Salicornia bigelovii
is a promising halophytic crop for saline soils in semi-arid regions. This study was designed to characterize isolates of endophytic actinobacteria from
S. bigelovii
roots and evaluate the effects associated with plant growth promotion. Twenty-eight endophytic isolates obtained from surface-sterilized roots of
S. bigelovii
were initially selected based on their production of 1-aminocyclopropane-1-carboxylic acid (ACC) deaminase
in vitro
in a chemically defined medium. Application of
Micromonospora chalcea
UAE1, possessing the highest ACC deaminase activity, to
S. bigelovii
seedlings significantly enhanced the plant growth under gnotobiotic and greenhouse conditions. This was clear from the increases in the dry weight and length of both shoot and root, and seed yield compared to the non-ACC deaminase-producing isolate
Streptomyces violaceorectus
, or control treatment. The growth promotion was also supported by significant increases in the content of photosynthetic pigments and the levels of auxins, but significant decreases in the levels of ACC
in planta
. Under greenhouse conditions,
M. chalcea
recovered from inside the inoculated roots in all samplings (up to 12 weeks post inoculation), suggesting that the roots of healthy
S. bigelovii
are a suitable habitat for the endophytic actinobacterial isolates. Pure cultures of
M. chalcea
were not capable of producing auxins, gibberellic acid, cytokinins or polyamines
in vitro
. This indicates that the growth promotion is most likely to be due to the reduction of the endogenous levels of the stress hormone ethylene. Our findings suggest that growth and yields of
S. bigelovii
can be enhanced by the field application of the endophyte
M. chalcea
UAE1. This study is the first to report potential endophytic non-streptomycete actinobacteria to promote the growth of halophytic plants in semi-arid zones under greenhouse conditions.
The acetohydrazide derivative reacted with carbon electrophiles such as acid chlorides, acetylacetone, ethyl acetoacetate and aromatic aldehydes to give some interesting heterocyclic compounds. The hydrazide derivative reacted with acetophenone which in turn underwent Vielsmeier-Haack reaction. Also, the phthalazinethione has been synthesized and its behavior towards hydrazine hydrate, oxidizing agent and ethyl chloroacetate has been investigated. The newly synthesized compounds were characterized by spectroscopic data. The antimicrobial, the cytotoxic, and the antioxidant activities of some of the synthesized products were evaluated. Some of the tested compounds showed very strong cytotoxic activity with respect to the standard.
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