scholarly journals Identification and Characterization of Andalusicin – N-terminally Dimethylated Class III Lantibiotic from Bacillus thuringiensis sv. andalousiensis

iScience ◽  
2021 ◽  
pp. 102480
Author(s):  
Anastasiia Grigoreva ◽  
Julia Andreeva ◽  
Dmitry Bikmetov ◽  
Anastasiia Rusanova ◽  
Marina Serebryakova ◽  
...  
1999 ◽  
Vol 87 (5) ◽  
pp. 640-648 ◽  
Author(s):  
M. Porcar ◽  
J. Iriarte ◽  
V. Cosmao Dumanoir ◽  
M.D. Ferrandis ◽  
M. M. Lecadet ◽  
...  

2022 ◽  
Vol 147 (1) ◽  
pp. 7-17
Author(s):  
Ying Yang ◽  
Xian-Ge Hu ◽  
Bingsong Zheng ◽  
Yue Li ◽  
Tongli Wang ◽  
...  

MicroRNAs (miRNAs) are short noncoding RNAs (20–25 nucleotides) that regulate gene expression posttranscriptionally. However, identification and characterization of miRNAs remain limited for conifer species. In this study, we applied transcriptome-wide miRNAs sequencing to a conifer species Platycladus orientalis, which is highly adaptable to a wide range of environmental adversities, including drought, barren soil, and mild salinity. A total of 17,181,542 raw reads were obtained from the Illumina sequencing platform; 31 conserved and 91 novel miRNAs were identified, and their unique characteristics were further analyzed. Ten randomly selected miRNAs were validated by quantificational real-time polymerase chain reaction. Through miRNA target predictions based on psRNATarget, 2331 unique mRNAs were predicted to be targets of P. orientalis miRNAs that involved in 187 metabolic pathways in KEGG database. These targets included not only important transcription factors (e.g., class III homeodomain leucine zipper targeted by por-miR166d) but also indispensable nontranscriptional factor proteins (i.e., por-miR482a-3p regulated nucleotide-binding site leucine-rich repeat protein). Interestingly, six miRNAs (por-miR16, -miR44, -miR60-5p, -miR69–3p, -miR166b-5p, and -miR395c) were found in adaptation-related pathways (e.g., drought), indicating their possible involved in this species’ stress-tolerance characteristics. The present study provided essential information for understanding the regulatory role of miRNAs in P. orientalis and sheds light on their possible use in tree improvement for stress tolerance.


2015 ◽  
Vol 25 (8) ◽  
pp. 1281-1290 ◽  
Author(s):  
Zhenghong Zhang ◽  
Helong Hao ◽  
Zhongmei Tang ◽  
Zhengzheng Zou ◽  
Keya Zhang ◽  
...  

2013 ◽  
Vol 79 (11) ◽  
pp. 3364-3370 ◽  
Author(s):  
Yunjun Sun ◽  
Qiang Zhao ◽  
Liqiu Xia ◽  
Xuezhi Ding ◽  
Quanfang Hu ◽  
...  

ABSTRACTThe total protoxin complement in the parasporal body of mosquitocidal strain,Bacillus thuringiensissubsp.jegathesan367, was determined by use of a polyacrylamide gel block coupled to mass spectrometry. A total of eight protoxins were identified from this strain, including five reported protoxins (Cry11Ba, Cry19Aa, Cry24Aa, Cry25Aa, and Cyt2Bb), as well as three previously undescribed (Cry30Ca, Cry60Aa, and Cry60Ba) in this isolate. It was interesting that the encoding genes of three new protoxins existed ascry30Ca-gap-orf2andcry60Ba-gap-cry60Aa. Thecry30Caand a downstreamorf2gene were oriented in the same direction and separated by 114 bp, andcry60Bawas located 156 bp upstream from and in the same orientation tocry60Aa. The three new protoxin genes were cloned fromB. thuringiensissubsp.jegathesanand expressed in an acrystalliferous strain under the control ofcyt1Agene promoters and the STAB-SD stabilizer sequence. Recombinant strain containing onlycry30Cadid not produce visible inclusion under microscope observation, while that containing bothcry30Caandorf2could produce large inclusions. Cry60Aa and Cry60Ba synthesized either alone or together in the acrystalliferous host could yield large inclusions. In bioassays using the fourth-instar larvae ofCulex quinquefasciatus, Cry60Aa and Cry60Ba alone or together had estimated 50% lethal concentrations of 2.9 to 7.9 μg/ml; however, Cry30Ca with or without ORF2 was not toxic to this mosquito.


2009 ◽  
Vol 47 (4) ◽  
pp. 431-440 ◽  
Author(s):  
Catiane S. Souza ◽  
Bruno M. Oliveira ◽  
Gustavo G. L. Costa ◽  
Albert Schriefer ◽  
Alessandra Selbach-Schnadelbach ◽  
...  

2006 ◽  
Vol 188 (21) ◽  
pp. 7592-7599 ◽  
Author(s):  
Chi-Ling Tseng ◽  
Hui-Ju Chen ◽  
Gwo-Chyuan Shaw

ABSTRACTA gene that codes for a novel intracellular poly-3-hydroxybutyrate (PHB) depolymerase has now been identified in the genome ofBacillus thuringiensissubsp.israelensisATCC 35646. This gene, previously annotated as a hypothetical 3-oxoadipate enol-lactonase (PcaD) gene and now designatedphaZ, encodes a protein that shows no significant similarity with any known PHB depolymerase. Purified His-tagged PhaZ could efficiently degrade trypsin-activated native PHB granules as well as artificial amorphous PHB granules and release 3-hydroxybutyrate monomer as a hydrolytic product, but it could not hydrolyze denatured semicrystalline PHB. In contrast, purified His-tagged PcaD ofPseudomonas putidawas unable to degrade trypsin-activated native PHB granules and artificial amorphous PHB granules. TheB. thuringiensisPhaZ was inactive againstp-nitrophenylpalmitate, tributyrin, and triolein. Sonication supernatants of the wild-typeB. thuringiensiscells exhibited a PHB-hydrolyzing activity in vitro, whereas those prepared from aphaZmutant lost this activity. ThephaZmutant showed a higher PHB content than the wild type at late stationary phase of growth in a nutrient-rich medium, indicating that this PhaZ can function as a PHB depolymerase in vivo. PhaZ contains a lipase box-like sequence (G-W-S102-M-G) but lacks a signal peptide. A purified His-tagged S102A variant had lost the PHB-hydrolyzing activity. Taken together, these results indicate thatB. thuringiensisharbors a new type of intracellular PHB depolymerase.


1992 ◽  
Vol 6 (9) ◽  
pp. 1211-1217 ◽  
Author(s):  
Ravi Tailor ◽  
Jan Tippett ◽  
Graham Gibb ◽  
Stephen Pells ◽  
Linda Jordan ◽  
...  

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