English (United Kingdom)

https://curated-unify.zendy.io/wp-json/zendy-region/v1/featured_content/oa?rat=en

https://curated-unify.zendy.io/wp-json/zendy-region/v1/highlighted_journal/

Global: Zendy Tools annual

Presents the keyphrase highlighting as premium feature

Keyphrase Highlighting

Presents the summarisation as premium feature

Summarisation

Insights

Presents the pdf analysis as premium feature

PDF Analysis

Presents the zaia usage as premium feature

ZAIA

Global: Zendy Tools monthly

Global: Zendy Plus monthly

Presents the access of premium content as premium feature

Premium Content

Global: Zendy Plus annual

Global: Zendy Free Plan

DNA from 59 Beauveria bassiana isolates and one B. brongniartii isolate were subjected to inter-simple-sequence-repeat-anchored polymerase chain reaction (ISSR-PCR) amplification with three short, 14–18-nucleotide primers that included tandemly repeated sequences. ISSR-PCR was found to be highly reproducible since DNA amplification from several single-spore-isolate subcultures of the B. bassiana F-263 isolate resulted in identical banding patterns. Each primer produced highly polymorphic bands, and high gene diversities for each primer were estimated with a range from 0.24 to 0.28. Consequently, all B. bassiana isolates, including F-263, were characterized by unique banding patterns. A dendrogram created by unweighted pair group method analysis (UPGMA) of ISSR-PCR data showed several small clades composed of isolates that originated from the insect order Coleoptera. They were dispersed throughout the dendrogram and did not comprise a large clade. A similar pattern was found for isolates from Lepidoptera and Hymenoptera.

applied entomology and zoology

Characterization of Beauveria bassiana isolates from Japan using inter-simple-sequence-repeat-anchored polymerase chain reaction (ISSR-PCR) amplification