QM基因研究进展

对QM基因的研究进展做了综述,希望为深入开展不同物种QM基因功能研究提供一些参考。     

胨冻样芽孢杆菌(Bacillus mucilaginosus YNUCC0001)絮凝剂生产、絮凝特性及其系统发育学分析

对BacillusmucilaginosusYNUCC000116SrDNA的1481bp片段与GenBank中最相似的16个分类单位进行了比较。UPGMA,NJ,ME和MP方法构建的系统发育树显示B.mucilaginosusYNUCC0001与B.mucilaginosusHSCC1605T、B.mucilaginosus1480D及Paenibacillussp.NBT形成一个单系群分支。在50L全自动发酵罐中30℃发酵52h后,菌株YNUCC0001产生的胞外生物多聚絮凝剂(EBF)达到最大产率(粘度:3420C.P.)。在pH4.0、用量为0.25mlL-1的条件下,这种EBF对高岭土悬浊液的絮凝活性最大(99.8%);121℃高压灭菌60min后絮凝活性维持在98.6%。Hg2 ,Ca2 ,Mg2 ,K ,Zn2 对其絮凝活性有促进作用,而Fe3 、Al3 、EDTA和Cu2 则有强烈抑制。     

Extensive chromosome translocation in a clinical isolate showing the distinctive carbohydrate assimilation profile from a candidiasis patient

Variation of the electrophoretic karyotype is common among clinical strains of Candida albicans and chromosome translocation is considered one of the causes of karyotypic variation. Such chromosome translocations may be a mechanism to confer phenotypic diversity on the imperfect fungus C. albicans. A clinical strain, TCH23, from a vaginal candidiasis patient shows distinct carbohydrate assimilation profile, serotype B, no chlamydospore formation and an atypical karyotype (Asakura et al., 1991). To examine the taxonomic relationship among C. albicans, Candida dubliniensis and this strain, we sequenced the internal transcribed spacer 1 (ITS1) of nuclear ribosomal DNA. The ITS1 sequence of TCH23 was identical with that of C. albicans but not of C. dubliniensis. Thus, strain TCH23 was classified as a variant of C. albicans with an atypical phenotype. The chromosomal DNAs of this strain were resolved into 13 bands on pulse-field gel electrophoresis (PFGE). Using DNA probes located at or near both ends of each chromosome of C. albicans, we investigated the chromosome organization of this strain. Referring to the SfiI map of C. albicans 1006 (Chu et al., 1993), we found that seven chromosomal DNA bands in strain TCH23 were reciprocal chromosome translocations. One homologue from chromosomes 1, 2 and 6 and both homologues from chromosomes 4 and 7 participated in these events. One translocation product was composed of three SfiI fragments, one each from chromosomes 2, 4 and 7. We deduced the breakpoints of chromosome translocation from the physical map of this strain; between 1J and 1J1, between 2A and 2U, both ends of 4F2, between 6C and 6O and both ends of 7F.     

Characterization of microbial communities in a fluidized-pellet-bed bioreactor for wastewater treatment

In order to make clear the microbiological characteristics of the fluidized-pellet-bed bioreactor (FPB) which is a newly developed wastewater treatment device to perform coagulation, particle pelletization, biological degradation and solid-liquid separation in a single unit, the method of denaturing gradient gel electrophoresis (DGGE) was applied in this study paying attention to the microbial diversity of the granular sludge. Spread plate method was also used for enumeration of aerobic bacteria in unit weight of granular sludge. As a result, slight difference was found between the total aerobic bacteria at the bottom, middle, and top sections though the dissolved oxygen (DO) concentration decreased from about 3.5 mg/L at the bottom inlet to 0.23 mg/L at the top of the FPB bioreactor. From the DGGE finger printing, 17 common species were identified from all these sections, and certain specific species were also identified from each section. The comparability of the microbial communities in the three sections was 83.1%, indicating a very stable structure of the microbial communities. The 16 S rRNA sequence analysis results revealed that the 18 operational taxonomic units (OTUs) obtained all belong to Eubacteria. Among them 11 are Proteobacteria, 3 are Actinobacteria, 2 are low G + C gram-positive bacteria and the remaining 2 belong to other bacteria branches. The dominant microbial communities are typical aerobes or facultative anaerobes commonly encountered in conventional activated sludge.     

