MOLECULAR PHYLOGENETIC ANALYSIS OF MONASCUS FUNGI BASED ON INTERNAL TRANSCRIBED SPACER REGION

A molecular analysis of internal transcribed spacer region has been carried out to reveal the relationship among 16 strains of Monascus spp. A primer set comprised primer ITS1 and ITS4 was used to amplify this region in which they were cloned and scqucnccd. We also compared the sequence result with M. purpureus AF458473, M.ruber AF458470, M. kaoliang AF451859, M. araneous AF458471 and M. pilosus AF451856 and one outgroup species Thermoascus crustaceus U18353. The result showed that 16 Monascus spp. were divided into two large clades while M. ruber AF458470 was basically separated from all those Monascus. One of the two large clades included the seven M. purpureus strains, M. purpureus AF458473, M. araneosus AF458471 and M. kaoliang AF451859. Another large cladc included the six Monascus sp. strains which typically have whitish colonies, the three M. ruber strains and M.pilosus AF451856. However, even outstanding morphological differences possessed by several white Monascus  and one whitish M. purpureus  strain, all Monascus  strains were suggested to be very closely related with similarity >99% almost 100%. Although this ITS analysis could not discriminate cultural and morphological differentiation of Monascus strains studied, yet there is still little genetic variation within these strains. Key words : Molecular genetics/Monascus spp./fung

Molecular Phylogenetic Analysis of Monascus Fungi Based on Internal Transcribed Spacer Region

A molecular analysis of internal transcribed spacer region has been carried out to reveal the relationship among 16 strains of Monascus spp. A primer set comprised primer ITS1 and ITS4 was used to amplify this region in which they were cloned and scqucnccd. We also compared the sequence result with M. purpureus AF458473, M.ruber AF458470, M. kaoliang AF451859, M. araneous AF458471 and M. pilosus AF451856 and one outgroup species Thermoascus crustaceus U18353. The result showed that 16 Monascus spp. were divided into two large clades while M. ruber AF458470 was basically separated from all those Monascus. One of the two large clades included the seven M. purpureus strains, M. purpureus AF458473, M. araneosus AF458471 and M. kaoliang AF451859. Another large cladc included the six Monascus sp. strains which typically have whitish colonies, the three M. ruber strains and M.pilosus AF451856. However, even outstanding morphological differences possessed by several white Monascus and one whitish M. purpureus strain, all Monascus strains were suggested to be very closely related with similarity >99% almost 100%. Although this ITS analysis could not discriminate cultural and morphological differentiation of Monascus strains studied, yet there is still little genetic variation within these strains

A PET Study of Memory for Future Plan

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Measurement of forward neutral pion transverse momentum spectra for s\sqrt{s} = 7TeV proton-proton collisions at LHC

The inclusive production rate of neutral pions in the rapidity range greater than $y=8.9$ has been measured by the Large Hadron Collider forward (LHCf) experiment during LHC $\sqrt{s}=7$\,TeV proton-proton collision operation in early 2010. This paper presents the transverse momentum spectra of the neutral pions. The spectra from two independent LHCf detectors are consistent with each other and serve as a cross check of the data. The transverse momentum spectra are also compared with the predictions of several hadronic interaction models that are often used for high energy particle physics and for modeling ultra-high-energy cosmic-ray showers.Comment: 18 Pages, 10 figures, submitted to Phys. Rev.

Cellular Tropism, Population Dynamics, Host Range and Taxonomic Status of an Aphid Secondary Symbiont, SMLS (Sitobion miscanthi L Type Symbiont)

SMLS (Sitobion miscanthi L type symbiont) is a newly reported aphid secondary symbiont. Phylogenetic evidence from molecular markers indicates that SMLS belongs to the Rickettsiaceae and has a sibling relationship with Orientia tsutsugamushi. A comparative analysis of coxA nucleotide sequences further supports recognition of SMLS as a new genus in the Rickettsiaceae. In situ hybridization reveals that SMLS is housed in both sheath cells and secondary bacteriocytes and it is also detected in aphid hemolymph. The population dynamics of SMLS differ from those of Buchnera aphidicola and titer levels of SMLS increase in older aphids. A survey of 13 other aphids reveals that SMLS only occurs in wheat-associated species