Domain structure and expression along the midgut and carcass of peritrophins and cuticle proteins analogous to peritrophins in insects with and without peritrophic membrane

2019 ◽  
Vol 114 ◽  
pp. 1-9 ◽  
Author(s):  
Renata O. Dias ◽  
Christiane Cardoso ◽  
Camila S. Leal ◽  
Alberto F. Ribeiro ◽  
Clélia Ferreira ◽  
...  
BMC Genomics ◽  
2021 ◽  
Vol 22 (1) ◽  
Author(s):  
Benshui Shu ◽  
Yan Zou ◽  
Haikuo Yu ◽  
Wanying Zhang ◽  
Xiangli Li ◽  
...  

Abstract Background Spodoptera frugiperda is a serious pest that causes devastating losses to many major crops, including corn, rice, sugarcane, and peanut. Camptothecin (CPT) is a bioactive secondary metabolite of the woody plant Camptotheca acuminata, which has shown high toxicity to various pests. However, the effect of CPT against S. frugiperda remains unknown. Results In this study, bioassays have been conducted on the growth inhibition of CPT on S. frugiperda larvae. Histological and cytological changes were examined in the midgut of larvae fed on an artificial diet supplemented with 1.0 and 5.0 µg/g CPT. The potential molecular mechanism was explored by comparative transcriptomic analyses among midgut samples obtained from larvae under different treatments. A total of 915 and 3560 differentially expressed genes (DEGs) were identified from samples treated with 1.0 and 5.0 µg/g CPT, respectively. Among the identified genes were those encoding detoxification-related proteins and components of peritrophic membrane such as mucins and cuticle proteins. Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analyses indicated that part of DEGs were involved in DNA replication, digestion, immunity, endocrine system, and metabolism. Conclusions Our results provide useful information on the molecular basis for the impact of CPT on S. frugiperda and for future studies on potential practical application.


Author(s):  
B. G. Demczyk

CoCr thin films have been of interest for a number of years due to their strong perpendicular anisotropy, favoring magnetization normal to the film plane. The microstructure and magnetic properties of CoCr films prepared by both rf and magnetron sputtering have been examined in detail. By comparison, however, relatively few systematic studies of the magnetic domain structure and its relation to the observed film microstructure have been reported. In addition, questions still remain as to the operative magnetization reversal mechanism in different film thickness regimes. In this work, the magnetic domain structure in magnetron sputtered Co-22 at.%Cr thin films of known microstructure were examined by Lorentz transmission electron microscopy. Additionally, domain nucleation studies were undertaken via in-situ heating experiments.It was found that the 50 nm thick films, which are comprised of columnar grains, display a “dot” type domain configuration (Figure 1d), characteristic of a perpendicular magnetization. The domain size was found to be on the order of a few structural columns in diameter.


Author(s):  
E.K. Goo ◽  
R.K. Mishra

Ferroelectric domains are twins that are formed when PZT undergoes a phase transformation from a non-ferroelectric cubic phase to a ferroelectric tetragonal phase upon cooling below ∼375°C.,1 The tetragonal phase is spontaneously polarized in the direction of c-axis, making each twin a ferroelectric domain. Thin foils of polycrystalline Pb (Zr.52Ti.48)03 were made by ion milling and observed in the Philips EM301 with a double tilt stage.


1988 ◽  
Vol 49 (C8) ◽  
pp. C8-1817-C8-1818 ◽  
Author(s):  
S. McVitie ◽  
J. N. Chapman ◽  
S. J. Hefferman ◽  
W. A. P. Nicholson

1988 ◽  
Vol 49 (C8) ◽  
pp. C8-665-C8-666 ◽  
Author(s):  
G. Badurek ◽  
R. Giersig ◽  
R. Grössinger ◽  
A. Veider ◽  
H. Weinfurter

1988 ◽  
Vol 49 (C8) ◽  
pp. C8-589-C8-590
Author(s):  
Y. Luo ◽  
Q. G. Ji ◽  
N. Zhang ◽  
B. S. Han

1988 ◽  
Vol 49 (C8) ◽  
pp. C8-329-C8-330 ◽  
Author(s):  
R. Szymczak ◽  
H. Szymczak ◽  
A. Szewczyk ◽  
J. Zawadzki ◽  
D. Gignoux ◽  
...  

1972 ◽  
Vol 136 (3-4) ◽  
pp. 255-272 ◽  
Author(s):  
J. M. Parker
Keyword(s):  

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