2 was found in B. thailandensis strain 82172, and B. thailandensis-like species strains MSMB121, MSMB122, MSMB712, and MSMB714. This is the first reported incidence of another O-antigen in B. thailandensis while B. thailandensis-like MSMB121 was previously described as expressing this type [11]. No other species was positive for type A, B, or B2 (Table 1 and Additional file 1: Table S1). Table 1 Prevalence of four B. pseudomallei O-antigen types in near-neighbors

Species Total strains tested Known B. pseudomallei O-antigen     Type A Type B Type B2 Rough Type B. mallei 23 21 0 0 2 B. oklahomensis 4 1 0 0 0 B. thailandensis 12 11 0 1† 0 B. thailandensis-like 5 0 0 4 0 B. cepacia 2 0 0 0 0 B. multivorans 3 0 0 0 0 B. ubonensis 44 0 11 1‡ 0 B. vietnamiensis 1 0 0 0 0 Unidentified Burkholderia spp. 19 0 0 1* www.selleckchem.com/products/chir-99021-ct99021-hcl.html 0 †Strain 82172, collected from French Methane monooxygenase foal. ‡Strain MSMB108, collected from Northern Australian environment. *Strain MSMB175, a soil strain collected from Australia. This strain is currently being proposed as a new Burkholderia species. LPS phenotyping (SDS-PAGE, silver staining and immunoblotting) We identified LPS banding patterns in all tested bacterial strains by comparing them with known LPS banding patterns A, B, and B2 in reference B. pseudomallei strains (Additional file 2: Figure S1). Previously, only type A O-antigen has been described in B. thailandensis[11, 12]. Eleven out of 12 tested strains expressed a type A banding pattern consistent with the PCR results.

We note that B. thailandensis strain 82172 had the LPS genotype B2 via PCR, which was confirmed as serotype B by immunoblotting (Figure 1). B. pseudomallei strains expressing type B2 have previously been isolated only in Australia and Papua New Guinea, while this B. thailandensis strain was isolated in France [11, 18]. Additionally, type A was recently described in B. oklahomensis E0147 [11], whereas the remaining three B. oklahomensis strains isolated from Oklahoma [19] displayed an unknown non-seroreactive ladder pattern (not shown in Figure 1). Figure 1 Serotype A (a) and B (b) western blots. Lane 1 – B. pseudomallei K96243, 2 – B. thailandensis E264, 3 – B. oklahomensis E0147, 4 – B. pseudomallei 576, 5 – B.

First, one can suggest that this allele has been inactivated or i

First, one can suggest that this allele has been inactivated or importantly down regulated in the CI-inducing strains of isopods. Change in regulatory element repertoire and divergence in patterns of expression

may occur after small-scale duplication of the genome [36]. A corollary to a change in location, paralogous and homologous pk2 copies within and among Wolbachia strains would have followed different evolutionary trajectories leading to such a phenotypic diversity. Second, genomic imprinting, process by which genes are expressed from only one parental allele due to epigenetic mechanism, can be considered as a molecular mechanism underlying the diversity of phenotypes. Recently, early changes in gene imprinting and aberrant expression of specific genes have

been shown to be coupled to parthenogenesis in mice embryos [37]. Third, one AC220 datasheet can suggest that genes in the pk2 family could have diverse functions. In this way, BIX 1294 post-transcriptional modifications and dosage of Wolbachia products, as well as genetic control by the host, cannot be dismissed. As previously suggested [38], Selleckchem FHPI differences in Wolbachia-induced feminization as well as the presence of the bacteria in O. asellus males, may simply result from differences in bacterial dosage or in host targets. The basic molecular mechanisms that mediate Wolbachia feminization are also still unknown

although it is unlikely that this effect is driven by only one gene. In A. vulgare Wolbachia effectors may target the proteinaceous androgenic hormone or its receptor, or another major sex determinant, thereby inhibiting the androgenic gland differentiation and preventing the androgenic hormone from reaching the target tissues such as gonads and tegumental epithelium [2, 39, 40]. This hypothesis suggests a late action of feminizing Wolbachia on host target(s) during its development, as opposed to the very early action of other Wolbachia strains that induce parthenogenesis, CI or male killing [5, 41]. Conclusions Our results highlight a large copy number variation of both pk1 and pk2 genes among strains, likely Tolmetin linked to prophage diversity, and also the specific expression of one pk2 allele only in the feminizing Wolbachia strains of isopods. This correlation supports the hypothesis that phenotype-related effectors or specific strain determinants in Wolbachia are likely to be encoded by prophage genes, ankyrin-repeat encoding genes, and predicted genes of unknown function [42]. Our results thus reveal the need to search for host molecules targeted by Wolbachia ankyrins and their functions with respect to host sex manipulation by Wolbachia. Methods Wolbachia-infected isopod species All isopods used in this study were collected in France and reared in the laboratory.