Ribosomal Synthesis of Natural‐Product‐Like Bicyclic Peptides in Escherichia coli

Methods to access natural‐product‐like macrocyclic peptides can disclose new opportunities for the exploration of this important structural class for chemical biology and drug discovery applications. Here, the scope and mechanism of a novel strategy for directing the biosynthesis of thioether‐bridged bicyclic peptides in bacterial cells was investigated. This method entails split intein‐catalyzed head‐to‐tail cyclization of a ribosomally produced precursor peptide, combined with inter‐side‐chain crosslinking through a genetically encoded cysteine‐reactive amino acid. This strategy could be successfully applied to achieve formation of structurally diverse bicyclic peptides with high efficiency and selectivity in Escherichia coli. Insights into the sequence of reactions underlying the peptide bicyclization process were gained from time‐course experiments. Finally, the potential utility of this methodology toward the discovery of macrocyclic peptides with enhanced functional properties was demonstrated through the isolation of a bicyclic peptide with sub‐micromolar affinity for streptavidin.     

Current Views of the Structure of the Mammalian Mitochondrial Ribosome

Mammalian mitochondria synthesize polypeptides crucial for energy generation using ribosomes with a number of unique features. These ribosomes are very protein rich and have very truncated ribosomal RNAs. The bulk of the mammalian mitochondrial ribosome is composed of proteins, only about half of which are homologs of ribosomal proteins found in other translational systems. A number of distinctive features are found in these ribosomes. Among these is a gate-like structure that allows entrance of the primarily leaderless mRNAs that characterize this system. The exit tunnel of the large subunit is also quite unusual and includes a site in which the nascent peptide is visible to solvent prior to the normal exit site. Further, this region of the mitochondrial ribosome is dominated by ribosomal proteins rather than rRNA and is involved in the interaction of the ribosome with the inner membrane where all of the translation products are ultimately located. The proteins of the mitochondrial ribosome appear to play a number of important roles in the cell in addition to their function in protein biosynthesis, including roles in apoptosis and in cell cycle control.     

Differences in the aerosolization behavior of microorganisms as revealed through their transport by biogas

The aerosol microbial diversity of biogas was analyzed in order to examine the aerosolization behavior of microorganisms. Six biogas samples were analyzed: five from mesophilic and thermophilic anaerobic digestors treating different wastes, and one from landfill. Epifluorescent microscopic counts reveal that with 10(6) Prokarya m(-3), only one per one thousand billion were aerosolized from the digestor sludges to the biogas. SSU (Small Sub Unit) ribosomal fingerprinting (Single Strand Conformation Polymorphism) shows that microbial communities in the biogas were not just a rough copy of anaerobic digestor microbial communities and underlines that all microorganisms are not equally convoyed by biogas. To assess the difference occurring in aerosolization, 675 biogas-borne SSU ribosomal DNA were analyzed and compared to published anaerobic digestor microbial diversity. Results show that microorganisms belonging to Archaea, Deltaproteobacteria, Spirochaetes, Thermotogae, Chloroflexi phyla and sulfate-reducing groups were non-aerosolized whereas microorganisms belonging to Alphaproteobacteria, Betaproteobacteria, Gammaproteobacteria, TM7 phyla as well as strictly aerobic and occasionally pathogenic species presented high levels of aerosolization. Finally, microorganisms belonging to Actinobacteria, Firmicutes and Bacteroidetes phyla represent passively-aerosolized microorganisms with similar frequencies in biogas-borne and anaerobic digestor microbial communities.