ライフサイエンスコーパス: Vigna

1 bacum) plants expressing a wild-type form of Vigna aconitifolia P5CS and a mutated form of the enzyme

2 rought-tolerant grain legumes like mothbean (Vigna acontifolia), tepary bean (Phaseolus acutifolius),

3 ly found in elicited seedlings of Phaseolus, Vigna and Lablab, whereas pterocarpans were mainly obser

4 s, including Triticeae and Paniceae grasses, Vigna beans, Dioscorea opposita yam, and Trichosanthes k

5 Nicotiana, Capsicum, Datura, Trigonella, and Vigna, dicot genera that readily regenerate plants from

6 species of tribe Phaseoleae, i.e. Phaseolus, Vigna, Lablab and Psophocarpus, were investigated for in

7 ence of the Glycine genus from the Phaseolus-Vigna lineage and exhibit strong structure-function cons

8 Vigna mungo (blackgram) is an important leguminous pulse

9 ne proteinases (Phaseolus vulgaris EP-C1 and Vigna mungo SHEP) which are also involved in seed storag

10 Thus, the putrescine:polyamine ratio in Vigna protoplasts, which divide readily, is 4-fold lower

11 growth and crop yield, including mung bean [(Vigna radiata (L.) R.

12 yields, especially in crops like mung bean (Vigna radiata (L.) R.

13 L.) Link] in response to different mungbean [Vigna radiata (L.) R.

14 Here, we demonstrated that the symbiosis of Vigna radiata (mung bean) with Bradyrhizobium diazoeffic

15 ons of the mPPases from Thermotoga maritima, Vigna radiata and Clostridium leptum and characterised b

16 Seeds of Oryza sativa, Brassica nigra, Vigna radiata and V. aconitifolia were enclosed in Petri

17 the known CI assembly intermediate CI* from Vigna radiata at 3.9 angstrom resolution.

18 odels of CIII(2), CIV, and SC III(2)+IV from Vigna radiata determined by single-particle cryoEM.

19 e developmental gradients along a mung bean (Vigna radiata L.) hypocotyl of the growth rate, plasma m

20 Mung bean (Vigna radiata L.) is an edible legume seed which has att

21 were isolated from hypocotyls of mung bean (Vigna radiata L.), and pyrophosphate (PPi)- or ATP-depen

22 we isolated a 2022 bp cDNA (VrCDPK-1) from a Vigna radiata lambda gt11 library.

23 ied a 141 bp fragment of DNA from mungbeans (Vigna radiata Rwilcz cv. Berken).

24 Here, using mungbean (Vigna radiata var. radiata) as a test case, we investiga

25 main and alternative pathways in mung bean (Vigna radiata) and soybean (Glycine max) following growt

26 Mungbean (Vigna radiata) is a fast-growing, warm-season legume cro

27 e-angle x-ray scattering study of mung bean (Vigna radiata) primary cell walls was combined with publ

28 measuring phytic acid content in green gram (Vigna radiata) seeds was investigated by Fourier Transfo

29 Mung bean (Vigna radiata) stands as a crucial legume crop in Asia,

30 mmended doses on leguminous plant mung bean (Vigna radiata) under laboratory condition.

31 abidopsis and from another plant, mung bean (Vigna radiata), to ascertain if this mechanism is common

32 uolar H(+)-pyrophosphatase (EC 3.6.1.1) from Vigna radiata.

33 reover, the de novo assembly of a tetraploid Vigna species (V. reflexo-pilosa var. glabra) provides g

34 vo RNA-seq assemblies of 22 accessions of 18 Vigna species and protein sets of Glycine max.

35 uggests that genome size differences between Vigna species are mainly attributable to changes in the

36 ology each with BBI from Phaseolus parvulus, Vigna trilobata and Vigna vexilata.

37 rk protease inhibitor (RbTI) from rice bean (Vigna umbellata).