Zhang J, Yang Y, Teng D, Tian Z, Wang S, Wang J: Expression of pl

Zhang J, Yang Y, Teng D, Tian Z, Wang S, Wang J: Expression of plectasin in Pichia pastoris and its characterization as a new antimicrobial peptide against Staphyloccocus and Streptococcus . Protein Expr Purif 2011, 78:189–196.PubMedCrossRef 31. Zhang Y, Teng D, Mao R, Wang X, Xi D, Hu X, Wang J: High expression Y-27632 purchase of a plectasin-derived peptide NZ2114 in Pichia pastoris and its pharmacodynamics,

postantibiotic and synergy against Staphylococcus aureus . Appl Microbiol Biotechnol 2014, 98:681–694.PubMedCrossRef 32. Mao R, Teng D, Wang X, Xi D, Zhang Y, Hu X, Yang Y, Wang J: Design, expression, and characterization of a novel targeted plectasin against methicillin-resistant Staphylococcus aureus . Appl Microbiol Biotechnol 2013, 97:3991–4002.PubMedCrossRef 33. Richard C, Drider D, Elmorjani K, Marion D, Prévost

H: Heterologous expression and purification of active Divercin V41, a Class IIa bacteriocin encoded by a synthetic gene in Escherichia coli . J Bacteriol 2004, 186:4276–4284.PubMedCrossRefPubMedCentral 34. Casaus P, Nilsen T, Cintas LM, Nes IF, Hernández PE, Holo H: Enterocin B, a new bacteriocin from Enterococcus faecium T136 which can act synergistically with enterocin A. Microbiology 1997, 143:2287–2294.PubMedCrossRef 35. Kaur K, Andrew LC, Wishart DS, Vederas JC: Dynamic relationships among type IIa bacteriocins: temperature effects on antimicrobial activity ML323 cost and on structure of the C-terminal amphipathic α helix as a receptor-binding region. Biochemistry 2004, 43:9009–9020.PubMedCrossRef 36. Jack RW, Wan J, Gordon J, Harmark

K, Davidson BE, Hillier AJ, Wettenhall R, Hickey MW, Coventry MJ: Characterization of the ATM/ATR mutation chemical and antimicrobial properties of piscicolin 126, a bacteriocin produced by Carnobacterium piscicola JG126. Appl Environ Microbiol 1996, 62:2897–2903.PubMedPubMedCentral 37. Rehaiem A, Guerra NP, Belgacem ZB, Bernárdez PF, Castro LP, Manai M: Enhancement of enterocin A production by Enterococcus faecium Dynein MMRA and determination of its stability to temperature and pH. Biochem Eng J 2011, 56:94–106.CrossRef 38. Yamada O, Sakamoto K, Tominaga M, Nakayama T, Koseki T, Fujita A, Akita O: Cloning and heterologous expression of the antibiotic peptide (ABP) genes from Rhizopus oligosporus NBRC 8631. Biosci Biotechnol Biochem 2005, 69:477–482.PubMedCrossRef 39. Gänzle MG, Weber S, Hammes WP: Effect of ecological factors on the inhibitory spectrum and activity of bacteriocins. Int J Food Microbiol 1999, 46:207–217.PubMedCrossRef 40. Reenen V: Isolation, purification and partial characterization of plantaricin 423, a bacteriocin produced by Lactobacillus plantarum . J Appl Microbiol 1998, 84:1131–1137.PubMedCrossRef 41. Rodriguez JM, Martinez MI, Kok J: Pediocin PA-1, a wide-spectrum bacteriocin from lactic acid bacteria. Crit Rev Food Sci Nutr 2002, 42:91–121.PubMedCrossRef 42.

Interestingly, region I in strain Beluga differed from both CDC66

Sepantronium research buy Interestingly, region I in strain Beluga differed from both CDC66177 and Alaska E43 while region II was identical to that found in Alaska E43. While the mechanism of toxin gene cluster insertion into the rarA operon is unclear, the sequence similarity in region II between strains Beluga and Alaska E43 suggests at least a partial similarity in the origin of Linsitinib purchase the recombination event that results in the insertion of the toxin gene cluster. However, strain CDC66177 lacks similarity to either strain Beluga or Alaska E43 at either region suggesting that the recombination event resulting in the insertion of the toxin gene cluster in strain CDC66177

