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ITS exhibited the highest inter to intraspecific K2P distances ratio, followed by trnH-psbA (Figure 3A).

In both Ficus and Gossypium, ITS exhibited the highest interspecific and rbcL and trnH-psbA the lowest intraspecific divergence (Table 1).

In the phylogenetic analysis of Ficus, ITS exhibited 100% species recovery (Figure S5A, Table 2) followed by trnH-psbA (82%) (Figure S5D, Table 2).

However, ITS exhibited high haplotype diversities and low nucleotide diversities in all populations, suggesting population expansion.

ITS exhibited the widest range of pair-wise maximum likelihood distances among species within the genus, ranging from 0.14% – 21.26%.

Analysis of 10 individuals from each of seven geographic regions, encompassing Africa, Asia and Europe, revealed that the genes gdh and ITS exhibited the highest number of polymorphic sites (59%and79%9%, respectively) and most OTUs (defined at 99% identity) were unique to a given country.

DTA analysis of the polyamide 39 exhibited an exothermic peak at 590 °C and its TGA exhibited degradation processes at 205 °C (11.2 % wt loss), 298 °C (3.3 % wt loss), 466 °C (20.9 % wt loss) and 634 °C (65.8 % wt loss) leaving 0%% mass residue.

Interestingly, it was also shown, that the cordierite monolith support on its own exhibited catalytic activity (27% conversion of the triglyceride).

Harmine and its derivatives exhibited remarkable DNA intercalation capacity and significant Topo I inhibition activity but no effect with Topo II.

Our previous studies indicated that 111In-diethylenetriaminepentaacetic acid 111In-DTPA -octreotidee derivatives with an additional negative charge by replacing N-terminal d-phenylalanine (d-Phe) with an acidic amino acid such as l-aspartic acid (Asp) or its derivative exhibited low renal radioactivity levels when compared with 111In-DTPA -octreotideeotide.

According to the annotations and the references in TAIR, NdhL is thought to be a subunit of the Ndh complex and its mutant exhibited weak Ndh activity (Shimizu et al., 2008), CRR7 is considered as an essential factor of Ndh formation, NdhN is a required element for Ndh complex formation, and NdhO appeared to be a factor involved in Ndh complex assembly (Rumeau et al., 2005).