38 m, Phaseolus vulgaris L., Glycine max L. and Vigna umbellate, are essential ingredients of the local

39 of As in hydrated and fresh roots of cowpea (Vigna unguiculata 'Red Caloona') seedlings exposed to 4

40 nts Macroptilium atropurpureum (siratro) and Vigna unguiculata (cowpea) indicate that nolA is require

41 Assessment of genetic diversity of Vigna unguiculata (L.) Walp (cowpea) accessions using in

42 ortant (priority) CWR, using African cowpea (Vigna unguiculata (L.) Walp.) as a case study.

43 rmation of Zn in various tissues of cowpea ( Vigna unguiculata (L.) Walp.) exposed to ZnO-NPs or ZnCl

44 Cowpea (Vigna unguiculata (L.) Walp.) is one of the most importa

45 Cowpea, Vigna unguiculata (L.) Walp., is one of the most importa

46 th limited genomic resources such as cowpea [Vigna unguiculata (L.) Walp.] (2n = 2x = 22), the use of

47 d sections of developing soybean and cowpea (Vigna unguiculata [L.] Walp) nodules revealed localizati

48 Cowpea (Vigna unguiculata [L.] Walp.) is a major crop for worldw

49 in the infected region of nodules of cowpea (Vigna unguiculata [L.] Walpers cv. Queen Anne Blackeye).

50 ified and characterised four Rca isoforms in Vigna unguiculata cv IT97K-499-35 in vitro: Rca1beta, Rc

51 n, and Zn) in three different pulse species: Vigna unguiculata L.

52 lerance during seedling emergence of cowpea (Vigna unguiculata L. Walp.) in an additive and independe

53 Cowpea (Vigna unguiculata L. Walp.) is a legume crop that is res

54 was validated using the purified recombinant Vigna unguiculata PLD, as well as the PLD from Streptomy

55 stroy up to 50% of 1 ton of harvest cowpea ( Vigna unguiculata) after several months of storage.

56 Staple food crops, including cowpea (Vigna unguiculata) and common bean (Phaseolus vulgaris),

57 study we sought to identify QTLs in cowpea (Vigna unguiculata) consistent across experiments conduct

58 Cowpea (Vigna unguiculata) cultivar B301 is resistant to races S

59 re examined within hydrated roots of cowpea (Vigna unguiculata) exposed to either 20 microM selenite

60 focuses on a diversity panel of 188 cowpea (Vigna unguiculata) genotypes to identify which traits ar

61 Black-eyed pea (Vigna unguiculata) is a legume species widely grown in s

62 nce during emergence of seedlings of cowpea (Vigna unguiculata) line 1393-2-11.

63 Cowpea (Vigna unguiculata) nodules contain three leghemoglobins

64 indirect perception of herbivory in cowpea (Vigna unguiculata) plants attacked by fall armyworm (Spo

65 Cowpea (Vigna unguiculata) responds to Fall armyworm (Spodoptera

66 defense responses, we characterized cowpea (Vigna unguiculata) transcriptome changes following elici

67 the effect of boiling seeds of three cowpea (Vigna unguiculata) varieties on nutrient ileal and total

68 inger millet (Eleusine coracana) and cowpea (Vigna unguiculata) were generally insufficient for adequ

69 h as beans (Phaseolus vulgaris) and cowpeas (Vigna unguiculata), differentiation into bacteroids, whi

70 In cowpea (Vigna unguiculata), fall armyworm (Spodoptera frugiperda

71 ed peptides, originally described in cowpea (Vigna unguiculata), was limited even within the Fabaceae

72 re variables to predict the yield of cowpea (Vigna unguiculata), which is widely grown in central Sud

73 een beans (Phaseolus vulgaris), and cowpeas (Vigna unguiculata), with the recoveries of surrogates ra

74 purpureus; pink, red and white colour hulls Vigna unguiculata).

75 al for the formation of effective nodules on Vigna unguiculata.

76 from Phaseolus parvulus, Vigna trilobata and Vigna vexilata.