originated differently compared to strains Beluga or Alaska E43. Analysis of the genome sequence data explains the unexpected ~1.7 kb band hybridized by the rarA probe in strain CDC66177. The presence of an XbaI site XMU-MP-1 clinical trial within the toxin gene cluster of both CDC66177 and Alaska E43 and an additional site downstream of the larger rarA fragment in strain CDC66177 yield an ~1.7 kb fragment. Notably the genome sequence of strain 17B also demonstrates the presence of a XbaI site downstream of the intact rarA gene. Similar to other type E toxin gene clusters, strain CDC66177 contains an intact rarA gene that

does not hybridize the rarA probe used in our studies. BLAST analysis of this gene demonstrated 98% nucleotide similarity with the gene present in Alaska E43. Since the bont/E gene in strain CDC66177 displayed significant

divergence compared to other reported bont/E genes, we compared the nucleotide sequences of the remaining toxin gene cluster components (ntnh, p47, orfX1-3) to those found in Alaska E43 and Beluga (Table 1). While these genes are nearly identical in Alaska E43 nearly and Beluga, the genes in CDC66177 ranged from 88.2-96.9% nucleotide identity compared to those in Alaska E43 and/or Beluga. Table 1 Pairwise alignment of toxin gene cluster components Gene % Nucleotide Identity Alaska E43/CDC66177 Beluga E/CDC66177 Alaska E43/Beluga E orfX3 94.9 94.9 100 orfX2 91.1 91.1 99.5 orfX1 94.9 94.9 100 p47 88.2 88.2 100 ntnh 96.8 96.9 99.9 bont/E 93.9 94.1 99.3 In order to further investigate the genomic sequence of strain CDC66177, the average nucleotide identity (ANI) of this strain was compared to Alaska E43 and Beluga. Briefly, 1,020 nucleotide fragments of the query genome were compared to the subject genome using BLAST to determine the ANI value [17]. Richter and Rosselló-Móra [17] proposed an ANI of 95-96% as the boundary of considering two genomes as belonging to a single bacterial species. While comparison of the genomes of strains Alaska E43 and Beluga resulted in an ANI > 97%, comparison of strain CDC66177 with Alaska E43 and Beluga resulted in ANI values between 93-94% (Table 2). Interestingly, comparison of strain CDC66177 with 17B displayed > 98% ANI while comparison of either Alaska E43 or Beluga with 17B resulted in ANI values < 94%.

Photosynth Res 13:99–100CrossRef Gerhart D (1996) Forty-five year

Photosynth Res 13:99–100CrossRef Gerhart D (1996) Forty-five years of developmental

biology of photosynthetic bacteria. Photosynth Res 48(3):325–352CrossRef Gest H (1988) Sun-beams, cucumbers, and purple bacteria. Historical milestones in early studies of photosynthesis revisited. Photosynth Res 19(3):287–308 Gest H (1991) The legacy of Hans Molisch (1856–1937), photosynthesis savant. Photosynth Res 30(1):49–59 Gest H (1993) History of concepts of the comparative biochemist of oxygenic and anoxygenic photosyntheses. Photosynth Res 35(1):87–96CrossRef Gest H (1994) A microbiologist’s odyssey: bacterial viruses to photosynthetic bacteria. Photosynth Res 40(2):129–146CrossRef Gest H (1994) Discovery of the heliobacteria. Photosynth Res 41(1):17–21CrossRef selleck Gest H (1997) A misplaced chapter in the history of photosynthesis research. The second publication (1796) on plant processes by Dr. Jan Ingen-Housz, MD, discoverer of photosynthesis. Photosynth Res 53:65–72CrossRef Gest H (1999) Memoir of a 1949 railway journey with photosynthetic bacteria. Photosynth

Res 61(1):91–96CrossRef Gest H (2000) Bicentenary homage to C188-9 research buy Dr Jan Ingen-Housz, MD (1730–1799), pioneer of photosynthesis research. Photosynth Res 63(2):183–190PubMedCrossRef Gest H (2000) Bicentenary homage to Jan Ingen-Housz, pioneer of photosynthesis research. Photosynth Res 63:183–190PubMedCrossRef Gest H (2002) History of the word photosynthesis

