Water pollution footprints induced by industrial import and export in China

With the rapid development of foreign trade in China, industrial import and export has been an absolute subject in recent years. The huge trade surplus of import and export trade of industrial products brings not only high profits, but also pollution costs as well. Based on the concept of water pollution footprints(WPFs), this study applies the input-output method and calculates pollutant-producing coefficients of 20 major industrial sectors in China and investigates the WPFs caused by the import and export trades of these industrial sectors. The research results show that WPF resulting from exports exceeds that of imports from 2011 to 2015 in China. The net inflow of pollution footprint is mainly from paper mills, printing and stationery manufacturing, and textile industry; whereas a great number of WPFs are transferred to other countries by these sectors,such as metal mining and dressing industry and oil and natural gas exploitation industry.

A novel secreted protein, NISP1, is phosphorylated by soybean Nodulation Receptor Kinase to promote nodule symbiosis

Nodulation Receptor Kinase(NORK) functions as a co-receptor of Nod factor receptors to mediate rhizobial symbiosis in legumes, but its direct phosphorylation substrates that positively mediate root nodulation remain to be fully identified.Here, we identified a GmNORK-Interacting Small Protein(GmNISP1) that functions as a phosphorylation target of GmNORK to promote soybean nodulation. GmNORKα directly interacted with and phosphorylated GmNISP1. Transcription of GmNISP1 was strongly induced after rhizobial infection in soybean roots and nodules. GmNISP1 encodes a peptide containing 90 amino acids with a “DY” consensus motif at its N-terminus.GmNISP1 protein was detected to be present in the apoplastic space. Phosphorylation of GmNISP1 by GmNORKα could enhance its secretion into the apoplast. Pretreatment with either purified GmNISP1 or phosphorylation-mimic GmNISP1~(12D) on the roots could significantly increase nodule numbers compared with the treatment with phosphorylation-inactive GmNISP1~(12A).The data suggested a model that soybean GmNORK phosphorylates GmNISP1 to promote its secretion into the apoplast, which might function as a potential peptide hormone to promote root nodulation.