and evolution of its definition. Photosynth Res 73(1–3):7–10PubMedCrossRef Gest H (2002) Photosynthesis and phage: early studies on phosphorus metabolism in photosynthetic microorganisms with 32p, and how they led to the serendipic discovery of 32p-decay suicide of bacteriophage. Photosynth Res 74(3):331–PARP cancer 339PubMedCrossRef Gest H (2004) Samuel Ruben’s contributions to research on photosynthesis and bacterial metabolism with radioactive carbon. not Photosynth Res 80(1–3):77–83PubMedCrossRef Gest H, Blankenship RE (2004) Time line of discoveries: anoxygenic bacterial photosynthesis. Photosynth Res 80(1–3):59–70PubMedCrossRef Ghosh AK (2004) Passage of a young Indian physical chemist through the world of photosynthesis research at Urbana, Illinois, in the 1960s: a personal essay. Photosynth Res 80(1–3):427–437PubMedCrossRef Giacometti GM, Giacometti G (2006) Twenty years of biophysics of photosynthesis in Padova, Italy (1984–2005): a tale of two brothers. Photosynth Res 88(3):241–258PubMedCrossRef Gibbs M (1999) Educator and editor. Annu Rev Plant Physiol Plant Mol Biol 50:1–25PubMedCrossRef Good NE (1986) Confessions of a habitual skeptic. Annu Rev Plant Physiol 37:1–22CrossRef Goodwin J (1992) Dr Robin Hill: natural dyes. Photosynth Res 34(3):321–322CrossRef Gorham PR, Nozzolillo CG (2006) Photosynthesis research in Canada from 1945 to the early 1970s.

Biochim Biophys Acta Bioenerg 1807(4):437–443 doi:10 ​1016/​j ​b

Biochim Biophys Acta Bioenerg 1807(4):437–443. doi:10.​1016/​j.​bbabio.​2011.​01.​007 CrossRef Ratnala VRP, Kiihne SR, Buda F, Leurs R, de Groot HJM, Degrip WJ (2007) Solid-state NMR evidence for a protonation switch in the binding pocket of the H1 receptor upon binding of the agonist histamine. J Am Chem Soc 129(4):867–872. doi:10.​1021/​ja0652262 PubMedCrossRef Renault M, Cukkemane A, Baldus M (2010) Solid-state NMR spectroscopy

on complex biomolecules. Angew Chem Int Ed 49(45):8346–8357. doi:10.​1002/​anie.​201002823 CrossRef Roszak AW, Howard TD, Southall J, Gardiner AT, Law CJ, Isaacs NW, Cogdell RJ (2003) Crystal structure of the RC-LH1 core complex from Rhodopseudomonas palustris. Science 302(5652):1969–1972. doi:10.​1126/​science.​AR-13324 1088892 eFT-508 mw BI 10773 chemical structure PubMedCrossRef Ruban AV, Berera R, Ilioaia C, van Stokkum IHM, Kennis JTM, Pascal AA, van Amerongen H, Robert B, Horton P, van Grondelle R (2007) Identification of a mechanism of photoprotective energy dissipation in higher plants. Nature 450 (7169):575–578. doi:10.​1038/​nature06262 Schulten EAM, Matysik J, Alia, Kiihne S, Raap J, Lugtenburg J, Gast P, Hoff AJ, de

Groot HJM (2002) (13)C MAS NMR and photo-CIDNP reveal a pronounced asymmetry in the electronic ground state of the special pair of Rhodobacter sphaeroides reaction centers. Biochemistry 41 (27):8708–8717 Shimada Y, Wang ZY, Mochizuki Y, Kobayashi M, Nozawa T (2004) Functional expression and characterization of a bacterial light-harvesting membrane protein in Escherichia coli and cell-free synthesis systems. Biosci Biotechnol Biochem 68(9):1942–1948PubMedCrossRef Standfuss R, van Scheltinga ACT, Lamborghini M, Kuhlbrandt

W (2005) Mechanisms of photoprotection and nonphotochemical quenching in pea light-harvesting complex at 2.5A resolution. EMBO J 24(5):919–928. doi:10.​1038/​sj.​emboj.​7600585 PubMedCrossRef van Gammeren AJ, Hulsbergen FB, Hollander JG, de Groot HJM (2004) Biosynthetic site-specific C-13 labeling of the light-harvesting 2 protein complex: a model for solid state NMR structure determination of transmembrane proteins. J Biomol NMR 30(3):267–274. doi:10.​1007/​s10858-004-3736-7 PubMedCrossRef van Gammeren Buspirone HCl AJ, Buda F, Hulsbergen FB, Kiihne S, Hollander JG, Egorova-Zachernyuk TA, Fraser NJ, Cogdell RJ, de Groot HJM (2005a) Selective chemical shift assignment of B800 and B850 bacteriochlorophylls in uniformly [C-13, N-15]-labeled light-harvesting complexes by solid-state NMR spectroscopy at ultra-high magnetic field. J Am Chem Soc 127(9):3213–3219. doi:10.​1021/​ja044215a PubMedCrossRef van Gammeren AJ, Hulsbergen FB, Hollander JG, de Groot HJM (2005b) Residual backbone and side-chain C-13 and N-15 resonance assignments of the intrinsic transmembrane light-harvesting 2 protein complex by solid-state magic angle spinning NMR spectroscopy.